A. Alié, L. Leclère, M. Jager, C. Dayraud, P. Chang et al., Somatic stem cells express Piwi and Vasa genes in an adult ctenophore: ancient association of « germline genes » with stemness, Dev. Biol, vol.350, pp.183-197, 2011.

A. Alié, T. Hayashi, I. Sugimura, M. Manuel, W. Sugano et al., The ancestral gene repertoire of animal stem cells, Proc. Natl. Acad. Sci. USA, vol.112, issue.51, pp.7093-7100, 2015.

S. Anders and W. Huber, Differential expression analysis for sequence count data, 2010.

. R106, P. G. Balasubramanian, A. Beckmann, U. Warnken, M. Schnölzer et al., Proteome of Hydra nematocyst, J. Biol. Chem, vol.11, issue.10, pp.9672-9681, 2012.

H. Bielen and C. Houart, The Wnt cries many: Wnt regulation of neurogenesis through tissue patterning, proliferation, and asymmetric cell division, Dev. Neurobiol, vol.74, issue.8, pp.772-780, 2014.

H. R. Bode, The head organizer in Hydra, Int J Dev Biol, vol.56, pp.473-478, 2012.

A. M. Boehm and T. C. Bosch, Migration of multipotent interstitial stem cells in hydra, Zoology, vol.115, pp.275-282, 2012.

E. Candal, V. Thermes, J. S. Joly, and F. Bourrat, Medaka as a model system for the characterization of cell cycle regulators: a functional analysis of Ol-GADD45 during early embryogenesis, Mech Dev, vol.131, pp.945-958, 2004.

E. Candal, A. Alunni, V. Thermes, F. Jamen, J. S. Joly et al., Ol-Insm1b, a SNAG family transcription factor involved in cell cycle arrest during medaka development, Dev Biol, vol.309, pp.1-17, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00180070

A. Coste, M. Jager, J. Chambon, and M. Manuel, Comparative study of Hippo pathway genes in cellular conveyor belts of a ctenophore and a cnidarian, EvoDevo, vol.7, p.4, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01286578

C. Dayraud, A. Alié, M. Jager, P. Chang, H. Le-guyader et al., Independent specialisation of myosin II paralogues in muscle vs. non-muscle functions during early animal evolution: a ctenophore perspective, BMC Evol. Biol, vol.12, p.107, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01544486

A. Demilly, P. Steinmetz, E. Gazave, L. Marchand, and M. Vervoort, Involvement of the Wnt/?-catenin pathway in neurectoderm architecture in Platynereis dumerilii, Nat. Comm, vol.4, 1915.

E. Denker, M. Manuel, L. Leclère, H. Le-guyader, and N. Rabet, Ordered progression of nematogenesis from stem cells through differentiation stages in the tentacle bulb of Clytia hemisphaerica (Hydrozoa, Cnidaria), Dev. Biol, vol.315, pp.99-113, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00607196

M. Devès and F. Bourrat, Transcriptional mechanisms of developmental cell cycle arrest: problems and models, Semin Cell Dev Biol, vol.23, pp.290-297, 2012.

D. J. Duffy, G. Plickert, T. Kuenzel, W. Tilmann, and U. Frank, Wnt signaling promotes oral but suppresses aboral structures in Hydractinia metamorphosis and regeneration, Development, vol.137, issue.18, pp.3057-3066, 2010.

C. L. Garcin and S. J. Habib, A comparative perspective on Wnt/?-catenin signalling in cell fate determination, Results Probl. Cell Differ, vol.61, pp.323-350, 2017.

L. Gee, J. Hartig, L. Law, J. Wittlieb, K. Khalturin et al., Betacatenin plays a central role in setting up the head organizer in hydra, Dev. Biol, vol.340, pp.116-124, 2010.

C. Guder, I. Philipp, T. Lengfeld, H. Watanabe, B. Hobmayer et al., The Wnt code: cnidarians signal the way, Oncogene, vol.25, pp.7450-7460, 2006.

C. Guder, S. Pinho, T. G. Nacak, H. A. Schmidt, B. Hobmayer et al., An ancient Wnt-Dickkopf antagonism in Hydra, Development, vol.133, issue.5, pp.901-911, 2006.

G. Hemmrich, K. Khalturin, A. Boehm, M. Puchert, F. Anton-erxleben et al., Molecular signatures of the three stem cell lineages in Hydra and the emergence of stem cell function at the base of multicellularity, Mol Biol Evol, vol.29, pp.3267-3280, 2012.

K. Hensel, T. Lotan, S. M. Sanders, P. Cartwright, and U. Frank, Lineage-specific evolution of cnidarian Wnt ligands, Evol. Dev, vol.16, issue.5, pp.259-269, 2014.

B. Hobmayer, F. Rentzsch, K. Kuhn, C. M. Happel, C. C. Von-laue et al., WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra, Nature, vol.407, issue.6801, pp.186-189, 2000.

G. Holló, Demystification of animal symmetry: symmetry is a response to mechanical forces, Biol. Direct, vol.12, issue.1, p.11, 2017.

M. Jager, E. Quéinnec, H. Le-guyader, and M. Manuel, Multiple Sox genes are expressed in stem cells or in differentiating neuro-sensory cells in the hydrozoan Clytia hemisphaerica, vol.2, p.12, 2011.

M. Jager, C. Dayraud, A. Mialot, E. Quéinnec, H. Le-guyader et al., Evidence for involvement of Wnt signalling in body polarities, cell proliferation, and the neurosensory system in an adult ctenophore, PLoS One, vol.8, issue.12, p.84363, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01544483

J. S. Joly, G. Recher, A. Brombin, K. Ngo, and V. Hartenstein, A conserved developmental mechanism builds complex visual systems in insectes and vertebrates, Curr. Biol, vol.26, issue.20, pp.1001-1009, 2016.

K. Khalturin, F. Anton-erxleben, S. Milde, C. Plötz, J. Wittlieb et al., Transgenic stem cells in Hydra reveal an early evolutionary origin for key elements controlling self-renewal and differentiation, Dev. Biol, vol.309, pp.32-44, 2007.

S. J. Kühl and M. Kühl, On the role of Wnt/?-catenin signaling in stem cells, Biochim Biophys. Acta, vol.1830, pp.2297-2306, 2013.

A. Kusserow, K. Pang, C. Sturm, M. Hrouda, J. Lentfer et al., Unexpected complexity of the Wnt gene family in a sea anemone, Nature, vol.433, pp.156-160, 2005.

P. Lapébie, E. Gazave, A. Ereskovsky, R. Derelle, C. Bézac et al., WNT/beta-catenin signalling and epithelial patterning in the homoscleromorph sponge Oscarella, PLoS One, vol.4, issue.6, p.5823, 2009.

P. Lapébie, C. Borchiellini, and E. Houliston, Dissecting the PCP pathway: one or more pathways?, Bioessays, vol.33, pp.759-768, 2011.

P. Lapébie, A. Ruggiero, C. Barreau, S. Chevalier, P. Chang et al., Differential responses to Wnt and PCP disruption predict expression and developmental function of conserved and novel genes in a cnidarian, PLoS Genet, vol.10, issue.9, p.1004590, 2014.

L. Leclère, M. Jager, C. Barreau, P. Chang, H. Le-guyader et al., Maternally localized germ plasm mRNAs and germ cell/stem cell formation in the cnidarian Clytia, Dev. Biol, vol.364, pp.236-248, 2012.

L. Leclère, M. Bause, C. Sinigaglia, J. Steger, and F. Rentzsch, Development of the aboral domain in Nematostella requires b-catenin and the opposing activities of Six3/6 and Frizzled5/8, Development, vol.143, issue.10, pp.1766-1777, 2016.

S. Leininger, M. Adamski, B. Bergum, C. Guder, J. Liu et al., Developmental gene expression provides clues to relationships between sponge and eumetazoan body plans, Nat. Comm, vol.5, p.3905, 2014.

K. M. Loh, R. Van-amerongen, and R. Nusse, Generating cellular diversity and spatial form: wnt signaling and the evolution of multicellular animals, Dev. Cell, vol.38, issue.6, pp.643-655, 2016.

M. Manuel, Early evolution of symmetry and polarity in metazoan body plans, C. R. Biol, vol.332, pp.184-209, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00594710

H. Marlow, D. Q. Matus, and M. Q. Martindale, Ectopic activation of the canonical wnt signalling pathway affects ectodermal patterning along the primary axis during larval development in the anthozoan Nematostella vectensis, Dev. Biol, vol.380, pp.324-334, 2013.

T. Masuda and T. Ishitani, Context-dependent regulation of the ?-catenin transcriptional complex supports diverse functions of Wnt/?-catenin signaling, J. Biochem, vol.161, issue.1, pp.9-17, 2017.

T. Momose and E. Houliston, Two Oppositely Localised Frizzled RNAs as Axis Determinants in a Cnidarian Embryo, PLoS Biol, vol.5, p.70, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02388291

T. Momose, R. Derelle, and E. Houliston, A maternally localised Wnt ligand required for axial patterning in the cnidarian Clytia hemisphaerica, Development, vol.135, pp.2105-2113, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02115404

T. Momose, Y. Kraus, and E. Houliston, A conserved function for Strabismus in establishing planar cell polarity in the ciliated ectoderm during cnidarian larval development, Development, vol.139, issue.23, pp.4374-4382, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02115399

K. A. Mulligan and B. N. Cheyette, Wnt signalling in vertebrate neural development and function, J. Neuroimmune Pharmacol, vol.7, pp.774-787, 2012.

C. Niehrs, On growth and form: a Cartesian coordinate system of Wnt and BMP signalling specifies bilaterian body axes, Development, vol.137, pp.845-857, 2010.

R. Noelanders and K. Vleminckx, How Wnt signaling builds the brain : bridging development and disease, Neuroscientist, vol.23, issue.3, pp.314-329, 2017.

C. P. Petersen and P. W. Reddien, Wnt signaling and the polarity of the primary body axis, Cell, vol.139, pp.1056-1068, 2009.

G. Plickert, V. Jacoby, U. Frank, W. A. Müller, and O. Mokady, Wnt signaling in hydroid development: formation of the primary body axis in embryogenesis and its subsequent patterning, Dev. Biol, vol.298, pp.368-378, 2006.

G. Plickert, U. Frank, and W. A. Müller, Hydractinia, a pioneering model for stem cell biology and reprogramming somatic cells to pluripotency, Int. J. Dev. Biol, vol.56, issue.6-8, pp.519-534, 2012.

J. F. Ryan and A. D. Baxevanis, Hox, Wnt, and the evolution of the primary body axis : insights from the early-divergent phyla, Biology Direct, vol.2, p.37, 2007.

S. F. Altschul, W. Gish, W. Miller, E. W. Myers, and D. J. Lipman, Basic local alignment search tool, J. Mol. Biol, vol.215, pp.403-410, 1990.

S. Anders and W. Huber, Differential expression analysis for sequence count data, 2010.

, Genome Biol, vol.11, p.106

P. Ax, Multicellular Animals: A new Approach to the Phylogenetic Order in, Nature, 1996.

C. D. Baader, V. Schmid, and P. Schuchert, Characterization of a tropomyosin cDNA from the hydrozoan Podocoryne carnea, FEBS Lett, vol.328, pp.63-66, 1993.

C. D. Baader, P. Schuchert, V. Schmid, R. Heiermann, and G. Plickert, Temporally and spatially restricted expression of a gland cell gene during regeneration and in vitro transdifferentiation in the hydrozoan Podocoryne carnea. Roux's Arch, Dev. Biol, vol.204, pp.164-171, 1995.

C. Bacchiocchi, P. Graceffa, and S. S. Lehrer, Myosin-Induced Movement of ??, ??, and ?? Smooth Muscle Tropomyosin on Actin Observed by Multisite FRET, Biophys. J, vol.86, pp.2295-2307, 2004.

S. Baumgarten, O. Simakov, L. Y. Esherick, Y. J. Liew, E. M. Lehnert et al., The genome of Aiptasia, a sea anemone model for coral symbiosis, Proc. Natl. Acad. Sci, vol.112, pp.11893-11898, 2015.

J. Bergsten, A review of long-branch attraction, Cladistics, vol.21, pp.163-193, 2005.

N. L. Bray, H. Pimentel, P. Melsted, and L. Pachter, Near-optimal probabilistic RNA-seq quantification, Nat. Biotechnol, vol.34, pp.525-527, 2016.

V. Brekhman, A. Malik, B. Haas, N. Sher, and T. Lotan, , 2015.

K. O. Broschat and D. R. Burgess, Low M(r) tropomyosin isoforms from chicken brain and intestinal epithelium have distinct actin-binding properties, J. Biol. Chem, vol.261, pp.13350-13359, 1986.

R. D. Campbell, Elimination of Hydra interstitial and nerve cells by means of colchicine, J. Cell Sci, vol.21, pp.1-13, 1976.

J. T. Cannon, B. C. Vellutini, J. Smith, F. Ronquist, U. Jondelius et al., , 2016.

, Xenacoelomorpha is the sister group to Nephrozoa, Nature, vol.530, pp.89-93

D. M. Chapman, Microanatomy of the cubopolyp, Tripedalia cystophora (Class Cubozoa), 1978.

, Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.31, pp.128-168

J. A. Chapman, E. F. Kirkness, O. Simakov, S. E. Hampson, T. Mitros et al., The dynamic genome of Hydra, Nature, vol.464, pp.592-596, 2010.

F. Chia, H. M. Amerongen, and D. J. Peteya, Ultrastructure of the neuromuscular system of the polyp of Aurelia aurita L., 1758 (Cnidaria, scyphozoa), J. Morphol, vol.180, pp.69-79, 1984.

M. Chiodin, J. G. Achatz, A. Wanninger, and P. Martinez, Molecular architecture of muscles in an acoel and its evolutionary implications, J. Exp. Zool. Part B Mol. Dev. Evol, vol.316, pp.427-439, 2011.

J. E. Clayton, L. W. Pollard, M. Sckolnick, C. S. Bookwalter, A. R. Hodges et al., Fission yeast tropomyosin specifies directed transport of myosin-V along actin cables, Mol. Biol. Cell, vol.25, pp.66-75, 2014.

A. G. Collins, P. Schuchert, A. C. Marques, T. Jankowski, M. Medina et al.,

, Medusozoan phylogeny and character evolution clarified by new large and small subunit rDNA data and an assessment of the utility of phylogenetic mixture models, Syst. Biol, vol.55, pp.97-115

A. Coste, Origine(s) du système nerveux des Métazoaires et évolution des mécanismes liés au contrôle de la prolifération cellulaire : apports de l'étude chez un Cténaire et un Cnidaire, 2015.

A. T. Coulton, D. A. East, A. Galinska-rakoczy, W. Lehman, and D. P. Mulvihill, , 2010.

S. Cranz-mileva, B. Mactaggart, J. Russell, and S. E. Hitchcock-degregori, , 2015.

, Evolutionarily conserved sites in yeast tropomyosin function in cell polarity, transport and contractile ring formation, Biol. Open, vol.4, pp.1040-1051

P. Dehal and J. L. Boore, , 2005.

E. Denker, M. Manuel, L. Leclère, H. Le-guyader, and N. Rabet, Ordered progression of nematogenesis from stem cells through differentiation stages in the tentacle bulb of Clytia hemisphaerica (Hydrozoa, Cnidaria), Dev. Biol, vol.315, pp.99-113, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00607196

L. Eme, , 2011.

A. Esteves, B. Dallagiovanna, and R. Ehrlich, A developmentally regulated gene of Echinococcus granulosus codes for a 15.5-kilodalton polypeptide related to fatty acid binding proteins, Mol. Biochem. Parasitol, vol.58, pp.215-222, 1993.

J. Felsenstein, Cases in which parsimony or compatibility methods will be positively misleading, Syst. Zool, vol.27, pp.401-410, 1978.

S. Fortunato, M. Adamski, B. Bergum, C. Guder, S. Jordal et al., , 2012.

, Genome-wide analysis of the sox family in the calcareous sponge Sycon ciliatum: multiple genes with unique expression patterns, Evodevo, vol.3, p.14

J. Frye, V. A. Klenchin, and I. Rayment, Structure of the tropomyosin overlap complex from chicken smooth muscle: Insight into the diversity of N-terminal recognition, Biochemistry, vol.49, pp.4908-4920, 2010.

W. B. Gladfelter, Structure and function of the locomotory system of Polyorchis montereyensis (Cnidaria, Hydrozoa), Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.23, pp.38-79, 1972.

C. Gooding and C. W. Smith, Tropomyosin Exons as Models for Alternative Splicing, In Tropomysin. Advances in Experimental Medicine and Biology, vol.644, pp.27-42, 2007.

P. Graceffa, Movement of smooth muscle tropomyosin by myosin heads, Biochemistry, vol.38, pp.11984-11992, 1999.

P. Graceffa, Phosphorylation of smooth muscle myosin heads regulates the head-induced movement of tropomyosin, J. Biol. Chem, vol.275, pp.17143-17148, 2000.

D. Gregorio, A. Levine, and M. , Regulation of Ci-tropomyosin-like, a Brachyury target gene in the ascidian, Ciona intestinalis. Development, vol.126, pp.5599-5609, 1999.

H. Gröger, P. Callaerts, W. J. Gehring, and V. Schmid, Gene duplication and recruitment of a specific tropomyosin into striated muscle cells in the jellyfish Podocoryne carnea, J. Exp. Zool, vol.285, pp.378-386, 1999.

P. Gunning, G. O'neill, and E. Hardeman, Tropomyosin-Based Regulation of the Actin Cytoskeleton in Time and Space, Physiol. Rev, vol.88, pp.1-35, 2008.

C. Guzman and C. Conaco, Comparative transcriptome analysis reveals insights into the streamlined genomes of haplosclerid demosponges, Sci. Rep, vol.6, p.18774, 2016.

T. A. Hall, BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT, Nucleic Acids Symp. Ser, vol.41, pp.95-98, 1999.

D. H. Heeley, Phosphorylation of tropomyosin in striated muscle, J. Muscle Res. Cell Motil, vol.34, pp.233-237, 2013.

R. R. Helm and C. W. Dunn, Indoles induce metamorphosis in a broad diversity of jellyfish, but not in a crown jelly (Coronatae), PLoS One, vol.12, 2017.

S. L. Hooper and J. B. Thuma, Invertebrate muscles: muscle specific genes and proteins, Physiol. Rev, vol.85, pp.1001-1060, 2005.

M. Irimia, I. Maeso, P. W. Gunning, J. Garcia-fernandez, and S. W. Roy, Internal and external paralogy in the evolution of tropomyosin genes in metazoans, Mol. Biol. Evol, vol.27, pp.1504-1517, 2010.

T. Ishimoda-takagi and M. Kobayashi, Molecular heterogeneity and tissue specificity of tropomyosin obtained from various bivalves, Comp. Biochem. Physiol. --Part B Comp. Biochem, vol.88, pp.443-452, 1987.

T. Ishimoda-takagi, M. Kobayashi, Y. , and M. , Polymorphism and tissue specificity of scallop tropomyosin, Comp. Biochem. Physiol. -Part B Comp. Biochem, vol.83, pp.515-521, 1986.

K. Iwasaki, K. Kikuchi, D. Funabara, and S. Watabe, cDNA cloning of tropomyosin from the anterior byssus retractor muscle of mussel and its structural integrity from the deduced amino acid sequence, Fish. Sci, vol.63, pp.731-734, 1997.

C. C. Karlik and E. A. Fyrberg, Two Drosophila melanogaster tropomyosin genes: structural and functional aspects, Mol. Cell. Biol, vol.6, pp.1965-1973, 1986.

E. Kayal, B. Bentlage, P. Cartwright, A. A. Yanagihara, D. J. Lindsay et al., Phylogenetic analysis of higher-level relationships within Hydroidolina (Cnidaria: Hydrozoa) using mitochondrial genome data and insight into their mitochondrial transcription, PeerJ, vol.3, p.1403, 2015.

A. J. Kee, P. W. Gunning, and E. C. Hardeman, A cytoskeletal tropomyosin can compromise the structural integrity of skeletal muscle, Cell Motil. Cytoskeleton, vol.66, pp.710-720, 2009.

U. Koziol, A. Costábile, M. F. Domínguez, A. Iriarte, G. Alvite et al., , 2011.

, Developmental expression of high molecular weight tropomyosin isoforms in Mesocestoides corti

. Mol, Biochem. Parasitol, vol.175, pp.181-191

J. E. Kraus, D. Fredman, W. Wang, K. Khalturin, and U. Technau, Adoption of conserved developmental genes in development and origin of the medusa body plan, Evodevo, vol.6, p.23, 2015.

S. Q. Le and O. Gascuel, An improved general amino acid replacement matrix, Mol. Biol. Evol, vol.25, pp.1307-1320, 2008.
URL : https://hal.archives-ouvertes.fr/lirmm-00324106

, Chapitre 4

J. P. Lees-miller and D. M. Helfman, The molecular basis for tropomyosin isoform diversity, BioEssays, vol.13, pp.429-437, 1991.

W. Lehman, C. , and R. , Tropomyosin and the steric mechanism of muscle regulation, In Tropomyosin. Advances in Experimental Medicine and Biology, vol.644, pp.95-109, 2008.

L. Ames, C. Ryan, J. F. Bely, A. E. Cartwright, P. Collins et al., A new transcriptome and transcriptome profiling of adult and larval tissue in the box jellyfish Alatina alata: an emerging model for studying venom, vision and sex, BMC Genomics, vol.17, p.650, 2016.

G. Liu, Y. Zhou, D. Liu, Q. Wang, Z. Ruan et al., Global transcriptome analysis of the tentacle of the Jellyfish Cyanea capillata using deep sequencing and expressed sequence tags: Insight into the toxin-and degenerative disease-related transcripts, PLoS One, vol.10, 2015.

M. S. López-de-haro, L. M. Salgado, C. N. David, and T. C. Bosch, Hydra tropomyosin TROP1 is expressed in head-specific epithelial cells and is a major component of the cytoskeletal structure that anchors nematocytes, J. Cell Sci, vol.107, pp.1403-1411, 1994.

G. O. Mackie, The elementary nervous system revisited, Am. Zool, vol.30, pp.907-920, 1990.

A. Mádi, S. Mikkat, B. Ringel, H. J. Thiesen, and M. O. Glocker, Profiling stagedependent changes of protein expression in Caenorhabditis elegans by mass spectrometric proteome analysis leads to the identification of stage-specific marker proteins, Electrophoresis, vol.24, pp.1809-1817, 2003.

A. Mak, L. B. Smillie, and M. Bárány, Specific phosphorylation at serine-283 of alpha tropomyosin from frog skeletal and rabbit skeletal and cardiac muscle, Proc. Natl. Acad. Sci. U. S. A, vol.75, pp.3588-3592, 1978.

A. C. Marques and A. G. Collins, Cladistic analysis of Medusozoa and cnidarian evolution, Invertebr. Biol, vol.123, pp.23-42, 2004.

J. Mateos, R. Herranz, A. Domingo, J. Sparrow, M. et al., , 2006.

, J. Muscle Res. Cell Motil, vol.27, pp.189-201

R. Maytum, V. Hatch, M. Konrad, W. Lehman, and M. A. Geeves, Ultra short yeast tropomyosins show novel myosin regulation, J. Biol. Chem, vol.283, pp.1902-1910, 2008.

T. H. Meedel and K. E. Hastings, Striated muscle-type tropomyosin in a chordate smooth muscle, ascidian body-wall muscle, J. Biol. Chem, vol.268, pp.6755-6764, 1993.

L. S. Miranda, A. G. Collins, Y. M. Hirano, C. E. Mills, and A. C. Marques, Comparative internal anatomy of Staurozoa (Cnidaria), with functional and evolutionary inferences, PeerJ, vol.4, p.2594, 2016.

L. L. Moroz, K. M. Kocot, M. R. Citarella, S. Dosung, T. P. Norekian et al., , 2014.

S. A. Nichols, B. W. Roberts, D. J. Richter, S. R. Fairclough, and N. King, Origin of metazoan cadherin diversity and the antiquity of the classical cadherin/beta-catenin complex, Proc. Natl. Acad. Sci, vol.109, pp.13046-13051, 2012.

S. Ohno, Evolution by Gene Duplication, 1970.

J. F. Peña, A. Alié, D. J. Richter, L. Wang, N. Funayama et al., , 2016.

K. W. Petersen, Development of coloniality in Hydrozoa, Biology and Systematics of Colonial Organisms, pp.105-139, 1979.

N. R. Polato, J. C. Vera, and I. B. Baums, Gene discovery in the threatened elkhorn coral: 454 sequencing of the Acropora palmata transcriptome, PLoS One, vol.6, 2011.

N. H. Putnam, M. Srivastava, U. Hellsten, B. Dirks, J. Chapman et al., Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization, Science, vol.317, pp.86-94, 2007.

. R-core-team, R: A Language and Environment for Statistical Computing, 2017.

I. B. Rogozin, L. Carmel, M. Csuros, and E. Koonin, Origin and evolution of spliceosomal introns, Biol. Direct, vol.7, p.11, 2012.

G. J. Romanes, Jelly-fish, star-fish, and sea-urchins, being a research on primitive nervous systems, The International Scientific Series, vol.1, pp.1-253, 1885.

Y. Rui, J. Bai, and N. Perrimon, Sarcomere formation occurs by the assembly of multiple latent protein complexes, PLoS Genet, vol.6, 2010.

J. F. Ryan, K. Pang, C. E. Schnitzler, A. Nguyen, R. T. Moreland et al., The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution, vol.342, p.1242592, 2013.

L. V. Salvini-plawen, On the origin and evolution of the lower Metazoa, J. Zool. Syst. Evol. Res, vol.16, pp.40-87, 1978.

S. M. Sanders and P. Cartwright, Patterns of Wnt signaling in the life cycle of Podocoryna carnea and its implications for medusae evolution in Hydrozoa (Cnidaria), Evol. Dev, vol.17, pp.325-336, 2015.

S. M. Sanders, M. Shcheglovitova, and P. Cartwright, Differential gene expression between functionally specialized polyps of the colonial hydrozoan Hydractinia symbiolongicarpus (Phylum Cnidaria), BMC Genomics, vol.15, p.406, 2014.

R. A. Satterlie, Do jellyfish have central nervous systems?, J. Exp. Biol, vol.214, pp.1215-1223, 2011.

R. A. Satterlie, Neuronal control of swimming in jellyfish: a comparative story, Can. J. Zool, vol.80, pp.1654-1669, 2002.

M. Sckolnick, E. B. Krementsova, D. M. Warshaw, and K. M. Trybus, Tropomyosin isoforms bias actin track selection by vertebrate myosin Va, Mol. Biol. Cell, vol.27, pp.2889-2897, 2016.

K. Seipel and V. Schmid, Evolution of striated muscle: Jellyfish and the origin of triploblasty, Dev. Biol, vol.282, pp.14-26, 2005.

C. Shinzato, E. Shoguchi, T. Kawashima, M. Hamada, K. Hisata et al., Using the Acropora digitifera genome to understand coral responses to environmental change, Nature, vol.476, pp.320-323, 2011.

F. Sievers, A. Wilm, D. Dineen, T. J. Gibson, K. Karplus et al., Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega, Mol. Syst. Biol, vol.7, 2011.

P. Simion, H. Philippe, D. Baurain, M. Jager, D. J. Richter et al., A Large and Consistent Phylogenomic Dataset Supports Sponges as the Sister Group to All Other Animals, Curr. Biol, vol.27, pp.958-967, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01681528

C. Sinigaglia, D. Thiel, A. Hejnol, E. Houliston, and L. Leclère, A safer, urea-based in situ hybridization method improves detection of gene expression in diverse animal species, Dev. Biol, vol.434, pp.15-23, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01655963

M. ?liwi?ska, M. Zukowska, D. Borys, and J. Moraczewska, Different positions of tropomyosin isoforms on actin filament are determined by specific sequences of end-to-end overlaps, Cytoskeleton, vol.68, pp.300-312, 2011.

J. Spring, N. Yanze, C. Jösch, A. M. Middel, B. Winninger et al., Conservation of Brachyury, Mef2, and Snail in the myogenic lineage of jellyfish: a connection to the mesoderm of Bilateria, Dev. Biol, vol.244, pp.372-384, 2002.

M. Srivastava, E. Begovic, J. Chapman, N. H. Putnam, U. Hellsten et al., The Trichoplax genome and the nature of placozoans, Nature, vol.454, pp.955-960, 2008.

M. Srivastava, O. Simakov, J. Chapman, B. Fahey, M. E. Gauthier et al., The Amphimedon queenslandica genome and the evolution of animal complexity, Nature, vol.466, pp.720-726, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00519655

A. Stamatakis, RAxML version 8: A tool for phylogenetic analysis and post-analysis of large phylogenies, Bioinformatics, vol.30, pp.1312-1313, 2014.

P. R. Steinmetz, J. E. Kraus, C. Larroux, J. U. Hammel, A. Amon-hassenzahl et al., Independent evolution of striated muscles in cnidarians and bilaterians, Nature, vol.487, p.231, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02115417

I. Straehler-pohl, J. , and G. , Life cycle of Carybdea marsupialis Linnaeus, 1758 (Cubozoa, Carybdeidae) reveals metamorphosis to be a modified strobilation, Mar. Biol, vol.147, pp.1271-1277, 2005.

H. Thiel, The Evolution of Scyphozoa: A review, pp.77-117, 1966.

T. Tobita and T. Ishimodatakagi, Changes of tropomyosin isoforms during development of cross-fertilized sea urchin embryos, Dev Growth Differ, vol.38, pp.209-219, 1996.

T. Tobita, F. Hiraide, J. Miyazaki, and T. Ishimodatakagi, Muscle-type tropomyosin of sea urchin egg increases the actin-binding of nonmuscle-type tropomyosin, J. Biochem, vol.120, pp.922-928, 1996.

S. Toshino, H. Miyake, S. Ohtsuka, A. Adachi, Y. Kondo et al., Monodisc strobilation in Japanese giant box jellyfish Morbakka virulenta (Kishinouye, 1910): a strong implication of phylogenetic similarity between Cubozoa and Scyphozoa, Evol. Dev, vol.17, pp.231-239, 2015.

B. Vrhovski, N. Thézé, and P. Thiébaud, Structure and evolution of tropomyosin genes, In Tropomysin. Advances in Experimental Medicine and Biology, vol.644, pp.6-26, 2008.

T. Wakabayashi, Mechanism of the calcium-regulation of muscle contraction -In pursuit of its structural basis, Proc. Jpn. Acad. Ser. B. Phys. Biol. Sci, vol.91, pp.321-350, 2015.

D. S. Weston and W. M. Kemp, Schistosoma mansoni: Comparison of cloned tropomyosin antigens shared between adult parasites and Biomphalaria glabrata, Exp. Parasitol, vol.76, pp.358-370, 1993.

N. V. Whelan, K. M. Kocot, L. L. Moroz, and K. M. Halanych, Error, signal, and the placement of Ctenophora sister to all other animals, Proc. Natl. Acad. Sci, vol.112, pp.5773-5778, 2015.

R. G. White and D. A. Barton, The cytoskeleton in plasmodesmata: A role in intercellular transport?, J. Exp. Bot, vol.62, pp.5249-5266, 2011.

L. Yamamori, K. Okuizumi, C. Sato, S. Ikeda, and H. Toyohara, Comparison of the Inducing Effect of Indole Compounds on Medusa Formation in Different Classes of Medusozoa, Zoolog. Sci, vol.34, pp.173-178, 2017.

R. Yu and S. Ono, Dual roles of tropomyosin as an F-actin stabilizer and a regulator of muscle contraction in Caenorhabditis elegans body wall muscle, Cell Motil. Cytoskeleton, vol.63, pp.659-672, 2006.

R. W. Zajdel, C. R. Denz, S. Lee, S. Dube, E. Ehler et al., Identification, characterization, and expression of a novel alpha-tropomyosin isoform in cardiac tissues in developing chicken, J. Cell. Biochem, vol.89, pp.427-439, 2003.

F. Zapata, F. E. Goetz, S. A. Smith, M. Howison, S. Siebert et al., Phylogenomic analyses support traditional relationships within Cnidaria, PLoS One, vol.10, pp.1-13, 2015.

, Dkk particulièrement diversifiés dans l'embranchement des cnidaires (voir sous-section 3.6.3)

, D'autres acteurs importants de la mise en place des axes de polarité, identifiés chez les anthozoaires, doivent être caractérisés chez les médusozoaires, notamment dans les plans d'organisation des méduses

. Planulozoa, La voie BMP est impliquée dans la mise en place de l'axe dorso-ventral chez les bilatériens (Meinhardt, 2015), et de l'axe directeur chez les anthozoaires

. Genikhovich, alimentent la question autour d'une acquisition homologue de la bilatéralité chez l'ancêtre des Planulozoa ou bien d'acquisitions convergentes chez les antral à l'échelle des hydrozoaires ; le développement des gonophores s'est déplacé, dans certains lignages, de la partie orale du polype portant les tentacules, vers sa base, voire vers le stolon, alors que dans d'autres on a vu la différenciation de gonozoïdes. Le bourgeonnement des méduses d'Hydroidolina, ainsi que des limnoméduses (par exemple Limnocnida), à partir d'un polype, implique la formation d'un entocodon. Le mode de bourgeonnement des narcoméduses résulte vraisemblablement d'une simplification secondaire, tandis que les trachyméduses ont perdu leur stade polype. Concernant la position de développement des gonophores, seules les espèces du groupe Filifera IV (Bougainvilliidae, Cytaeididae, Oceaniidae, Pandeidae, Rathkeidae), et des espèces de Stylasteridae (groupe Filifera III) présentent, de façon dérivée, des bourgeons médusaires à la base de leurs polypes, Chez ces derniers, les facteurs de transcription Hox participent également à ce processus, 2006.

, Concernant les autres hydrozoaires, on peut envisager des acquisitions indépendantes de différenciation de zoïdes au sein de la colonie entre Filifera I + Filifera II, Filifera III, Siphonophora, et Leptothecata, ou bien une acquisition homologue avec des pertes ultérieures (chez les Aplanulata, via la perte de la colonialité, et chez les Filifera IV, 2010.

, l'hydre, ont été suivis de l'élimination de gènes spécifiques du muscle strié (TPM1b, TPM2b, et probablement une configuration identique pour un gène de MLC, Les dactylozoïdes (polypes défensifs armés de cnidocystes) ont été acquis à de multiples reprises, dans diverses lignées d'hydrozoaires, par convergence, 2010.

C. Le-cas-chez-les-hydractiniidae and ;. Nawrocki, avec maintien de la méduse seulement chez la plupart des espèces de Podocoryna (Miglietta and Cunningham, 2012), et chez les Tubulariidae, avec maintien de la méduse seulement chez des espèces d'Ectopleura (Petersen, 1990; Marques and Migotto, La conservation des gènes TPM1b, TPM2b et MLC1a, 2001.

. Macrocolonia-(leclère, , 2009.

L. Enfin and . Govindarajan, Obelia présente des propriétés anatomiques originales comparées aux autres méduses des Campanulariidae, tel qu'une faible proportion de mésoglée, une absence de velum, une configuration de l'ombrelle convexe au repos et plane pendant les contractions de nage, et une musculature locomotrice constituée de cellules musculaires striées formant des couches entrecroisées (au lieu d'une musculature circulaire monocouche, La caractérisation des gènes TPM et MLC d'Obelia, 1968.

H. Aberle, A. Bauer, J. Stappert, A. Kispert, and R. Kemler, ?-catenin is a target for the ubiquitin-proteasome pathway, EMBO Journal, vol.16, issue.13, pp.3797-3804, 1997.

M. J. Abrams, T. Basinger, W. Yuan, C. Guo, and L. Goentoro, Self-repairing symmetry in jellyfish through mechanically driven reorganization, Proceedings of the National Academy of Sciences of the United States of America, vol.112, p.385, 2015.

M. Adamska, S. M. Degnan, K. M. Green, M. Adamski, A. Craigie et al.,

. Degnan, Wnt and TGF-? expression in the sponge Amphimedon queenslandica and the origin of metazoan embryonic patterning, PLoS ONE, vol.2, issue.10, p.171, 2007.

M. Adamska, C. Larroux, M. Adamski, K. Green, E. Lovas et al., Structure and expression of conserved Wnt pathway components in the demosponge Amphimedon queenslandica, Evolution and Development, vol.12, issue.5, p.307, 2010.

B. L. Aerne, The hydrozoan life cycle : A small secreted protein is involved in specification of the polyp stage, Development Genes and Evolution, vol.206, issue.5, pp.337-343, 1996.

B. L. Aerne, C. D. Baader, and V. Schmid, Life stage and tissue-specific expression of the homeobox gene cnox1-Pc of the hydrozoan Podocoryne carnea, Developmental biology, vol.169, issue.2, pp.547-56, 1995.

A. Alié, L. Leclère, M. Jager, C. Dayraud, P. Chang et al., Somatic stem cells express Piwi and Vasa genes in an adult ctenophore : ancient association of "germline genes" with stemness, Developmental biology, vol.350, issue.1, pp.183-97, 2011.

A. Alié, T. Hayashi, I. Sugimura, M. Manuel, W. Sugano et al., The ancestral gene repertoire of animal stem cells, Proceedings of the National Academy of Sciences of the United States of America, vol.112, pp.7093-100, 2015.

G. J. Allman, A monograph of the gymnoblastic or tubularian hydroids, 484 pp., Published for the Ray Society by Robert Hardwicke, p.135, 1871.

, Chapitre 5

S. F. Altschul, W. Gish, W. Miller, E. W. Myers, and D. J. Lipman, Basic local alignment search tool, Journal of Molecular Biology, vol.215, issue.3, pp.403-410, 1990.

A. Amiel and E. Houliston, Three distinct RNA localization mechanisms contribute to oocyte polarity establishment in the cnidarian Clytia hemisphaerica, Developmental biology, vol.327, issue.1, p.280, 2009.

A. R. Amiel, H. Johnston, T. Chock, P. Dahlin, M. Iglesias et al., A bipolar role of the transcription factor ERG for cnidarian germ layer formation and apical domain patterning, Developmental Biology, vol.430, issue.2, pp.346-361, 2017.
URL : https://hal.archives-ouvertes.fr/inserm-01609347

J. N. Anastas, T. L. Biechele, M. Robitaille, J. Muster, K. H. Allison et al.,

. Moon, A protein complex of SCRIB, NOS1AP and VANGL1 regulates cell polarity and migration, and is associated with breast cancer progression, Oncogene, issue.32, pp.3696-3708, 2012.

P. A. Anderson and G. O. Mackie, Electrically coupled, photosensitive neurons control swimming in a jellyfish, Science, vol.197, issue.4299, 1977.

P. A. Anderson and W. E. Schwab, The organization and structure of nerve and muscle in the jellyfish Cyanea capillata (Coelenterata ; Scyphozoa), Journal of Morphology, vol.170, issue.3, p.47, 1981.

P. A. Anderson and W. E. Schwab, An Epithelial Cell-Free Preparation of the Motor Nerve Net of Cyanea (Coelenterata ; Scyphozoa), The Biological Bulletin, vol.166, issue.2, pp.396-408, 1984.

C. Andrikou and M. I. Arnone, Too many ways to make a muscle : Evolution of GRNs governing myogenesis, Zoologischer Anzeiger, vol.256, pp.2-13, 2014.

L. M. Angerer and R. C. Angerer, Patterning the sea urchin embryo : gene regulatory networks, signaling pathways, and cellular interactions, Current Topics in Developmental Biology, vol.53, pp.159-198, 2003.

M. N. Arai, A Functional Biology of Schyphozoa, vol.32, p.92, 1997.

M. N. Arai, The potential importance of podocysts to the formation of scyphozoan blooms : A review, Hydrobiologia, vol.616, issue.1, pp.241-246, 2009.

R. Augustin, A. Franke, K. Khalturin, R. Kiko, S. Siebert et al., Dickkopf related genes are components of the positional value gradient in Hydra, Developmental Biology, vol.296, issue.1, p.311, 2006.

P. Ax, Multicellular Animals : A new Approach to the Phylogenetic Order in Nature, p.74, 1996.

C. D. Baader, P. Schuchert, V. Schmid, R. Heiermann, and G. Plickert, Temporally and spatially restricted expression of a gland cell gene during regeneration and in vitro transdifferentiation in the hydrozoan Podocoryne carnea, Roux's Archives of Developmental Biology, vol.204, issue.3, pp.164-171, 1995.

P. G. Balasubramanian, A. Beckmann, U. Warnken, M. Schnölzer, A. Schüler et al., Proteome of Hydra nematocyst, Journal of Biological Chemistry, vol.287, issue.13, p.186, 2012.

E. E. Ball, D. C. Hayward, R. Saint, and D. J. Miller, A simple plan -cnidarians and the origins of developmental mechanisms, Nature reviews. Genetics, vol.5, issue.8, p.159, 2004.

R. Barnes, P. Calow, P. Olive, D. Golding, and J. Spicer, The Invertebrates : A Synthesis, 2001.

S. Baumgarten, The genome of Aiptasia, a sea anemone model for coral symbiosis, Proceedings of the National Academy of Sciences, vol.112, issue.38, pp.893-904, 2015.

F. M. Bayer and H. B. Owre, The Free-Living Lower Invertebrates, p.116, 1968.

K. M. Bayha, M. N. Dawson, A. G. Collins, M. S. Barbeitos, and S. H. Haddock, Evolutionary relationships among scyphozoan jellyfish families based on complete taxon sampling and phylogenetic analyses of 18S and 28S ribosomal DNA, Integrative and Comparative Biology, vol.50, issue.3, p.83, 2010.

S. Berking, Generation of bilateral symmetry in Anthozoa : A model, Journal of Theoretical Biology, vol.246, issue.3, p.156, 2007.

S. Berking and K. Herrmann, Compartments in Scyphozoa, International Journal of Developmental Biology, vol.51, issue.3, p.145, 2007.

S. Berking, A newly discovered oxidant defence system and its involvement in the development of Aurelia aurita (Scyphozoa, Cnidaria) : reactive oxygen species and elemental iodine control medusa formation, The International journal of developmental biology, vol.49, issue.8, p.300, 2005.

E. A. Berntson, S. C. France, and L. S. Mullineaux, Phylogenetic Relationships within the Class Anthozoa (Phylum Cnidaria) Based on Nuclear 18S rDNA Sequences, Molecular Phylogenetics and Evolution, vol.13, issue.2, pp.417-433, 1999.

N. J. Berrill, Developmental Analysis of Scyphomedusae, Biological Reviews, vol.24, issue.4, pp.393-409, 1949.

H. B. Bigelow, Reports on the scientific results of the expedition to the eastern tropical Pacific, in charge of Alexander Agassiz, by the U.S. Fish Commission steamer 'Albatross, Memoirs of the Museum of Comparative Zoology at Harvard, vol.37, pp.1-243, 1904.

, Chapitre 5

N. W. Blackstone, K. S. Cherry, and D. H. Van-winkle, The role of polyp-stolon junctions in the redox signaling of colonial hydroids, Hydrobiologia, pp.291-298, 2004.

H. R. Bode, Control of Nematocyte Differentiation in Hydra, vol.12, pp.209-232, 1988.

H. R. Bode, The interstitial cell lineage of hydra : a stem cell system that arose early in evolution, Journal of cell science, vol.109, pp.1155-1164, 1996.

H. R. Bode and C. N. David, Regulation of a Multipotent Stem-Cell, Interstitial Cell of Hydra, Progress in Biophysics & Molecular Biology, vol.33, issue.2, pp.189-206, 1978.

F. Bodo and J. Bouillon, Étude histologique du développement embryonnaire de quelques hydroméduses de Roscoff : Phialidium hemisphaericum (L.), Obelia sp. Péron et Lesueur, Sarsia eximia, vol.9, p.161, 1968.

F. Boero, C. Gravili, P. Pagliara, and S. Piraino, The cnidarian premises of metazoan evolution : from triploblasty, to coelom formation, to metamery, Italian Journal of Zoology, vol.65, p.151, 1998.

F. Boero, J. Bouillon, S. Piraino, and V. Schmid, Asexual reproduction in the Hydrozoa, Reproductive Biology of Invertebrates, vol.11, p.250, 2002.

I. Borisenko, M. Adamski, A. Ereskovsky, and M. Adamska, Surprisingly rich repertoire of Wnt genes in the demosponge Halisarca dujardini, BMC Evolutionary Biology, vol.16, issue.1, p.123, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01456317

J. Bouillon, Hydroméduses de la mer de Bismarck (Papouasie, Nouvelle-Guinée). II. -Limnomedusa, Narcomedusa, Trachymedusa et Laingiomedusa (sous-classe nov.), vol.19, pp.473-483, 1978.

J. Bouillon, Origine et phylogenèse des cnidaires et des hydropolypes-hydroméduses, Annales de la Société royale zoologique de Belgique, vol.111, p.75, 1981.

J. Bouillon, Sur le cycle biologique de Eirene hexanemalis (Goette,1886), (Eirenidae, Leptomedusae, Hydrozoa, Cnidaria), Cahiers de biologie marine, vol.24, p.135, 1983.

J. Bouillon, Essai de classification des Hydropolypes-Hydroméduses (Hydrozoa-Cnidaria), Indo-Malayan Zoology, vol.2, pp.29-243, 1985.

J. Bouillon, Considérations sur le développement des Narcoméduses et sur leur position phylogénétique, Indo-Malayan Zoology, vol.4, pp.189-278, 1987.

J. Bouillon, Classe des Hydrozoaires, Traité de Zoologie, vol.3, p.117, 1995.

J. Bouillon, M. D. Medel, F. Pagès, J. M. Gili, F. Boero et al., Fauna of the Mediterranean Hydrozoa, vol.68, p.189, 2004.

E. Bozler, Sinnes-und nervenphysiologische Untersuchungen an Scyphomedusen, Sinnes-und nervenphysiologische Untersuchungen an Scyphomedusen, pp.37-80, 1926.

V. Brekhman, A. Malik, B. Haas, N. Sher, and T. Lotan, Transcriptome profiling of the dynamic life cycle of the scypohozoan jellyfish Aurelia aurita, BMC Genomics, vol.16, p.375, 2015.

S. T. Brennan, T. K. Lowenstein, and J. Horita, Seawater chemistry and the advent of biocalcification, Geology, vol.32, issue.6, pp.473-476, 2004.

R. H. Brewer, Larval Settling Behavior in Cyanea capillata (Cnidaria : Scyphozoa), vol.150, pp.183-199, 1976.

D. Bridge, C. W. Cunningham, B. Schierwater, R. Desalle, and L. W. Buss, Classlevel relationships in the phylum Cnidaria : evidence from mitochondrial genome structure, Proceedings of the National Academy of Sciences of the United States of America, vol.89, pp.8750-53, 1992.

D. Bridge, C. W. Cunningham, R. Desalle, and L. W. Buss, Class-level relationships in the phylum Cnidaria : molecular and morphological evidence, Molecular Biology and Evolution, vol.12, p.77, 1995.

D. M. Bridge, C. T. Ha, A. Nemir, A. Renden, M. M. Rorick et al., Variations on a theme ? Polyp and medusa development in Podocoryna carnea, Hydrobiologia, issue.1-3, pp.299-307, 2004.

D. L. Brinkman, X. Jia, J. Potriquet, D. Kumar, D. Dash et al., Transcriptome and venom proteome of the box jellyfish Chironex fleckeri, BMC Genomics, vol.16, issue.1, pp.1-15, 2015.

M. Brinkmann, D. Oliver, and U. Thurm, Mechanoelectrical transduction in nematocytes of a hydropolyp (Corynidae), vol.178, pp.125-138, 1976.

W. S. Broecker and T. Takahashi, Calcium carbonate precipitation on the Bahama Banks, Journal of Geophysical Research, vol.71, issue.6, pp.1575-1602, 1966.

W. K. Brooks, The life history of the Hydromedusae : a discussion of the origin of the Medusae and of the significance of metagenesis, Memoirs of the Boston Society of Natural History, vol.3, issue.12, 1886.

W. K. Brooks, The sensory clubs or cordyli of Laodice, Journal of Morphology, vol.10, issue.1, p.113, 1895.

E. N. Browne, The production of new hydranths in Hydra by the insertion of small grafts, Journal of Experimental Zoology, vol.7, issue.1, pp.1-23, 1909.

T. Brunet, A. H. Fischer, P. R. Steinmetz, A. Lauri, P. Bertucci et al., The evolutionary origin of bilaterian smooth and striated myocytes, eLife, 5, e19, vol.154, p.389, 2016.

R. C. Brusca and G. J. Brusca, Sinauer Associates, vol.8, p.185, 2003.

L. W. Buss, C. Anderson, and E. W. Bolton, Muscular Anatomy of the Podocoryna carnea Hydrorhiza, PLoS ONE, vol.8, issue.8, p.221, 2013.

C. A. Byrum, An Analysis of Hydrozoan Gastrulation by Unipolar Ingression, Developmental Biology, vol.240, issue.2, p.171, 2001.

K. M. Cadigan and M. L. Waterman, TCF/LEFs and Wnt signaling in the nucleus, Cold Spring Harbor perspectives in biology, vol.4, p.906, 2012.

K. M. Cadigan, M. P. Fish, E. J. Rulifson, and R. Nusse, Wingless repression of Drosophila frizzled 2 expression shapes the wingless morphogen gradient in the wing, Cell, vol.93, issue.5, pp.767-777, 1998.

Y. Cai, J. D. Schiffbauer, H. Hua, and S. Xiao, Morphology and paleoecology of the late Ediacaran tubular fossil Conotubus hemiannulatus from the Gaojiashan Lagerstätte of southern Shaanxi Province, South China, Precambrian Research, vol.191, issue.1-2, pp.46-57, 2011.

Y. Cai, S. Xiao, H. Hua, and X. Yuan, New material of the biomineralizing tubular fossil Sinotubulites from the late Ediacaran Dengying Formation, South China, Precambrian Research, vol.261, pp.12-24, 2015.

R. D. Campbell, Holdfast Movement in the Hydroid Corymorpha palma : Mechanism of Elongation, The Biological Bulletin, vol.134, issue.1, pp.26-34, 1968.

R. D. Campbell, Statocyst lacking cilia in the coelenterate Corymorpha palma, Nature, vol.238, issue.5358, pp.49-51, 1972.

D. E. Canfield and J. Farquhar, Animal evolution, bioturbation, and the sulfate concentration of the oceans, Proceedings of the National Academy of Sciences, vol.106, issue.20, pp.8123-8127, 2009.

D. E. Canfield, S. W. Poulton, and G. M. Narbonne, Late-Neoproterozoic deep-ocean oxygenation and the rise of animal life, Science, issue.5808, pp.92-95, 2007.

K. S. Carmon and D. S. Loose, Development of a bioassay for detection of Wnt-binding affinities for individual frizzled receptors, Analytical Biochemistry, vol.401, issue.2, pp.288-294, 2010.

D. Carré and C. Carré, Origin of germ cells, sex determination, and sex inversion in medusae of the genus Clytia (Hydrozoa, Leptomedusae) : The influence of temperature, Journal of Experimental Zoology, vol.287, issue.3, pp.233-242, 2000.

P. Cartwright and A. M. Nawrocki, Character evolution in Hydrozoa (phylum Cnidaria), vol.50, p.393, 2010.

P. Cartwright, S. L. Halgedahl, J. R. Hendricks, R. D. Jarrard, A. C. Marques et al., Exceptionally preserved jellyfishes from the Middle Cambria, PLoS ONE, vol.2, issue.10, p.89, 2007.

P. Cartwright, N. M. Evans, C. W. Dunn, A. C. Marques, M. P. Miglietta et al., Phylogenetics of Hydroidolina (Hydrozoa : Cnidaria), vol.88, p.141, 2008.

L. R. Cary, The influence of the marginal sense organs on the rate of regeneration in Cassiopea xamachana, Journal of Experimental Zoology, vol.21, issue.1, pp.1-32, 1916.

D. C. Catling and M. W. Claire, How earth's atmosphere evolved to an oxic state : A status report, Earth and Planetary Science Letters, vol.237, issue.1-2, pp.1-20, 2005.

D. M. Chapman, Co-ordination in a scyphistoma, Integrative and Comparative Biology, vol.5, issue.3, p.18, 1965.

D. M. Chapman, A new type of muscle cell from the subumbrella of Obelia, Journal of the Marine Biological Association of the United Kingdom, vol.48, issue.3, p.394, 1968.

D. M. Chapman, Structure, Histochemistry and Formation of the Podocyst, Journal of the Marine Biological Association of the United Kingdom, vol.48, issue.1, pp.187-208, 1968.

D. M. Chapman, Microanatomy of the cubopolyp, Tripedalia cystophora (Class Cubozoa), Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.31, p.388, 1978.

D. M. Chapman, X-ray microanalysis of selected coelenterate statoliths, Journal of the Marine Biological Association of the United Kingdom, vol.65, issue.3, p.112, 1985.

D. M. Chapman, Microanatomy of the bell rim of Aurelia aurita (Cnidaria : Scyphozoa), Canadian Journal of Zoology, vol.77, issue.1, p.385, 1999.

D. M. Chapman, Development of the tentacles and food groove in the jellyfish Aurelia aurita (Cnidaria : Scyphozoa), Canadian Journal of Zoology, vol.79, issue.4, p.56, 2001.

D. M. Chapman and R. James, Intraepithelial flagella in the medusa of Aurelia aurita (L.), Publications of the Seto Marine Biological Laboratory, vol.20, p.49, 1973.

G. B. Chapman and L. G. Tilney, Cytological studies of the nematocysts of Hydra, 1959.

I. Desmonemes, isorhizas, cnidocils, and supporting structures, vol.5, pp.69-78

J. A. Chapman, The dynamic genome of Hydra, Nature, vol.464, issue.7288, pp.592-96, 2010.

S. Chera, L. Ghila, K. Dobretz, Y. Wenger, C. Bauer et al., Apoptotic cells provide an unexpected source of Wnt3 signaling to drive Hydra head regeneration, Developmental cell, vol.17, issue.2, p.244, 2009.

F. Chia, H. M. Amerongen, and D. J. Peteya, Ultrastructure of the neuromuscular system of the polyp of Aurelia aurita L., 1758 (Cnidaria, scyphozoa), vol.180, p.388, 1920.

C. M. Child, Physiological Polarity and Dominance in the Holdfast System of Corymorpha, The Biological Bulletin, vol.54, issue.1, pp.15-35, 1928.

R. Chiori, M. Jager, E. Denker, P. Wincker, C. Silva et al., Are hox genes ancestrally involved in axial patterning ? Evidence from the hydrozoan Clytia hemisphaerica (Cnidaria), PLoS ONE, vol.4, issue.1, p.384, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00498060

S. J. Cho, Y. Vallès, V. C. Giani, E. C. Seaver, and D. A. Weisblat, Evolutionary dynamics of the Wnt gene family : A lophotrochozoan perspective, Molecular Biology and Evolution, vol.27, issue.7, pp.1645-1658, 2010.

D. Chourrout, Minimal ProtoHox cluster inferred from bilaterian and cnidarian Hox complements, Nature, issue.7103, pp.684-687, 2006.
URL : https://hal.archives-ouvertes.fr/halsde-00315426

J. L. Christian, J. A. Mcmahon, A. P. Mcmahon, and R. T. Moon, Xwnt-8, a Xenopus Wnt-1/int-1-related gene responsive to mesoderm-inducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis, Development, vol.111, issue.4, 1991.

C. Claus, Grundzüge der Zoologia, p.74, 1880.

C. Claus, F. ;-i-xx-pp, . Tempsky, . Prague, . Leipzig et al., Untersuchungen über die Organisation und Entwicklung der Medusen, 96pp., 9 text-figs, 1883.

M. M. Coates, Visual ecology and functional morphology of Cubozoa (Cnidaria), Integrative and comparative biology, vol.43, pp.542-590, 2003.

S. P. Colin and J. H. Costello, Morphology, swimming performance and propulsive mode of six co-occurring hydromedusae, Journal of Experimental Biology, vol.205, issue.3, pp.427-437, 2002.

A. G. Collins, Phylogeny of Medusozoa and the evolution of cnidarian life cycles, Journal of Evolutionary Biology, vol.15, issue.3, pp.418-432, 2002.

A. G. Collins and M. Daly, A new deepwater species of stauromedusae, Lucernaria janetae (Cnidaria, Staurozoa, Lucernariidae), and a preliminary investigation of stauromedusan phylogeny based on nuclear and mitochondrial rDNA data, Biological Bulletin, vol.208, issue.3, pp.221-230, 2005.

A. G. Collins, P. Schuchert, A. C. Marques, T. Jankowski, M. Medina et al., Medusozoan phylogeny and character evolution clarified by new large and small subunit rDNA data and an assessment of the utility of phylogenetic mixture models, Systematic Biology, vol.55, issue.1, p.392, 2006.

R. H. Condon, M. B. Decker, and J. E. Purcell, Effects of low dissolved oxygen on survival and asexual reproduction of scyphozoan polyps (Chrysaora quinquecirrha), Hydrobiologia, vol.451, pp.89-95, 2001.

P. F. Cornelius, Medusa loss in leptolid Hydrozoa (Cnidaria), hydroid rafting, and abbreviated life-cycles among their remote-island faunae : an interim review, Scientia Marina, vol.56, issue.2-3, p.143, 1992.

A. Coste, Origine(s) du système nerveux des Métazoaires et évolution des mécanismes liés au contrôle de la prolifération cellulaire : apports de l'étude chez un Cténaire et un Cnidaire, vol.35, p.187, 2015.

A. Coste, M. Jager, J. Chambon, and M. Manuel, Comparative study of Hippo pathway genes in cellular conveyor belts of a ctenophore and a cnidarian, EvoDevo, vol.7, issue.1, p.4, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01286578

C. M. Cruciat and C. Niehrs, Secreted and transmembrane Wnt inhibitors and activators, Cold Spring Harbor Perspectives in Biology, vol.5, issue.3, p.81, 2013.

D. R. Custance, Light as an inhibitor of strobilation in Aurelia aurita, Nature, vol.204, issue.4964, p.110, 1964.

C. Cutress, An Interpretation of the Structure and Distribution of Cnidae in Anthozoa, Systematic Zoology, vol.4, issue.3, pp.120-137, 1955.

G. B. Cuvier, Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée, p.66, 1817.

D. S. Das, N. Wadhwa, N. Kunj, K. Sarda, B. S. Pradhan et al., Dickkopf homolog 3 (Dkk3) plays a crucial role upstream of Wnt/?-catenin signaling for Sertoli cell mediated regulation of spermatogenesis, Plos ONE, vol.8, issue.5, p.603, 2013.

C. N. David and D. Challoner, Distribution of Interstitial Cells and Differentiating Nematocytes in Nests in Hydra attenuata, American Zoologist, vol.14, issue.2, pp.537-542, 1974.

C. N. David and A. Gierer, Cell cycle kinetics and development of Hydra attenuata. III. Nerve and nematocyte differentiation, Journal of cell science, vol.16, issue.2, pp.359-375, 1974.

C. N. David and S. Murphy, Characterization of interstitial stem cells in hydra by cloning, Developmental Biology, vol.58, issue.2, pp.372-383, 1977.

C. N. David, S. Özbek, P. Adamczyk, S. Meier, B. Pauly et al., Evolution of complex structures : minicollagens shape the cnidarian nematocyst, Trends in Genetics, vol.24, issue.9, pp.431-438, 2008.

M. Davidoff, Über Theilungsvorgänge bei Phialidium variabile Haeckel, vol.98, pp.620-624, 1881.

B. Davidson and M. Levine, Evolutionary origins of the vertebrate heart : Specification of the cardiac lineage in Ciona intestinalis, Proceedings of the National Academy of Sciences of the United States of America, vol.100, pp.469-73, 2003.

C. Dayraud, A. Alié, and M. Jager, Independent specialisation of myosin II paralogues in muscle vs. non-muscle functions during early animal evolution : a ctenophore perspective, BMC Evolutionary Biology, vol.12, issue.1, p.107, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01544486

D. M. De-jong, N. R. Hislop, D. C. Hayward, J. S. Reece-hoyes, P. C. Pontynen et al., Components of both major axial patterning systems of the Bilateria are differentially expressed along the primary axis of a 'radiate' animal, the anthozoan cnidarian Acropora millepora, Developmental Biology, vol.298, issue.2, pp.632-643, 2006.

,. P. De-lamarck, Histoire Naturelle des Animaux sans Vertèbres. Tome 2, 568 pp., Verdière, vol.5, p.67, 1816.

E. Denker, M. Manuel, L. Leclère, H. L. Guyader, and N. Rabet, Ordered progression of nematogenesis from stem cells through differentiation stages in the tentacle bulb of Clytia hemisphaerica (Hydrozoa, Cnidaria), Developmental Biology, vol.315, issue.1, p.311, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00607196

M. Devès, Arrêt de la prolifération cellulaire pendant le développement embryonnaire : étude transcriptionnelle de gènes suppresseurs de tumeurs au cours de la croissance du système nerveux central chez le poisson médaka Oryzias latipes, 2012.

M. Devès and F. Bourrat, Transcriptional mechanisms of developmental cell cycle arrest : Problems and models, Seminars in Cell and Developmental Biology, vol.23, issue.3, p.195, 2012.

M. Dohrmann and G. Wörheide, Dating early animal evolution using phylogenomic data, Scientific reports, vol.7, issue.1, p.91, 2017.

X. Dong, J. A. Cunningham, S. Bengtson, C. Thomas, J. Liu et al., Embryos, polyps and medusae of the Early Cambrian scyphozoan, 2013.

. Olivooides, Proceedings of the Royal Society B : Biological Sciences, vol.280, p.90, 1757.

D. Reis, M. , Y. Thawornwattana, K. Angelis, M. J. Telford et al., Uncertainty in the Timing of Origin of Animals and the Limits of Precision in Molecular Timescales, Current Biology, vol.25, issue.22, pp.2939-2950, 2015.

S. J. Du, S. M. Purcell, J. L. Christian, L. L. Mcgrew, and R. T. Moon, Identification of distinct classes and functional domains of Wnts through expression of wild-type and chimeric proteins in Xenopus embryos, Molecular and cellular biology, vol.15, issue.5, pp.2625-2659, 1995.

D. Duboule, The rise and fall of Hox gene clusters, Development, vol.134, issue.14, pp.2549-2560, 2007.

S. Dudgeon, A. Wagner, J. R. Vai?nys, and L. W. Buss, Dynamics of gastrovascular circulation in the hydrozoan Podocoryne carnea : The one-polyp case, Biological Bulletin, vol.196, issue.1, pp.1-17, 1999.

D. J. Duffy and U. Frank, Modulation of COUP-TF expression in a cnidarian by ectopic Wnt signalling and allorecognition, PLoS ONE, vol.6, issue.4, p.443, 2011.

D. J. Duffy, G. Plickert, T. Kuenzel, W. Tilmann, and U. Frank, Wnt signaling promotes oral but suppresses aboral structures in Hydractinia metamorphosis and regeneration, Development, vol.177, p.280, 2010.

J. Dzik, A. Bali?ski, and Y. Sun, The origin of tetraradial symmetry in cnidarians, Lethaia, vol.50, issue.2, pp.306-321, 2017.

E. D. Hanson, The Origin and Early Evolution of Animals, 670 pp, 1978.

C. Edwards, Contributory Thoughts on Form, Function, Habitat and Classification of Hydroids and Hydromedusae, vol.20, pp.11-22, 1973.

N. Eggers and G. Jarms, The morphogenesis of ephyra in Coronatae (Cnidaria, Scyphozoa), Marine Biology, vol.152, issue.3, p.125, 2007.

J. M. Eichinger and R. A. Satterlie, Organization of the ectodermal nervous structures in medusae : Cubomedusae, Biological Bulletin, vol.226, issue.1, p.111, 2014.

D. M. Emms and S. Kelly, OrthoFinder : solving fundamental biases in whole genome comparisons dramatically improves orthogroup inference accuracy, Genome Biology, vol.16, issue.1, p.157, 2015.

, Chapitre 5

H. Fedders, R. Augustin, and T. C. Bosch, A Dickkopf-3-related gene is expressed in differentiating nematocytes in the basal metazoan Hydra, Development genes and evolution, vol.214, pp.72-80, 2004.

D. E. Ferrier and P. W. Holland, Ancient origin of the Hox gene cluster, Nature Reviews Genetics, vol.2, issue.1, pp.33-38, 2001.

R. Feuda, M. Dohrmann, W. Pett, H. Philippe, O. Rota-stabelli et al., Improved Modeling of Compositional Heterogeneity Supports Sponges as Sister to All Other Animals, Current Biology, vol.27, pp.3864-3870, 2017.

J. R. Finnerty, K. Pang, P. Burton, D. Paulson, and M. Q. Martindale, Origins of bilateral symmetry : Hox and dpp expression in a sea anemone, Science, vol.304, issue.5675, p.160, 2004.

S. A. Fortunato, Gene loss, lineage specific expansions and dynamic expression of developmental transcription factors in calcareous sponges, 2014.

S. A. Fortunato, M. Adamski, O. M. Ramos, S. Leininger, J. Liu et al., Calcisponges have a ParaHox gene and dynamic expression of dispersed NK homeobox genes, Nature, vol.514, issue.7524, p.179, 2014.

G. Fränkel, Der statische Sinn der Medusen, Zeitschrift für Vergleichende Physiologie, vol.2, pp.658-690, 1925.

G. Freeman, The effect of larval age on developmental changes in the polyp prepattern of a hydrozoan planula, Zoology, vol.108, issue.1, pp.55-73, 2005.

H. Frey and R. S. Leuckart, Beiträge zur Kenntniss wirbelloser Thiere mit besonderer Berücksichtigung der Fauna des Norddeutschen Meeres, pp.1-39, 1847.

J. H. Fritzenwanker, M. Saina, and U. Technau, Analysis of forkhead and snail expression reveals epithelial-mesenchymal transitions during embryonic and larval development of Nematostella vectensis, Developmental Biology, vol.275, issue.2, pp.389-402, 2004.

G. Fryer and G. D. Stanley, A Silurian porpitoid hydrozoan from Cumbria, England, and a note on porpitoid relationships, vol.47, pp.1109-1119, 2004.

B. Fuchs, Regulation of Polyp-to-Jellyfish Transition in Aurelia aurita, Current Biology, vol.24, issue.3, p.297, 2014.

R. Gacesa, Gene duplications are extensive and contribute significantly to the toxic proteome of nematocysts isolated from Acropora digitifera (Cnidaria : Anthozoa : Scleractinia), vol.16, p.774, 2015.

S. Galle, N. Yanze, and K. Seipel, The homeobox gene Msx in development and transdifferentiation of jellyfish striated muscle, International Journal of Developmental Biology, vol.49, issue.8, p.151, 2005.

B. Galliot and S. Chera, The Hydra model : Disclosing an apoptosis-driven generator of Wnt-based regeneration, Trends in Cell Biology, vol.20, issue.9, p.280, 2010.

B. Galliot and V. Schmid, Cnidarians as a model system for understanding evolution and regeneration, International Journal of Developmental Biology, vol.46, issue.1, pp.39-48, 2002.

M. Gambill and G. Jarms, Can Aurelia (Cnidaria, Scyphozoa) species be differentiated by comparing their scyphistomae and ephyrae ?, European Journal of Taxonomy, vol.107, issue.1, p.24, 2014.

C. Gambini, La morphogenèse gastrovasculaire de la méduse Aurelia aurita, p.385, 2012.

A. Garm, P. Ekström, M. Boudes, and D. E. Nilsson, Rhopalia are integrated parts of the central nervous system in box jellyfish, Cell and Tissue Research, vol.325, issue.2, p.110, 2006.

A. Garm, Y. Poussart, L. Parkefelt, P. Ekström, and D. E. Nilsson, The ring nerve of the box jellyfish Tripedalia cystophora, Cell and Tissue Research, vol.329, issue.1, pp.147-157, 2007.

A. Garm, I. Hedal, M. Islin, and D. Gurska, Pattern-and contrast-dependent visual response in the box jellyfish Tripedalia cystophora, Journal of Experimental Biology, vol.216, issue.24, pp.4520-4529, 2013.

A. Garm, M. Lebouvier, and D. Tolunay, Mating in the box jellyfish Copula sivickisi -Novel function of cnidocytes, Journal of Morphology, vol.276, issue.9, p.184, 2015.

D. Gauchat, F. Mazet, C. Berney, M. Schummer, S. Kreger et al., Evolution of Antp-class genes and differential expression of Hydra Hox/paraHox genes in anterior patterning, Proceedings of the National Academy of Sciences of the United States of America, vol.97, pp.4493-4498, 2000.

E. Gazave, P. Lapébie, E. Renard, C. Bézac, N. Boury-esnault et al., NK homeobox genes with choanocyte-specific expression in homoscleromorph sponges, Development genes and evolution, vol.218, issue.9, pp.479-489, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00418706

L. Gee, J. Hartig, L. Law, J. Wittlieb, K. Khalturin et al., ?catenin plays a central role in setting up the head organizer in Hydra, Developmental Biology, vol.340, issue.1, pp.116-124, 2010.

C. Gegenbaur, Grundriss der Vergleichenden Anatomie, vol.2, p.74, 1878.

, Chapitre 5

J. F. Gemmill, Notes on Food-Capture and Ciliation in the Ephyrae of Aurelia, Proceedings of the Royal Physical Society, vol.20, p.34, 1920.

G. Genikhovich and U. Technau, On the evolution of bilaterality, Development, vol.144, issue.19, p.162, 2017.

G. Genikhovich, P. Fried, M. M. Prünster, J. B. Schinko, A. F. Gilles et al., Axis Patterning by BMPs : Cnidarian Network Reveals Evolutionary Constraints, vol.10, p.390, 2015.

L. Gershwin, Clonal and population variation in jellyfish symmetry, Journal of the Marine Biological Association of the United Kingdom, vol.79, pp.993-1000, 1999.

L. A. Gershwin, Nematocysts of the Cubozoa, vol.184, pp.1-57, 2006.

S. F. Gilbert and S. R. Singer, Developmental Biology, p.168, 2006.

D. A. Gold, N. Nakanishi, N. M. Hensley, K. Cozzolino, M. Tabatabaee et al., Structural and developmental disparity in the tentacles of the moon jellyfish Aurelia sp, PLoS ONE, vol.1, issue.8, p.189, 2015.

D. A. Gold, N. Nakanishi, N. M. Hensley, V. Hartenstein, and D. K. Jacobs, Cell tracking supports secondary gastrulation in the moon jellyfish Aurelia, Development Genes and Evolution, vol.226, issue.6, pp.383-387, 2016.

R. Golz, Anchorage and retraction of nematocytes in the tentacles of the cubopolyp Carybdea marsupialis are mediated by a species-specific mesogleal support, Cell and Tissue Research, vol.274, issue.1, pp.173-180, 1993.

J. M. González-sancho, O. Aguilera, J. M. García, N. Pendás-franco, C. Peña et al., The Wnt antagonist Dickkopf-1 gene is a downstream target of ?-catenin/TCF and is downregulated in human colon cancer, Oncogene, vol.24, issue.6, pp.1098-1103, 2005.

S. J. Gould, The structure of evolutionary theory, p.95, 1433.

A. F. Govindarajan, F. Boero, and K. M. Halanych, Phylogenetic analysis with multiple markers indicates repeated loss of the adult medusa stage in Campanulariidae (Hydrozoa, Cnidaria), Molecular Phylogenetics and Evolution, vol.38, issue.3, p.394, 2006.

J. Goy, Campagne de la Calypso au large des côtes atlantiques de l'Amérique du Sud (1961-1962) -35. Méduses, Annales de l'Institut Oceanographique, vol.75, pp.263-296, 1979.

C. Gravili, J. Bouillon, A. D'elia, and F. Boero, The life cycle of Gastroblasta raffaelei (Cnidaria, Hydrozoa, Leptomedusae, Campanulariidae) and a review of the genus Gastroblasta, Italian Journal of Zoology, vol.74, issue.4, pp.395-403, 2007.

A. Grienenberger, Tgf-beta signaling acts on a Hox response element to confer specificity and diversity to Hox protein function, Development, vol.130, issue.22, pp.5445-5455, 2003.

H. Gröger and V. Schmid, Nerve net differentiation in medusa development of Podocoryne carnea, Scientia Marina, vol.64, pp.107-116, 2000.

L. T. Gronovius, Acta Helvetica Physico-Mathematico-Anatomico-Botanico-Medica, Societas Physico-Medica Basiliensis, vol.4, 1760.

C. Guder, I. Philipp, T. Lengfeld, H. Watanabe, B. Hobmayer et al., The Wnt code : cnidarians signal the way, Oncogene, vol.25, issue.57, p.173, 2006.

C. Guder, S. Pinho, T. G. Nacak, H. A. Schmidt, B. Hobmayer et al., An ancient Wnt-Dickkopf antagonism in Hydra, Development, vol.171, issue.5, p.311, 2006.

S. Guindon, J. F. Dufayard, V. Lefort, M. Anisimova, W. Hordijk et al., New algorithms and methods to estimate maximum-likelihood phylogenies : Assessing the performance of PhyML 3.0, Systematic Biology, vol.59, issue.3, pp.307-321, 2010.
URL : https://hal.archives-ouvertes.fr/lirmm-00511784

K. S. Habicht, M. Gade, B. Thamdrup, P. Berg, and D. E. Canfield, Calibration of sulfate levels in the Archean ocean, Science, vol.298, issue.5602, pp.2372-2374, 2002.

J. Hadzi, Einige Kapitel aus der Entwicklungsgeschichte von Chrysaora, Arbeiten aus dem Zoologischen Instituten der Universität Wien, 1909.

J. Hadzi, An Attempt to Reconstruct the System of Animal Classification, Systematic Zoology, vol.2, issue.4, pp.145-154, 1953.

E. Haeckel, Allgemeine Entwickelungsgeschichte der Organismen, Generelle Morphologie der Organismen, vol.2, p.149, 1856.

E. Haeckel, Die Gastraea-Theorie, die phylogenetische Classification des Thierreichs und die Homologie der Keimblatter, Jenaische Zeitschrift für Naturwissenschaft, vol.8, p.149, 1874.

L. J. Hale, Contractility and Hydroplasmic Movements in the Hydroid Clytia johnstoni, Journal of Cell Science, vol.101, issue.3, pp.339-350, 1960.

L. J. Hale, Cell Movements, Cell Division and Growth in the Hydroid Clytia Johnstoni, Journal of embryology and experimental morphology, vol.12, pp.517-555, 1964.

T. Hall, BioEdit : a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT, Nucleic Acids Symposium Series, vol.41, pp.95-98, 1999.

O. Hamann, Der Organismus der Hydroidpolypen, Jenaische Zeitschrift für Naturwissenschaft, vol.15, pp.473-544, 1882.

, Chapitre 5

C. Han and S. Uye, Combined effects of food supply and temperature on asexual reproduction and somatic growth of polyps of the common jellyfish Aurelia aurita s.l., Plankton and Benthos Research, vol.5, p.29, 2010.

J. Han, S. Kubota, H. O. Uchida, G. D. Stanley, X. Yao et al., Tiny sea anemone from the Lower Cambrian of China, PLoS ONE, vol.5, issue.10, p.88, 2010.

J. Han, S. Hu, P. Cartwright, F. Zhao, Q. Ou et al., The earliest pelagic jellyfish with rhopalia from Cambrian Chengjiang Lagerstätte, Palaeogeography, Palaeoclimatology, Palaeoecology, vol.449, pp.166-173, 2016.

J. Han, X. Zhang, and T. Komiya, Integrated evolution of cnidarians and oceanic geochemistry before and during the Cambrian explosion, The Cnidaria, vol.87, p.94, 2016.

A. R. Hand and S. Gobel, The Structural Organization of the Septate and Gap Junctions of Hydra, Journal of Cell Biology, vol.52, issue.2, pp.397-408, 1972.

C. W. Hargitt, Recent Experiments on Regeneration, The Biological Bulletin, vol.1, issue.1, pp.27-34, 1897.

C. W. Hargitt, Regeneration in Rhizostoma pulmo, Journal of Experimental Zoology, vol.1, issue.1, pp.73-94, 1904.

K. L. Harmata, E. L. Somova, A. P. Parrin, L. S. Bross, S. L. Glockling et al., Structure and signaling at hydroid polyp-stolon junctions, revisited, vol.4, pp.1087-1093, 2015.

B. Hatschek, Lehrbuch der Zoologie, Eine Morphologische Übersicht des Thierreiches zur Einführung in das Studium dieser Wissenschaft, p.68, 1888.

K. Hausmann and T. Holstein, Sensory receptor with bilateral symmetrical polarity -Cnidocil-nematocyst complex in Craspedacusta, Naturwissenschaften, vol.72, issue.3, pp.145-147, 1985.

V. Haüssermann and G. Försterra, Marine benthic fauna of chilean Patagonia, 1000 pp., Nature in Focus, p.119, 2009.

D. C. Hayward, G. Samuel, P. C. Pontynen, J. Catmull, R. Saint et al.,

. Ball, Localized expression of a dpp/BMP2/4 ortholog in a coral embryo, Proceedings of the National Academy of Sciences of the United States of America, vol.99, pp.8106-8111, 2002.

D. C. Hayward, D. J. Miller, and E. E. Ball, Snail expression during embryonic development of the coral Acropora : Blurring the diploblast/triploblast divide ?, Development Genes and Evolution, vol.214, issue.5, pp.257-260, 2004.

J. He, L. Zheng, W. Zhang, and Y. Lin, Life Cycle Reversal in Aurelia sp.1 (Cnidaria, Scyphozoa), vol.10, p.60, 2015.

R. R. Helm, Evolution and development of scyphozoan jellyfish, Biological Reviews, vol.93, issue.2, p.138, 2018.

R. R. Helm and C. W. Dunn, Indoles induce metamorphosis in a broad diversity of jellyfish, but not in a crown jelly (Coronatae), PLoS ONE, vol.12, issue.12, p.392, 2017.

R. R. Helm, S. Tiozzo, M. K. Lilley, F. Lombard, and C. W. Dunn, Comparative muscle development of scyphozoan jellyfish with simple and complex life cycles, EvoDevo, vol.6, issue.1, p.250, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01153728

W. D. Hendricks, C. A. Byrum, and E. L. Meyer-bernstein, Characterization of Circadian Behavior in the Starlet Sea Anemone, Nematostella vectensis, vol.7, p.843, 2012.

K. Hensel, T. Lotan, S. M. Sanders, P. Cartwright, and U. Frank, Lineage-specific evolution of cnidarian Wnt ligands, Evolution and Development, vol.16, issue.5, p.286, 2014.

O. Hertwig and R. Hertwig, Das Nervensystem und die Sinnesorgane der Medusen, Vogel, p.107, 1878.

T. Hincks, A History of the British Hydroid Zoophytes, 338 pp, 1868.

E. Hirai, On the developmental cycles of Aurelia aurita and Dactylometra pacifica, Bulletin of the Marine Biological Station Asamushi, vol.9, issue.2, p.250, 1958.

Y. M. Hirano, Species of Stauromedusae from Hokkaido, with Notes on Their Metamorphosis (With 12 Text-figures), Journal of the Faculty of Science, Hokkaido University, Series VI. Zoology, vol.24, issue.3, pp.182-201, 1986.

B. Hobmayer, F. Rentzsch, K. Kuhn, C. M. Happel, C. C. Von-laue et al., Wnt signalling molecules act in axis formation in the diploblastic metazoan Hydra, Nature, vol.171, issue.6801, p.241, 2000.

D. K. Hofmann, R. Neumann, and K. Henne, Strobilation, budding and initiation of scyphistoma morphogenesis in the rhizostome Cassiopea andromeda (Cnidaria : Scyphozoa), vol.47, pp.161-176, 1978.

L. Z. Holland, Heads or tails ? Amphioxus and the evolution of anterior-posterior patterning in deuterostomes, Developmental Biology, issue.2, pp.209-228, 2002.

T. Holstein, The morphogenesis of nematocytes in Hydra and Forskalia : an ultrastructural study, Journal of Ultrastructure Research, vol.75, pp.276-290, 1981.

T. Holstein and P. Tardent, An ultrahigh-speed analysis of exocytosis : nematocyst discharge, Science, vol.223, issue.4638, pp.830-833, 1984.

S. Hoppler and R. T. Moon, BMP2/4 and Wnt-8 cooperatively pattern the Xenopus mesoderm, Mechanisms of Development, vol.71, issue.1-2, pp.119-129, 1998.

H. Hori and Y. Satow, Dead-end evolution of the Cnidaria as deduced from 5S ribosomal RNA sequences, Hydrobiologia, vol.216, issue.1, p.76, 1991.

G. A. Horridge, The nervous system of the ephyra larva of Aurellia aurita, Journal of Microscopical Science, vol.97, p.44, 1956.

G. A. Horridge, The Nerves and Muscles of Medusae. V. Double Innervation in Scyphozoa, Journal of Experimental Biology, vol.323, p.286, 1956.

G. A. Horridge, The Nerves and Muscles of Medusae. VI. The Rythm, Journal of Experimental Biology, vol.36, pp.72-91, 1959.

G. A. Horridge, Statocysts of medusae and evolution of stereocilia, Tissue and Cell, vol.1, issue.2, p.111, 1969.

E. Horstmann, Untersuchungen zur Physiologie der Schwimmbewegungen der Scyphomedusen, Pflügers Archiv für die Gesamte Physiologie des Menschen und der Tiere, vol.234, p.49, 1934.

S. Hu, M. Steiner, M. Zhu, B. D. Erdtmann, H. Luo et al., Diverse pelagic predators from the Chengjiang Lagerstätte and the establishment of modern-style pelagic ecosystems in the early Cambrian, Palaeogeography, Palaeoclimatology, Palaeoecology, vol.254, issue.1-2, pp.307-316, 2007.

B. Hudry, M. Thomas-chollier, Y. Volovik, M. Duffraisse, A. Dard et al., Molecular insights into the origin of the Hox-TALE patterning system, eLife, pp.1-24, 2014.

J. P. Huelsenbeck and F. Ronquist, MRBAYES : Bayesian inference of phylogenetic trees, Bioinformatics, vol.17, issue.8, pp.754-755, 2001.

T. H. Huxley, The oceanic Hydrozoa : a description of the Calycophoridae and Physophoridae observed during the voyage of H, the years 1846-1850, with a general introduction, vol.20, 1859.

T. H. Huxley, A manual of the anatomy of invertebrated animals, pp.102-157, 1877.

L. Churchill, , p.74

J. S. Hwang, Nematogalectin, a nematocyst protein with GlyXY and galectin domains, demonstrates nematocyte-specific alternative splicing in Hydra, Proceedings of the National Academy of Sciences of the United States of America, vol.107, p.188, 2010.

L. Hyman, Protozoa through Ctenophora, vol.I, p.150, 1940.

M. Irimia, I. Maeso, P. W. Gunning, J. Garcia-fernandez, and S. W. Roy, Internal and external paralogy in the evolution of tropomyosin genes in metazoans, Molecular Biology and Evolution, vol.27, issue.7, pp.1504-1517, 2010.

K. Ishigaki, Aberrant localization of ?-catenin correlates with overexpression of its target gene in human papillary thyroid cancer, The Journal of clinical endocrinology and metabolism, vol.87, issue.7, pp.3433-3440, 2002.

H. Ishii, T. Ohba, and T. Kobayashi, Effects of low dissolved oxygen on planula settlement, polyp growth and asexual reproduction of Aurelia aurita, Plankton and Benthos Research, vol.3, pp.107-113, 2008.

M. Jager, R. Chiori, A. Alié, C. Dayraud, E. Quéinnec et al., New insights on ctenophore neural anatomy : Immunofluorescence study in Pleurobrachia pileus (Müller, 1776), p.316, 2011.

, , pp.171-187

M. Jager, C. Dayraud, and A. Mialot, Evidence for involvement of Wnt signalling in body polarities, cell proliferation, and the neuro-sensory system in an adult ctenophore, Plos ONE, vol.8, issue.12, p.363, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01544483

G. Jagersten, On the early phylogeny of the Metazoa. The bilaterogastrea theory, Zoologiska bidrag från Uppsala, vol.30, pp.321-354, 1955.

M. Jouiaei, Evolution and diversification of the cnidarian venom system, 2016.

K. Kamm and B. Schierwater, Ancient complexity of the non-Hox ANTP gene complement in the anthozoan Nematostella vectensis. Implications for the evolution of the ANTP superclass, Part B : Molecular and Developmental Evolution, vol.596, p.163, 2006.

K. Kamm, B. Schierwater, W. Jakob, S. L. Dellaporta, and D. J. Miller, Axial Patterning and Diversification in the Cnidaria Predate the Hox System, Current Biology, vol.16, issue.9, p.385, 2006.

P. Kaniewska, S. S.-alon, O. Karako-lampert, O. Hoegh-guldberg, and . Levy, Signaling cascades and the importance of moonlight in coral broadcast mass spawning, eLife, 4, e09, p.991, 2015.

G. Kass-simon, Towards a Neuroethology of Nematocyst Discharge in the Tentacles of Hydra, The Biology of Nematocysts, pp.531-541, 1988.

G. Kass-simon and A. A. Scappaticci, The behavioral and developmental physiology of nematocysts, Canadian Journal of Zoology, vol.80, issue.10, pp.1772-1794, 2002.

K. Kato, M. Aochi, and K. Ozato, Developmental aspects of strobilation in Aurelia aurita, Publication of the Seto Marine Biological Laboratory, vol.20, p.58, 1973.

M. Kaucká, The Planar Cell Polarity pathway drives pathogenesis of chronic lymphocytic leukemia by the regulation of B-lymphocyte migration, Cancer Research, vol.73, issue.5, pp.1491-1501, 2013.

E. Kayal, H. B.-roure, A. G. Philippe, D. V. Collins, and . Lavrov, Cnidarian phylogenetic relationships as revealed by mitogenomics, BMC evolutionary biology, vol.13, issue.1, p.94, 2013.

E. Kayal, B. Bentlage, P. Cartwright, A. A. Yanagihara, D. J. Lindsay et al., Phylogenetic analysis of higher-level relationships within Hydroidolina (Cnidaria : Hydrozoa) using mitochondrial genome data and insight into their mitochondrial transcription, PeerJ, vol.3, p.141, 2015.

I. Kelava, F. Rentzsch, and U. Technau, Evolution of eumetazoan nervous systems : insights from cnidarians, Philosophical Transactions of the Royal Society B : Biological Sciences, vol.370, 1684.

K. Khalturin, F. Anton-erxleben, S. Milde, C. Plötz, J. Wittlieb et al., Transgenic stem cells in Hydra reveal an early evolutionary origin for key elements controlling self-renewal and differentiation, Developmental biology, vol.309, issue.1, p.244, 2007.

C. Kiecker and C. Niehrs, A morphogen gradient of Wnt/?-catenin signalling regulates anteroposterior neural patterning in Xenopus, Development, vol.169, issue.21, pp.4189-4201, 2001.

R. Kikinger and L. Von-salvini-plawen, Development from polyp to stauromedusa in Stylocoronella (Cnidaria : Scyphozoa), vol.75, p.147, 1995.

A. Kikuchi, H. Yamamoto, and A. Sato, Selective activation mechanisms of Wnt signaling pathways, Trends in Cell Biology, vol.19, issue.3, p.169, 2009.

J. Kim, W. Kim, and C. W. Cunningham, A new perspective on lower metazoan relationships from 18S rDNA sequences, Molecular biology and evolution, vol.16, issue.3, pp.423-427, 1999.

N. King, The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans, Nature, issue.7180, pp.783-788, 2008.

P. A. Kirkpatrick and P. R. Pugh, Published for the Linnean Society of London and the Estuarine and Brackish-Water Sciences Association by, vol.29, p.116, 1984.

D. P. Knight, Sclerotization of the perisarc of the calyptoblastic hydroid, Laomedea Flexuosa 1. The identification and localization of dopamine in the hydroid, Tissue and Cell, vol.2, issue.3, pp.467-477, 1970.

O. Koizumi, M. Itazawa, H. Mizumoto, S. Minobe, L. C. Javois et al., Nerve ring of the hypostome in Hydra. I. Its structure, development, and maintenance, Journal of Comparative Neurology, vol.326, issue.1, pp.7-21, 1992.

E. Korschelt and K. Heider, Lehrbuch der vergleichenden Entwicklungsgeschichte der wirbellosen Thiere, vol.1, p.135, 1909.

A. Krämer-eis, L. Feretti, P. H. Schiffer, P. Heger, and T. Wiehe, The common developmental genetic toolkit of bilaterian crown clades after a billion years of divergence, 2016.

P. L. Kramp, Synopsis of the medusae of the world, Journal of the Marine Biological Association of the UK, vol.40, pp.7-469, 1961.

J. E. Kraus, D. Fredman, W. Wang, K. Khalturin, and U. Technau, Adoption of conserved developmental genes in development and origin of the medusa body plan, EvoDevo, vol.6, issue.1, p.386, 2015.

Y. Kraus, J. H. Fritzenwanker, G. Genikhovich, and U. Technau, The blastoporal organiser of a sea anemone, Current Biology, vol.17, issue.20, pp.874-876, 2007.

Y. Kraus, A. Aman, U. Technau, and G. Genikhovich, Pre-bilaterian origin of the blastoporal axial organizer, vol.7, p.390, 2016.

M. Kroiher, B. Siefker, and S. Berking, Induction of segmentation in polyps of Aurelia aurita (Scyphozoa, Cnidaria) into medusae and formation of mirror-image medusa anlagen, The International journal of developmental biology, vol.44, issue.5, p.133, 2000.

V. E. Krupnik, Functional and structural diversity of the human Dickkopf gene family, Gene, vol.238, issue.2, pp.301-314, 1999.

S. Kubota, The Life-History of Clytia edwardsi (Hydrozoa ; Campanulariidae) in Hokkaido, Journal of the Faculty of Science, Hokkaido University, Series VI. Zoology, vol.21, issue.3, pp.317-354, 1978.

M. Kühl, L. C. Sheldahl, M. Park, J. R. Miller, and R. T. Moon, The Wnt/Ca2+ pathway : A new vertebrate Wnt signaling pathway takes shape, Trends in Genetics, vol.16, issue.7, pp.279-283, 2000.

S. J. Kühl and M. Kühl, On the role of Wnt/?-catenin signaling in stem cells, Biochimica et biophysica acta, vol.1830, issue.2, pp.2297-306, 2013.

, Chapitre 5

A. Kühn, Die Entwicklung der Geschlechtsindividuen der Hydromedusen, Zoologische Jahrbücher : Abteilung für Anatomie und Ontogenie der Tiere, vol.30, pp.43-174, 1910.

S. Kumburegama, N. Wijesena, R. Xu, and A. H. Wikramanayake, Strabismus-mediated primary archenteron invagination is uncoupled from Wnt/?-catenin-dependent endoderm cell fate specification in Nematostella vectensis (Anthozoa, Cnidaria) : Implications for the evolution of gastrulation, EvoDevo, vol.2, issue.1, p.174, 2011.

L. R. Kump, The rise of atmospheric oxygen, Nature, issue.7176, pp.277-278, 2008.

K. Kuroda, S. Kuang, M. M. Taketo, and M. A. Rudnicki, Canonical Wnt signaling induces BMP4 to specify slow myofibrogenesis of fetal myoblasts, Skeletal muscle, vol.3, 2013.

A. Kusserow, Unexpected complexity of the Wnt gene family in a sea anemone, Nature, vol.282, issue.7022, p.283, 2005.

S. Labeit, S. Lahmers, C. Burkart, C. Fong, M. Mcnabb et al., Expression of Distinct Classes of Titin Isoforms in Striated and Smooth Muscles by Alternative Splicing, and Their Conserved Interaction with Filamins, Journal of Molecular Biology, vol.362, issue.4, pp.664-681, 2006.

J. V. Lamouroux, Extrait d'un mémoire sur la classification des polypes coralligènes non entièrement pierreux, Nouveau Bulletin des Sciences par la Société Philomatique de Paris, vol.3, issue.5, pp.181-188, 1812.

J. V. Lamouroux, J. G. Bory-de-saint-vincent, and E. E. Deslongchamps, Encyclopédie Méthodique. Tome Second, Histoire Naturelle des Zoophytes ou Animaux Rayonnés, 819 pp., chez Mme veuve Agasse, p.66, 1824.

Y. Landesman and S. Y. Sokol, Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain, Mechanisms of Development, vol.63, issue.2, pp.199-209, 1997.

R. Lankester, Embryology and Classification, Quarterly Journal of Microscopical Science, vol.17, 1877.

P. Lapébie, C. Borchiellini, and E. Houliston, Dissecting the PCP pathway : one or more pathways ? : Does a separate Wnt-Fz-Rho pathway drive morphogenesis ?, BioEssays : news and reviews in molecular, cellular and developmental biology, vol.33, issue.10, pp.759-68, 2011.

P. Lapébie, A. Ruggiero, C. Barreau, S. Chevalier, P. Chang et al., Differential Responses to Wnt and PCP Disruption Predict Expression and Developmental Function of Conserved and Novel Genes in a Cnidarian, PLoS Genetics, vol.10, issue.9, p.292, 2014.

F. Lapraz, L. Besnardeau, and T. Lepage, Patterning of the dorsal-ventral axis in echinoderms : Insights into the evolution of the BMP-chordin signaling network, PLoS Biology, vol.7, issue.11, p.248, 1000.

M. Larkin, ClustalW and ClustalX version 2, Bioinformatics, issue.21, pp.2947-2948, 2007.

C. Larroux, B. Fahey, S. M. Degnan, M. Adamski, D. S. Rokhsar et al., The NK Homeobox Gene Cluster Predates the Origin of Hox Genes, Current Biology, vol.17, issue.8, p.179, 2007.

G. Laska-mehnert, Cytologische Veränderungen während der Metamorphose des Cubopolypen Tripedalia cystophora (Cubozoa, Carybdeidae) in die Meduse, Helgoländer Meeresuntersuchungen, vol.39, issue.2, pp.129-164, 1985.

S. Q. Le and O. Gascuel, An improved general amino acid replacement matrix, Molecular Biology and Evolution, vol.25, issue.7, p.307, 2008.
URL : https://hal.archives-ouvertes.fr/lirmm-00324106

L. Gouar, M. , A. Guillou, and M. Vervoort, Expression of a SoxB and a Wnt2/13 gene during the development of the mollusc Patella vulgata, Development Genes and Evolution, vol.214, issue.5, pp.250-256, 2004.

L. Leclère and F. Rentzsch, RGM Regulates BMP-Mediated Secondary Axis Formation in the Sea Anemone Nematostella vectensis, Cell Reports, vol.9, issue.5, p.390, 2014.

L. Leclère, P. Schuchert, and M. Manuel, Phylogeny of the Plumularioidea (Hydrozoa, Leptothecata) : Evolution of colonial organisation and life cycle, Zoologica Scripta, vol.36, issue.4, p.295, 2007.

L. Leclère, P. Schuchert, C. Cruaud, A. Couloux, and M. Manuel, Molecular phylogenetics of Thecata (Hydrozoa, Cnidaria) reveals long-term maintenance of life history traits despite high frequency of recent character changes, Systematic biology, vol.58, issue.5, p.394, 2009.

L. Leclère, M. Jager, C. Barreau, P. Chang, H. L. Guyader et al., Maternally localized germ plasm mRNAs and germ cell/stem cell formation in the cnidarian, 2012.

. Clytia, Developmental biology, vol.364, issue.2, pp.236-284

L. Leclère, M. Bause, C. Sinigaglia, J. Steger, and F. Rentzsch, Development of the aboral domain in Nematostella requires ?-catenin and the opposing activities of six3/6 and frizz-led5, Development, vol.8, pp.1766-1777, 2016.

P. N. Lee, K. Pang, D. Q. Matus, and M. Q. Martindale, A WNT of things to come : Evolution of Wnt signaling and polarity in cnidarians, Seminars in Cell and Developmental Biology, vol.17, p.311, 2006.

S. Leininger, Developmental gene expression provides clues to relationships between sponge and eumetazoan body plans, Nature communications, vol.5, p.278, 2014.

T. Lengfeld, Multiple Wnts are involved in Hydra organizer formation and regeneration, Developmental biology, vol.330, issue.1, p.281, 2009.

J. L. Leonard, The Dkk3 gene encodes a vital intracellular regulator of cell proliferation, PLoS ONE, vol.12, issue.7, p.724, 2017.

J. Lerner, S. A. Mellen, I. Waldron, and R. M. Factor, Neural redundancy and regularity of swimming beats in scyphozoan medusae, Journal of Experimental Biology, vol.55, issue.1, pp.177-84, 1971.

O. Lespinet, A. J. Nederbragt, M. Cassan, W. J. Dictus, A. E. Van-loon et al., Characterization of two snail genes in the gastropod mollusk Patella vulgata. Implications for understanding the ancestral function of the snail-related genes in Bilateralia, Development genes and evolution, vol.212, pp.186-195, 2002.

R. P. Lesson, Histoire Naturelle des Zoophytes. Acalèphes, Roret, issue.3, 1843.

K. G. Leuckart, Ueber den Polymorphismus der Individuen oder die Erscheinungen der Arbeitstheilung in der Natur, Ein Beitrag zur Lehre vom Generationswechsel, 1851.

K. G. Leuckart, Beiträge zur Kenntniss der Medusenfauna von Nizza, vol.22, 1856.

L. A. Levin, Oxygen minimum zone benthos : adaptation and community response to hypoxia, Oceanography and Marine Biology, An Annual Review, vol.41, pp.1-45, 2003.

C. Lewis and T. A. Long, Courtship and reproduction in Carybdea sivickisi (Cnidaria : Cubozoa), vol.147, p.116, 2005.

L. Ames, C. , J. F. Ryan, A. E. Bely, P. Cartwright et al., A new transcriptome and transcriptome profiling of adult and larval tissue in the box jellyfish Alatina alata : an emerging model for studying venom, vision and sex, BMC Genomics, vol.17, issue.1, p.386, 2016.

H. F. Ling, X. Chen, D. Li, D. Wang, G. A. Shields-zhou et al., Cerium anomaly variations in Ediacaran-earliest Cambrian carbonates from the Yangtze Gorges area, South China : Implications for oxygenation of coeval shallow seawater, Precambrian Research, vol.225, pp.110-127, 2013.

C. Linnaeus, Systema Naturae, vol.1, 1758.

A. G. Liu, J. J. Matthews, L. R. Menon, D. Mcilroy, and M. D. Brasier, Haootia quadriformis n. gen., n. sp., interpreted as a muscular cnidarian impression from the Late Ediacaran period (approx. 560 Ma), Proceedings of the Royal Society B : Biological Sciences, vol.281, 1793.

C. Liu, Z. Gu, M. Xing, Y. Sun, S. Chen et al., Sex determination and differentiation in Aurelia sp.1 : the absence of temperature dependence, Chinese Journal of Oceanology and Limnology, pp.1-8, 2014.

F. Liu, Wnt/?-catenin signaling directs multiple stages of tooth morphogenesis, Developmental Biology, vol.313, issue.1, pp.210-224, 2008.

G. Liu, Y. Zhou, D. Liu, Q. Wang, Z. Ruan et al., Global transcriptome analysis of the tentacle of the Jellyfish Cyanea capillata using deep sequencing and expressed sequence tags : Insight into the toxin-and degenerative disease-related transcripts, PLoS ONE, vol.10, issue.11, p.386, 2015.

C. H. Lucas, D. W. Williams, J. A. Williams, and M. Sheader, Seasonal Dynamics and Production of the Hydromedusan Clytia hemisphaerica, 1995.

S. Water, Estuaries, vol.18, issue.2, pp.362-372

O. Maas, Die Scyphomedusen der Siboga-Expedition, Siboga-Expeditie Monographes, vol.11, issue.111, pp.1-91, 1903.

G. O. Mackie, Central Neural Circuitry in the Jellyfish Aglantha : A Model 'Simple Nervous System, vol.13, p.105, 2004.

G. O. Mackie and R. W. Meech, Central circuitry in the jellyfish Aglantha digitale. I. The relay system, Journal of Experimental Biology, vol.198, pp.2261-2270, 1995.

J. Macrander, M. Broe, and M. Daly, Tissue-Specific Venom Composition and Differential Gene Expression in Sea Anemones, Genome biology and evolution, vol.8, issue.8, pp.2358-2375, 2016.

C. R. Magie, M. Daly, and M. Q. Martindale, Gastrulation in the cnidarian Nematostella vectensis occurs via invagination not ingression, Developmental Biology, vol.305, issue.2, p.246, 2007.

M. Manuel, Early evolution of symmetry and polarity in metazoan body plans, Comptes Rendus -Biologies, vol.332, issue.2-3, p.156, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00594710

M. Manuel and Y. L. Parco, Homeobox gene diversification in the calcareous sponge, Sycon raphanus, Molecular Phylogenetics and Evolution, vol.17, issue.1, pp.97-107, 2000.

G. M. Mapstone, Global diversity and review of Siphonophorae (Cnidaria : Hydrozoa), vol.9, pp.1-37, 2014.

, Chapitre 5

H. Marlow, D. Q. Matus, and M. Q. Martindale, Ectopic activation of the canonical Wnt signaling pathway affects ectodermal patterning along the primary axis during larval development in the anthozoan Nematostella vectensis, Developmental biology, vol.380, issue.2, p.175, 2013.

H. Marlow, M. A. Tosches, R. Tomer, P. R. Steinmetz, A. Lauri et al., Larval body patterning and apical organs are conserved in animal evolution, BMC biology, vol.12, 2014.

H. Q. Marlow, M. Srivastava, D. Q. Matus, D. Rokhsar, and M. Q. Martindale, Anatomy and development of the nervous system of Nematostella vectensis, an anthozoan cnidarian, Developmental Neurobiology, vol.69, issue.4, pp.235-254, 2009.

M. M. Maronna, T. P. Miranda, Á. L. Cantero, M. S. Barbeitos, and A. C. Marques, Towards a phylogenetic classification of Leptothecata (Cnidaria, Hydrozoa), vol.6, p.75, 2016.

A. C. Marques and A. G. Collins, Cladistic analysis of Medusozoa and cnidarian evolution, Invertebrate Biology, vol.123, issue.1, p.124, 2004.

A. C. Marques and A. E. Migotto, Cladistic analysis and new classification of the family Tubulariidae (Hydrozoa, Anthomedusae), Papéis Avulsos de Zoologia, vol.41, pp.465-488, 2001.

A. C. Marques, J. García, and C. L. Ames, Internal fertilization and sperm storage in cnidarians : A response to Orr and Brennan, Trends in Ecology and Evolution, vol.30, issue.8, pp.435-436, 2015.

E. Marshman, C. Booth, and C. S. Potten, The intestinal epithelial stem cell, BioEssays, vol.24, issue.1, pp.91-98, 2002.

L. Martell, E. Ciavolino, C. Gravili, S. Piraino, and F. Boero, Population dynamics of the non-indigenous hydrozoan Clytia hummelincki (Hydrozoa : Campanulariidae) in two contrasting Mediterranean habitats, Marine Biology Research, vol.13, issue.5, pp.551-559, 2017.

V. J. Martin, Reorganization of the Nervous System during Metamorphosis of a Hydrozoan Planula, Invertebrate Biology, vol.119, issue.3, pp.243-253, 2000.

V. J. Martin, Photoreceptors of cnidarians, Canadian Journal of Zoology, vol.80, issue.10, pp.1703-1722, 2002.

M. Q. Martindale and J. Q. Henry, Intracellular fate mapping in a basal metazoan, the ctenophore Mnemiopsis leidyi, reveals the origins of mesoderm and the existence of indeterminate cell lineages, Developmental Biology, vol.214, issue.2, pp.243-257, 1999.

R. M. Marx, The Development of the Nervous System of Aurelia aurita (Scyphozoa, Coelenterata), vol.44, p.286, 1997.

T. Masuda and T. Ishitani, Context-dependent regulation of the ?-catenin transcriptional complex supports diverse functions of Wnt/?-catenin signaling, Journal of Biochemistry, vol.161, issue.1, pp.9-17, 2017.

L. M. Masuda-nakagawa, H. Gröer, B. L. Aerne, and V. Schmid, The Hox-like gene Cnox2-Pc is expressed at the anterior region in all life cycle stages of the jellyfish Podocoryne carnea, Development genes and evolution, vol.210, pp.151-156, 2000.

S. Matsakis, Ammonia excretion rate of Clytia spp. hydromedusae (Cnidaria, Thecata) : effects of individual dry weight, temperature and food availability, Marine Ecology Progress Series, vol.87, issue.1, pp.55-63, 1992.

A. Matsuno and T. Hisamatu, Electron Microscopy on Striated Muscles in the Ephyra of Aurelia aurita, Memoirs of the Faculty of Science, vol.16, p.390, 1982.

A. Matsuno and S. Kawaguti, An ultrastructural study of the polyp and strobila of Atorella japonica (Cnidaria, Coronatae) with respect to muscles and nerves, Hydrobiologia, issue.1, pp.39-43, 1991.

D. Q. Matus, K. Pang, H. Marlow, C. W. Dunn, G. H. Thomsen et al., Molecular evidence for deep evolutionary roots of bilaterality in animal development, Proceedings of the National Academy of Sciences of the United States of America, vol.103, issue.30, 2006.

D. Q. Matus, G. H. Thomsen, and M. Q. Martindale, Dorso/ventral genes are asymmetrically expressed and involved in germ-layer demarcation during cnidarian gastrulation, Current Biology, vol.16, issue.5, p.284, 2006.

A. G. Mayer, Medusae of the World, vol.735, p.116, 1910.

L. L. Mcgrew, A. P. Otte, and R. T. Moon, Analysis of Xwnt-4 in embryos of Xenopus laevis : a Wnt family member expressed in the brain and floor plate, Development, vol.115, issue.2, pp.463-73, 1992.

A. P. Mcmahon and A. Bradley, The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain, Cell, vol.62, issue.6, pp.1073-1085, 1990.

H. Meinhardt, Models for patterning primary embryonic body axes : The role of space and time, Seminars in Cell and Developmental Biology, vol.42, p.390, 2015.

O. Mendivil-ramos, D. Barker, and D. E. Ferrier, Ghost loci imply Hox and ParaHox existence in the last common ancestor of animals, Current Biology, vol.22, issue.20, p.179, 2012.

M. A. Mendoza-becerril, J. E. Marian, A. E. Migotto, and A. C. Marques, Exoskeletons of Bougainvilliidae and other Hydroidolina (Cnidaria, Hydrozoa) : structure and composition, vol.5, p.2964, 2017.

, Chapitre 5

E. Metschnikoff, Zur Entwickelungsgeschichte der Kalkschwämme, Zeitschrift für wissenschaftliche Zoologie, vol.24, pp.1-14, 1874.

E. Metschnikoff, Embryologische Studien an Medusen : Ein Beitrag zur Genealogie der Primitiv-organe, A. Holder, 1886.

M. P. Miglietta and C. W. Cunningham, Evolution of life cycle, colony morphology, and host specificity in the family Hydractiniidae (Hydrozoa, Cnidaria), Evolution, p.393, 2012.

M. Miljkovic-licina, D. Gauchat, and B. Galliot, Neuronal evolution : Analysis of regulatory genes in a first-evolved nervous system, the Hydra nervous system, BioSystems, vol.76, issue.1-3, pp.75-87, 2004.

M. Miljkovic-licina, S. Chera, L. Ghila, and B. Galliot, Head regeneration in wildtype Hydra requires de novo neurogenesis, Development, vol.134, issue.6, pp.1191-1201, 2007.

S. Minobe, K. Fei, L. Yan, M. P. Sarras, and M. J. Werle, Identification and characterization of the epithelial polarity receptor 'Frizzled' in Hydra vulgaris, Development Genes and Evolution, vol.210, issue.5, pp.258-262, 2000.

L. S. Miranda, A. G. Collins, and A. C. Marques, Molecules clarify a cnidarian life cycle -The "Hydrozoan" Microhydrula limopsicola is an early life stage of the staurozoan Haliclystus antarcticus, PLoS ONE, vol.5, issue.4, pp.1-9, 2010.

L. S. Miranda, A. G. Collins, and A. C. Marques, Internal anatomy of Haliclystus antarcticus (Cnidaria, Staurozoa) with a discussion on histological features used in staurozoan taxonomy, Journal of Morphology, vol.274, issue.12, p.123, 2013.

L. S. Miranda, A. G. Collins, Y. M. Hirano, C. E. Mills, and A. C. Marques, Comparative internal anatomy of Staurozoa (Cnidaria), with functional and evolutionary inferences, PeerJ, vol.4, p.287, 2016.

O. Mokady, M. H. Dick, D. Lackschewitz, B. Schierwater, and L. W. Buss, Over one-half billion years of head conservation ? Expression of an ems class gene in Hydractinia symbiolongicarpus (Cnidaria : Hydrozoa), Proceedings of the National Academy of Sciences of the United States of America, vol.95, p.156, 1998.

T. Momose and E. Houliston, Two oppositely localised frizzled RNAs as axis determinants in a cnidarian embryo, PLoS biology, vol.5, issue.4, p.292, 2007.
URL : https://hal.archives-ouvertes.fr/hal-02388291

T. Momose and V. Schmid, Animal pole determinants define oral-aboral axis polarity and endodermal cell-fate in hydrozoan jellyfish Podocoryne carnea, Developmental Biology, vol.292, issue.2, p.173, 2006.

T. Momose, R. Derelle, and E. Houliston, A maternally localised Wnt ligand required for axial patterning in the cnidarian Clytia hemisphaerica, Development, vol.171, issue.12, p.280, 2008.
URL : https://hal.archives-ouvertes.fr/hal-02115404

T. Momose, Y. Kraus, and E. Houliston, A conserved function for Strabismus in establishing planar cell polarity in the ciliated ectoderm during cnidarian larval development, Development, vol.4382, p.176, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02115399

C. M. Moran, R. J. Garriock, M. K. Miller, R. L. Heimark, C. C. Gregorio et al., Expression of the fast twitch troponin complex, fTnT, fTnl and fTnC, in vascular smooth muscle, Cell Motility and the Cytoskeleton, vol.65, issue.8, pp.652-661, 2008.

T. H. Morgan, Regeneration in the Hydromedusa, Gonionemus vertens, vol.33, pp.939-951, 1899.

L. L. Moroz, The ctenophore genome and the evolutionary origins of neural systems, Nature, vol.510, issue.7503, pp.109-114, 2014.

H. A. Müller, R. Samanta, and E. Wieschaus, Wingless signaling in the Drosophila embryo : zygotic requirements and the role of the frizzled genes, vol.126, pp.577-586, 1999.

P. Müller, N. Yanze, V. Schmid, and J. Spring, The Homeobox Gene Otx of the Jellyfish Podocoryne carnea : Role of a Head Gene in Striated Muscle and Evolution, Developmental Biology, vol.216, issue.2, p.156, 1999.

W. Müller, U. Frank, R. Teo, O. Mokady, C. Guette et al., Wnt signaling in hydroid development : Ectopic heads and giant buds induced by GSK-3? inhibitors, International Journal of Developmental Biology, vol.51, issue.3, p.292, 2007.

M. J. Murray, Systems of mutually-triggering event generators : Basic properties and functions in information transmission and rhythm generation, Journal of Comparative Physiology, vol.117, issue.1, pp.63-98, 1977.

S. Nakagawa, S. Takada, R. Takada, and M. Takeichi, Identification of the laminarinducing factor : Wnt-signal from the anterior rim induces correct laminar formation of the neural retina in vitro, Developmental Biology, vol.260, issue.2, pp.414-425, 2003.

N. Nakanishi, D. Yuan, D. K. Jacobs, and V. Hartenstein, Development Genes and Evolution, Early development, pattern, and reorganization of the planula nervous system in Aurelia (Cnidaria, Scyphozoa), vol.218, p.20, 2008.

N. Nakanishi, V. Hartenstein, and D. K. Jacobs, Development of the rhopalial nervous system in Aurelia sp.1 (Cnidaria, Scyphozoa), Development genes and evolution, vol.219, p.287, 2009.

N. Nakanishi, D. Yuan, V. Hartenstein, and D. K. Jacobs, Evolutionary origin of rhopalia : Insights from cellular-level analyses of Otx and POU expression patterns in the developing rhopalial nervous system, Evolution and Development, vol.12, issue.4, pp.404-415, 2010.

, Chapitre 5

A. M. Nawrocki and P. Cartwright, Expression of Wnt pathway genes in polyps and medusa-like structures of Ectopleura larynx (Cnidaria : Hydrozoa), Evolution and Development, vol.15, p.294, 2013.

A. M. Nawrocki, A. G. Collins, Y. M. Hirano, P. Schuchert, and P. Cartwright, Phylogenetic placement of Hydra and relationships within Aplanulata (Cnidaria : Hydrozoa), vol.67, pp.60-71, 2013.

R. Neumann, Polyp morphogenesis in a scyphozoan : Evidence for a head inhibitor from the presumptive foot end in vegetative buds of Cassiopeia andromeda, Wilhelm Roux's Archives of Developmental Biology, vol.183, issue.1, pp.79-83, 1977.

V. Nguyen, K. Deschet, T. Henrich, E. Godet, J. S. Joly et al., Morphogenesis of the optic tectum in the medaka (Oryzias latipes) : A morphological and molecular study, with special emphasis on cell proliferation, Journal of Comparative Neurology, vol.413, issue.3, pp.385-404, 1999.
URL : https://hal.archives-ouvertes.fr/hal-00123336

S. A. Nichols, B. W. Roberts, D. J. Richter, S. R. Fairclough, and N. King, Origin of metazoan cadherin diversity and the antiquity of the classical cadherin/?-catenin complex, Proceedings of the National Academy of Sciences, vol.109, issue.32, p.51, 2012.

C. Niehrs, On growth and form : a Cartesian coordinate system of Wnt and BMP signaling specifies bilaterian body axes, Development, issue.6, pp.845-57, 2010.

C. Nielsen, Animal evolution : interrelationships of the living phyla, p.116, 2012.

A. Niida, T. Hiroko, M. Kasai, Y. Furukawa, Y. Nakamura et al., Dkk1, a negative regulator of Wnt signaling, is a target of the ?catenin/TCF pathway, Oncogene, vol.23, issue.52, pp.8520-8526, 2004.

J. L. Norenburg, Systematic implications of Euphysa ruthae n. sp. (Athecata : Corymorphidae), a psammophilic solitary hydroid with unusual morphogenesis, Transactions, 1983.

, American Microscopical Society, vol.102, issue.1, pp.1-17

T. Nüchter and M. Benoit, Nanosecond-scale kinetics of nematocyst discharge, Cell, vol.16, issue.9, pp.316-318, 2006.

D. M. Odorico and D. J. Miller, Internal and external relationships of the Cnidaria : implications of primary and predicted secondary structure of the 5 '-end of the 23S-like rDNA, Proceedings : Biological Sciences, vol.264, pp.77-82, 1378.

Y. Ohinata, H. Ohta, M. Shigeta, K. Yamanaka, T. Wakayama et al., A Signaling Principle for the Specification of the Germ Cell Lineage in Mice, Cell, vol.137, issue.3, pp.571-584, 2009.

D. Oliver, M. Brinkmann, T. Sieger, and U. Thurm, Hydrozoan nematocytes send and receive synaptic signals induced by mechano-chemical stimuli, Journal of Experimental Biology, vol.211, issue.17, pp.2876-2888, 2008.

T. Onai, A. Takai, D. H. Setiamarga, and L. Z. Holland, Essential role of Dkk3 for head formation by inhibiting Wnt/?-catenin and Nodal/Vg1 signaling pathways in the basal chordate amphioxus, Evolution and Development, vol.14, issue.4, p.311, 2012.

T. Onai, T. Aramaki, H. Inomata, T. Hirai, and S. Kuratani, On the origin of vertebrate somites, Zoological Letters, vol.1, issue.1, p.33, 2015.

S. Özbek, U. Engel, and J. Engel, A switch in disulfide linkage during minicollagen assembly in Hydra nematocysts or how to assemble a 150-bar-resistant structure, Journal of Structural Biology, vol.137, issue.1-2, pp.11-14, 2002.

S. Özbek, P. G. Balasubramanian, and T. W. Holstein, Cnidocyst structure and the biomechanics of discharge, vol.54, pp.1038-1045, 2009.

K. Pang, J. F. Ryan, J. C. Mullikin, A. D. Baxevanis, and M. Q. Martindale, Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi, EvoDevo, vol.1, issue.1, p.278, 2010.

E. Papathanassiou, P. Panayotidis, and K. Anagnostaki, Notes on the Biology and Ecology of the Jellyfish Aurelia aurita Lam. in Elefsis Bay, vol.8, pp.49-58, 1987.

E. Park, D. S. Hwang, J. S. Lee, J. I. Song, T. K. Seo et al., Estimation of divergence times in cnidarian evolution based on mitochondrial protein-coding genes and the fossil record, Molecular Phylogenetics and Evolution, vol.62, p.89, 2012.

L. M. Passano, Pacemakers and activity patterns in medusae : Homage to Romanes, Integrative and Comparative Biology, vol.5, issue.3, p.44, 1965.

L. M. Passano, Behavioral control systems in medusae : A comparison between hydroand scyphomedusae, Publications of the Seto Marine Biological Laboratory, vol.20, p.105, 1973.

L. M. Passano, Scyphozoa and Cubozoa, in Electrical conduction and behaviour in "simple" invertebrates, vol.32, p.44, 1982.

J. C. Pearson, D. Lemons, and W. Mcginnis, Modulating Hox gene functions during animal body patterning, Nature Reviews Genetics, vol.6, issue.12, pp.893-904, 2005.

J. A. Pechenik, Biology of the invertebrates, vol.606, 2010.

E. Percival, On the Strobilization of Aurelia, The Quarterly Journal of Microscopical Science, vol.67, issue.265, p.135, 1923.

J. M. Pérez-pomares and R. Muñoz-chápuli, Epithelial-mesenchymal transitions : A mesodermal cell strategy for evolutive innovation in metazoans, Anatomical Record, vol.268, issue.3, pp.343-351, 2002.

F. Péron and C. A. Lesueur, Tableau des caractères génériques et spécifiques de toutes les espèces de méduses connues jusqu'à ce jour, vol.14, pp.325-366, 1810.

M. Perron, S. Kanekar, M. L. Vetter, and W. A. Harris, The genetic sequence of retinal development in the ciliary margin of the Xenopus eye, Developmental Biology, vol.199, issue.2, pp.185-200, 1998.
URL : https://hal.archives-ouvertes.fr/hal-00740507

C. P. Petersen and P. W. Reddien, Wnt signaling and the polarity of the primary body axis, Cell, issue.6, p.170, 2009.

H. O. Petersen, A comprehensive transcriptomic and proteomic analysis of Hydra head regeneration, Molecular Biology and Evolution, vol.32, issue.8, pp.1928-1947, 2015.

K. W. Petersen, Development of coloniality in Hydrozoa, Biology and Systematics of Colonial Organisms, vol.71, p.74, 1979.

K. W. Petersen, Evolution and taxonomy in capitate hydroids and medusae (Cnidaria : Hydrozoa), Zoological Journal of the Linnean Society, vol.100, issue.2, p.393, 1990.

K. J. Peterson and E. A. Sperling, Poriferan ANTP genes : Primitively simple or secondarily reduced ?, Evolution and Development, vol.9, issue.5, pp.405-408, 2007.

I. Philipp, T. W. Holstein, and B. Hobmayer, HvJNK, a Hydra member of the c-Jun NH2-terminal kinase gene family, is expressed during nematocyte differentiation, Gene Expression Patterns, vol.5, issue.3, pp.397-402, 2005.

I. Philipp, R. Aufschnaiter, S. Ozbek, S. Pontasch, M. Jenewein et al., Wnt/?-catenin and noncanonical Wnt signaling interact in tissue evagination in the simple eumetazoan Hydra, Proceedings of the National Academy of Sciences of the United States of America, vol.106, p.294, 2009.

H. Philippe, Phylogenomics revives traditional views on deep animal relationships, vol.19, pp.706-718, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00594690

S. Piraino, G. Zega, C. D. Benedetto, A. Leone, A. Dell'anna et al., Complex neural architecture in the diploblastic larva of Clava multicornis (Hydrozoa, Cnidaria), Journal of Comparative Neurology, vol.519, issue.10, pp.1931-1951, 2011.

D. C. Plachetzki, C. R. Fong, and T. H. Oakley, Cnidocyte discharge is regulated by light and opsin-mediated phototransduction, BMC Biology, vol.10, issue.1, p.17, 2012.

G. Plickert, V. Jacoby, U. Frank, W. A. Müller, and O. Mokady, Wnt signaling in hydroid development : Formation of the primary body axis in embryogenesis and its subsequent patterning, Developmental Biology, vol.298, issue.2, p.173, 2006.

D. Ponce, D. L. Brinkman, J. Potriquet, and J. Mulvenna, Tentacle transcriptome and venom proteome of the pacific sea nettle, Chrysaora fuscescens (Cnidaria : Scyphozoa), vol.8, p.102, 2016.

M. Pratlong, C. Rancurel, P. Pontarotti, and D. Aurelle, Cnidaria) : why do nuclear and mitochondrial phylogenies disagree ?, Monophyly of Anthozoa, vol.46, pp.363-371, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01474009

J. E. Purcell, Aggressive Function and Induced Development of Catch Tentacles in the Sea Anemone Metridium senile (Coelenterata, Actiniaria), Biological Bulletin, vol.153, issue.2, pp.355-368, 1977.

N. H. Putnam, Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization, Science, issue.5834, pp.86-94, 2007.

T. M. Puvirajesinghe, Identification of p62/SQSTM1 as a component of noncanonical Wnt VANGL2-JNK signalling in breast cancer, Nature Communications, vol.7, issue.10, p.318, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01447570

G. Quiroga-artigas, P. Lapébie, L. Leclère, N. Takeda, R. Deguchi et al., A gonad-expressed opsin mediates light-induced spawning in the jellyfish Clytia, eLife, 7, e29, vol.47, p.116, 2018.

. R-core-team, R : A Language and Environment for Statistical Computing, p.254, 2017.

P. M. Ralph, New Zealand Thecate Hydroids. Part V. The Distribution of the New Zealand Thecate Hydroids, vol.1, pp.103-111, 1961.

P. Raven, G. Johnson, K. Mason, J. Losos, and S. Singer, Biology, p.68, 2017.

S. Reber-müller, R. Streitwolf-engel, N. Yanze, V. Schmid, M. Stierwald et al., BMP2/4 and BMP5-8 in jellyfish development and transdifferentiation, International Journal of Developmental Biology, vol.50, issue.4, p.390, 2006.

P. C. Reddy, M. K. Unni, A. Gungi, P. Agarwal, and S. Galande, Evolution of Hox-like genes in Cnidaria : Study of Hydra Hox repertoire reveals tailor-made Hox-code for Cnidarians, Mechanisms of Development, vol.138, pp.87-96, 2015.

, Chapitre 5

B. Reinhardt, M. Broun, I. L. Blitz, and H. R. Bode, HyBMP5-8b, a BMP5-8 orthologue, acts during axial patterning and tentacle formation in Hydra, Developmental Biology, vol.267, issue.1, p.162, 2004.

A. M. Reitzel, L. Behrendt, and A. M. Tarrant, Light entrained rhythmic gene expression in the sea anemone Nematostella vectensis : The evolution of the animal circadian clock, PLoS ONE, vol.5, issue.9, pp.1-9, 2010.

S. Rennoll and G. Yochum, Regulation of MYC gene expression by aberrant Wnt/?catenin signaling in colorectal cancer, World Journal of Biological Chemistry, vol.6, issue.4, pp.290-300, 2015.

F. Rentzsch, C. Guder, D. Vocke, B. Hobmayer, and T. W. Holstein, An ancient chordinlike gene in organizer formation of Hydra, Proceedings of the National Academy of Sciences, vol.104, issue.9, p.162, 2007.

F. Rentzsch, J. H. Fritzenwanker, C. B. Scholz, and U. Technau, FGF signalling controls formation of the apical sensory organ in the cnidarian Nematostella vectensis, Development, vol.135, issue.10, pp.1761-1769, 2008.

F. Rentzsch, M. Layden, and M. Manuel, The cellular and molecular basis of cnidarian neurogenesis, Wiley Interdisciplinary Reviews : Developmental Biology, vol.6, issue.1, p.257, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01405097

B. Reversade and E. M. De-robertis, Regulation of ADMP and BMP2/4/7 at opposite embryonic poles generates a self-regulating morphogenetic field, Cell, vol.123, issue.6, pp.1147-1160, 2005.

R. H. Richmond, Energetics, competency, and long-distance dispersal of planula larvae of the coral Pocillopora damicornis, Marine Biology, vol.93, issue.4, pp.527-533, 1987.

R. M. Rieger and P. Ladurner, The significance of muscle cells for the origin of mesoderm in bilateria, Integrative and comparative biology, vol.43, issue.1, pp.47-54, 2003.

A. Riesgo, N. Farrar, P. J. Windsor, G. Giribet, and S. P. Leys, The analysis of eight transcriptomes from all poriferan classes reveals surprising genetic complexity in sponges, Molecular Biology and Evolution, vol.31, issue.5, pp.1102-1120, 2014.

T. Rigo-watermeier, B. Kraft, M. Ritthaler, V. Wallkamm, T. Holstein et al., Functional conservation of Nematostella Wnts in canonical and noncanonical Wnt-signaling, Biology Open, vol.1, issue.1, p.389, 2012.

C. S. Rodriguez, A. C. Marques, S. N. Stampar, A. C. Morandini, E. Christiansen et al.,

H. W. Genzano and . Mianzan, The taxonomic position of the pelagic 'staurozoan' Tessera gemmaria as a ceriantharian larva, Zootaxa, vol.75, pp.49-58, 2011.

G. J. Romanes, Jelly-fish, star-fish, and sea-urchins, being a research on primitive nervous systems, The International scientific series, vol.1, p.282, 1885.

E. Röttinger, P. Dahlin, and M. Q. Martindale, A Framework for the Establishment of a Cnidarian Gene Regulatory Network for "Endomesoderm" Specification : The Inputs of ßcatenin/TCF Signaling, PLoS Genetics, vol.8, issue.12, p.246, 1003.

A. Ruggiero, Impact of Wnt signalling on multipotent stem cell dynamics during Clytia hemisphaerica embryonic and larval development, vol.177, p.244, 2015.
URL : https://hal.archives-ouvertes.fr/tel-01490272

B. Runnegar, Precambrian oxygen levels estimated from the biochemistry and physiology of early eukaryotes, Global and Planetary Change, vol.5, issue.1-2, pp.97-111, 1991.

F. Russell, Limnomedusae, Trachymedusae and Narcomedusae, 530 pp, vol.I -Hydrozoa. Anthomedusae, Leptomedusae, p.118, 1953.

F. Russell, II -Pelagic Scyphozoa, with a supplement to, vol.I, p.385, 1970.

J. F. Ryan, The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution, Science, vol.342, issue.6164, p.252, 2013.

M. Saina, G. Genikhovich, E. Renfer, U. Technau, and J. C. Gerhart, BMPs and Chordin regulate patterning of the directive axis in a sea anemone, Proceedings of the National Academy of Sciences, vol.106, issue.44, pp.592-610, 2009.

S. M. Sanders and P. Cartwright, Interspecific Differential Expression Analysis of RNA-Seq Data Yields Insight into Life Cycle Variation in Hydractiniid Hydrozoans, Genome biology and evolution, vol.7, issue.8, pp.2417-2448, 2015.

S. M. Sanders and P. Cartwright, Patterns of Wnt signaling in the life cycle of Podocoryna carnea and its implications for medusae evolution in Hydrozoa (Cnidaria), Evolution and Development, vol.17, p.308, 2015.

S. M. Sanders, M. Shcheglovitova, and P. Cartwright, Differential gene expression between functionally specialized polyps of the colonial hydrozoan Hydractinia symbiolongicarpus (Phylum Cnidaria), BMC genomics, vol.15, issue.1, p.406, 2014.

T. Saneyoshi, S. Kume, Y. Amsaki, and K. Mikoshiba, The Wnt/calcium pathway activates NF-AT and promotes ventral cell fate in Xenopus embryos, Nature, issue.6886, pp.295-299, 2002.

A. D. Sappenfield, L. G. Tarhan, and M. L. Droser, Earth's oldest jellyfish strandings : A unique taphonomic window or just another day at the beach ?, Geological Magazine, vol.154, issue.4, p.88, 2017.

M. P. Sarras, M. E. Madden, X. Zhang, S. Gunwar, J. K. Huff et al., Extracellular matrix (mesoglea) of Hydra vulgaris. I. Isolation and characterization, Developmental, Biology, vol.148, issue.2, pp.481-494, 1991.

M. Sars, Bidrag til Söedyrenes Naturhistorie, 1829.

M. Sars, Über die Entwicklung der Medusa Aurelia aurita und der Cyanea capillata, Archiv für Naturgeschichte, vol.7, issue.4, pp.9-34, 1841.

A. Sato, T. Kojima, K. Ui-tei, Y. Miyata, and K. Saigo, Dfrizzled-3, a new Drosophila Wnt receptor, acting as an attenuator of Wingless signaling in wingless hypomorphic mutants, Development, issue.20, pp.4421-4451, 1999.

R. A. Satterlie, Central generation of swimming activity in the hydrozoan jellyfish Aequorea aequorea, Journal of Neurobiology, vol.16, issue.1, pp.41-55, 1985.

R. A. Satterlie, Neuronal control of swimming in jellyfish : a comparative story, Canadian Journal of Zoology, vol.80, issue.10, p.45, 2002.

R. A. Satterlie, Do jellyfish have central nervous systems ?, Journal of Experimental Biology, vol.214, issue.8, pp.1215-1223, 2011.

R. A. Satterlie and J. M. Eichinger, Organization of the Ectodermal Nervous Structures in Jellyfish : Scyphomedusae, The Biological Bulletin, vol.226, p.106, 2014.

R. A. Satterlie and A. N. Spencer, Neuronal control of locomotion in hydrozoan medusae, Journal of Comparative Physiology, vol.150, issue.2, pp.195-206, 1983.

R. A. Satterlie, K. S. Thomas, and G. C. Gray, Muscle organization of the cubozoan jellyfish Tripedalia cystophora Conant 1897, Biological Bulletin, vol.209, issue.2, p.385, 2005.

E. A. Schafer, Observations on the Nervous System of Aurelia Aurita, vol.169, p.50, 1878.

A. A. Schaffer, M. Bazarsky, K. Levy, V. Chalifa-caspi, and U. Gat, A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis, BMC Genomics, vol.17, issue.1, p.281, 2016.

Q. Schenkelaars, L. Fierro-constain, E. Renard, A. L. Hill, and C. Borchiellini, Insights into Frizzled evolution and new perspectives, Evolution and Development, vol.17, issue.2, p.256, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01444864

G. Schmahl, Bacterially induced stolon settlement in the scyphopolyp of Aurelia aurita (Cnidaria, Scyphozoa), Helgoländer Meeresuntersuchungen, vol.39, pp.33-42, 1985.

J. Schmich, Y. Kraus, D. Vito, D. Graziussi, F. Boero et al., Induction of reverse development in two marine Hydrozoans, International Journal of Developmental Biology, vol.51, issue.1, p.60, 2007.

B. Schmid, V. Schmid, and P. Tardent, The umbrellar growth process in the leptomedusae Phialidium hemisphaericum (Syn. Campanularia johnstoni), Experientia, issue.12, pp.1399-1400, 1974.

V. Schmid, Untersuchungen über Dedifferenzierungsvorgänge bei Medusenknospen und Medusen von Podocoryne carnea M. Sars, Wilhelm Roux' Archiv, vol.307, pp.281-307, 1972.

V. Schmid, Regeneration in medusa buds and medusae of hydrozoa, Integrative and Comparative Biology, vol.14, issue.2, pp.773-781, 1974.

V. Schmid, Transdifferentiation in Medusae, International Review of Cytology, vol.57, issue.142, p.388, 1992.

V. Schmid and S. Reber-müller, Transdifferentiation of isolated striated muscle of jellyfish in vitro : The initiation process, Seminars in Cell and Developmental Biology, vol.6, issue.3, pp.109-116, 1995.

V. Schmid and P. Tardent, The reconstitutional performances of the Leptomedusa Campanularia jonstoni, Marine Biology, vol.8, issue.2, p.63, 1971.

V. Schmid, B. Schmid, B. Schneider, R. Stidwill, and G. Baker, Factors effecting manubrium-regeneration in hydromedusae (Coelenterata), Wilhelm Roux's Archives of Developmental, Biology, vol.179, issue.1, p.387, 1976.

V. Schmid, H. Alder, G. Plickert, and C. Weber, Transdifferentiation from striated muscle of medusae in vitro, Cell Differentiation and Development, vol.25, pp.137-146, 1988.

G. Scholtz, Deconstructing morphology, Acta Zoologica, vol.91, issue.1, pp.44-63, 2010.

P. Schuchert, Phylogenetic analysis of the Cnidaria, Journal of Zoological Systematics and Evolutionary Research, vol.31, issue.3, pp.161-173, 2009.

P. Schuchert, S. Reber-müller, and V. Schmid, Life stage specific expression of a myosin heavy chain in the hydrozoan Podocoryne carnea, Differentiation, vol.54, issue.1, p.124, 1993.

S. Scorrano, G. Aglieri, F. Boero, M. N. Dawson, and S. Piraino, Unmasking Aurelia species in the Mediterranean Sea : An integrative morphometric and molecular approach, Zoological Journal of the Linnean Society, vol.180, issue.2, pp.243-267, 2017.

J. R. Seifert and M. Mlodzik, Frizzled/PCP signalling : A conserved mechanism regulating cell polarity and directed motility, Nature Reviews Genetics, vol.8, issue.2, pp.126-138, 2007.

, Chapitre 5

M. Seimiya, H. Ishiguro, K. Miura, Y. Watanabe, and Y. Kurosawa, Homeoboxcontaining genes in the most primitive metazoa, the sponges, European Journal of Biochemistry, vol.221, issue.1, pp.219-225, 1994.

K. Seipel and V. Schmid, Evolution of striated muscle : Jellyfish and the origin of triploblasty, Developmental Biology, vol.282, issue.1, p.153, 2005.

K. Seipel and V. Schmid, Mesodermal anatomies in cnidarian polyps and medusae, International Journal of Developmental Biology, vol.50, issue.7, p.150, 2006.

K. Seipel, N. Yanze, and V. Schmid, Developmental and evolutionary aspects of the basic helix-loop-helix transcription factors Atonal-like 1 and Achaete-scute homolog 2 in the jellyfish, Developmental Biology, vol.269, p.151, 2004.

K. Seipel, N. Yanze, and V. Schmid, The germ line and somatic stem cell gene Cniwi in the jellyfish Podocoryne carnea, International Journal of Developmental Biology, vol.48, issue.1, pp.1-7, 2004.

T. Shaposhnikova, I. Matveev, T. Napara, and O. Podgornaya, Mesogleal cells of the jellyfish Aurelia aurita are involved in the formation of mesogleal fibres, Cell Biology International, vol.29, issue.11, pp.952-958, 2005.

C. Shinzato, M. Inoue, and M. Kusakabe, A snapshot of a coral "holobiont" : A transcriptome assembly of the scleractinian coral, Porites, captures a wide variety of genes from both the host and symbiotic zooxanthellae, PLoS ONE, vol.9, issue.1, p.182, 2014.

C. Shinzato, Using the Acropora digitifera genome to understand coral responses to environmental change, Nature, vol.476, issue.7360, pp.320-323, 2011.

F. Sievers, Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega, Molecular Systems Biology, vol.7, issue.1, 2011.

P. Simion, A Large and Consistent Phylogenomic Dataset Supports Sponges as the Sister Group to All Other Animals, Current Biology, vol.27, issue.7, p.376, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01681528

C. L. Singla, Ocelli of hydromedusae, Cell and Tissue Research, vol.149, issue.3, pp.413-429, 1974.

C. L. Singla, Statocysts of hydromedusae, Cell and Tissue Research, vol.158, issue.3, p.107, 1975.

C. L. Singla, Fine structure of the sensory receptors of Aglantha digitale (Hydromedusae : Trachylina), vol.231, pp.415-425, 1983.

C. Sinigaglia, H. Busengdal, L. Leclère, U. Technau, and F. Rentzsch, The Bilaterian Head Patterning Gene six3/6 Controls Aboral Domain Development in a Cnidarian, PLoS Biology, vol.11, issue.2, p.171, 2013.

C. Sinigaglia, D. Thiel, A. Hejnol, E. Houliston, and L. Leclère, A safer, urea-based in situ hybridization method improves detection of gene expression in diverse animal species, Developmental Biology, vol.434, issue.1, pp.15-23, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01655963

D. B. Slautterback and D. W. Fawcett, The Development of the Cnidoblasts of Hydra : An Electron Microscope Study of Cell Differentiation, The Journal of Cell Biology, vol.5, issue.3, pp.441-452, 1959.

K. M. Smith, L. Gee, I. L. Blitz, and H. R. Bode, CnOtx, a member of the Otx gene family, has a role in cell movement in hydra, Developmental biology, vol.212, issue.2, pp.392-404, 1999.

S. Y. Sokol, Maintaining embryonic stem cell pluripotency with Wnt signaling, Development, vol.138, pp.4341-4350, 2011.

C. Sommer, Larval biology and dispersal of Eudendrium racemosum (Hydrozoa, Eudendriidae), vol.56, pp.205-211, 1992.

I. Sötje and G. Jarms, Derivation of the reduced life cycle of Thecoscyphus zibrowii Werner, Cnidaria, Scyphozoa), vol.156, p.139, 1984.

D. B. Spangenberg, A study of strobilation in Aurelia aurita under controlled conditions, Journal of Experimental Zoology, vol.160, issue.1, p.256, 1965.

D. B. Spangenberg, Iodine induction of metamorphosis in Aurelia, Journal of Experimental Zoology, vol.165, issue.3, pp.441-449, 1967.

D. B. Spangenberg, Statolith differentiation in Aurelia aurita, Journal of Experimental Zoology, vol.169, issue.4, pp.487-499, 1968.

D. B. Spangenberg, Recent studies of strobilation in jellyfish, Oceanographic Marine Biological Annual Review, vol.6, pp.231-247, 1968.

A. N. Spencer and W. E. Schwab, Hydrozoa, in Electrical Conduction and Behaviour in "Simple" Invertebrates, vol.104, pp.73-148, 1982.

R. C. Sprigg, Early Cambrian ( ?) Jellyfishes from the Flinders Ranges, vol.71, p.86, 1947.

J. Spring, N. Yanze, A. M. Middel, M. Stierwald, H. Gröger et al., The Mesoderm Specification Factor Twist in the Life Cycle of Jellyfish, Developmental Biology, vol.228, issue.2, p.151, 2000.

J. Spring, N. Yanze, C. Jösch, A. M. Middel, B. Winninger et al., Conservation of Brachyury, Mef2, and Snail in the myogenic lineage of jellyfish : a connection to the 433, 2002.

, Chapitre 5 mesoderm of Bilateria, Developmental Biology, vol.244, issue.2, p.151

M. Srivastava, The Trichoplax genome and the nature of placozoans, Nature, vol.179, issue.7207, p.254, 2008.

M. Srivastava, The Amphimedon queenslandica genome and the evolution of animal complexity, Nature, vol.466, issue.7307, pp.720-726, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00519655

A. Stamatakis, RAxML version 8 : A tool for phylogenetic analysis and post-analysis of large phylogenies, Bioinformatics, vol.30, issue.9, p.307, 2014.

P. R. Steinmetz, Independent evolution of striated muscles in cnidarians and bilaterians, Nature, vol.487, issue.7406, p.391, 2012.
URL : https://hal.archives-ouvertes.fr/hal-02115417

C. R. Stockard, Studies of tissue growth. I. On experimental study of the rate of regeneration in Cassiopea xamachana (Bigelow), 1908.

, , vol.2, pp.61-102

C. R. Stockard, Studies of tissue growth. II. Functional activity, form regulation, level of the cut, and degree of injury as factors in determining the rate of regeneration. The reaction of regenerating tissue on the old body, Journal of Experimental Zoology, Part A : Ecological Genetics and Physiology, vol.6, issue.3, p.62, 1909.

C. R. Stockard, Studies of Tissue Growth. III. The Rates of Regenerative Growth in Different Salt Solutions. IV. The Influence of Regenerating Tissue on the Animal Body, Archiv für Entwicklungsmechanik der Organismen, vol.29, p.61, 1909.

D. R. Stokes, Physiological studies of conducting systems in the colonial hydroid Hydractinia echinata. I. Polyp specialization, Journal of Experimental Zoology, vol.190, issue.1, pp.1-17, 1974.

I. Straehler-pohl and G. Jarms, Life cycle of Carybdea marsupialis Linnaeus, 1758 (Cubozoa, Carybdeidae) reveals metamorphosis to be a modified strobilation, Marine Biology, vol.147, issue.6, p.392, 2005.

I. Straehler-pohl, C. L. Widmer, and A. C. Morandini, Characterizations of juvenile stages of some semaeostome Scyphozoa (Cnidaria), with recognition of a new family (Phacellophoridae), vol.37, p.128, 2011.

M. Stumpf, B. Will, K. Wittig, J. Kasper, B. Fischer et al., An organizing region in metamorphosing hydrozoan planula larvae -Stimulation of axis formation in both larval and in adult tissue, International Journal of Developmental Biology, vol.54, issue.5, p.249, 2010.

K. Sukhdeo, M. Mani, T. Hideshima, K. Takada, V. Pena-cruz et al.,

D. R. Anderson and . Carrasco, ?-catenin is dynamically stored and cleared in multiple myeloma by the proteasome-aggresome-autophagosome-lysosome pathway, Leukemia, vol.26, issue.5, pp.1116-1119, 2012.

S. Szczepanek, M. Cikala, and C. N. David, Poly-gamma-glutamate synthesis during formation of nematocyst capsules in Hydra, Journal of cell science, vol.115, issue.4, pp.745-51, 2002.

C. Taddei-ferretti and C. Musio, Photobehaviour of Hydra (Cnidaria, Hydrozoa) and correlated mechanisms : A case of extraocular photosensitivity, Journal of Photochemistry and Photobiology B : Biology, vol.55, issue.2-3, pp.88-101, 2000.

T. Takahashi and N. Takeda, Insight into the molecular and functional diversity of cnidarian neuropeptides, International Journal of Molecular Sciences, vol.16, issue.2, pp.2610-2625, 2015.

Y. Takaku, J. S. Hwang, A. Wolf, A. Böttger, H. Shimizu et al., Innexin gap junctions in nerve cells coordinate spontaneous contractile behavior in Hydra polyps, Scientific Reports, vol.4, issue.1, p.3573, 2014.

P. Tardent, A-I ; 71-415, Coelenterata, Cnidaria, in Morphogenese der Tiere, vol.136, p.150, 1978.

P. Tardent, The Differentiation of Germ Cells in Cnidaria, in The origin and evolution of sex, p.116, 1985.

U. Technau and C. B. Scholz, Origin and evolution of endoderm and mesoderm, The International journal of developmental biology, vol.47, issue.7-8, pp.531-539, 2003.

U. Technau and R. E. Steele, Evolutionary crossroads in developmental biology : Cnidaria, vol.158, p.165, 2011.

U. Technau, G. Genikhovich, and J. E. Kraus, Cnidaria, in Evolutionary Developmental Biology of Invertebrates, vol.1, p.38, 2015.

R. M. Teo, The Wnt Cascade and Stem Cell Fate in a Basic Metazoan, vol.177, p.244, 2005.

H. Thiel, Untersuchungen über die Strobilisation von Aurelia aurita Lam. an einer Population der Kieler Förde, Kieler Meeresforsch, vol.13, 1962.

H. Thiel, Untersuchungen über die Entstehung abnormer Scyphistomae, Strobilae und Ephyrae von Aurelia aurita Lam. und ihre theoretische Bedeutung, Zoologische Jahrbücher : Abteilung für Anatomie und Ontogenie der Tiere, vol.81, pp.311-358, 1963.

H. Thiel, The Evolution of Scyphozoa : A review, Cnidaria and their Evolution, p.287, 1966.

M. B. Thomas, G. Freeman, and V. J. Martin, The Embryonic Origin of Neurosensory Cells and the Role of Nerve Cells in Metamorphosis in Phialidium gregarium (Cnidaria, Hydrozoa), International Journal of Invertebrate Reproduction and Development, vol.11, issue.3, p.9, 1987.

M. Thomas-chollier, V. Ledent, L. Leyns, and M. Vervoort, A non-tree-based comprehensive study of metazoan Hox and ParaHox genes prompts new insights into their origin and evolution, BMC evolutionary biology, vol.10, issue.1, p.73, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00486240

C. Thrasivoulou, M. Millar, and A. Ahmed, Activation of intracellular calcium by multiple Wnt ligands and translocation of ?-catenin into the nucleus : A convergent model of, 2013.

, Wnt/Ca2+ and Wnt/?-catenin pathways, Journal of Biological Chemistry, vol.288, issue.50, pp.651-686

U. Thurm, M. Brinkmann, R. Golz, M. Holtmann, D. Oliver et al., Mechanoreception and synaptic transmission of hydrozoan nematocytes, Hydrobiologia, issue.1-3, p.185, 2004.

X. Tian, Z. Liu, B. Niu, J. Zhang, T. K. Tan et al., E-Cadherin/?-catenin complex and the epithelial barrier, Journal of Biomedicine and Biotechnology, vol.567, p.305, 2011.

H. Tiemann and G. Jarms, Organ-like gonads, complex oocyte formation, and long-term spawning in Periphylla periphylla (Cnidaria, Scyphozoa, Coronatae), Marine Biology, vol.157, issue.3, pp.527-535, 2010.

M. A. Torres, J. A. Yang-snyder, S. M. Purcell, A. A. Demarais, L. L. Mcgrew et al., Activities of the Wnt-1 class of secreted signaling factors are antagonized by the Wnt-5A class and by a dominant negative cadherin in early Xenopus development, Journal of Cell Biology, vol.133, issue.5, pp.1123-1137, 1996.

S. Toshino, H. Miyake, S. Ohtsuka, K. Okuizumi, A. Adachi et al., Development and polyp formation of the giant box jellyfish Morbakka virulenta (Kishinouye, 1910) (Cnidaria : Cubozoa) collected from the Seto Inland Sea, western Japan, Plankton and Benthos Research, vol.8, issue.1, p.133, 2013.

S. Toshino, H. Miyake, and S. Iwanaga, Development of Copula sivickisi (Stiasny, 1926) (Cnidaria : Cubozoa : Carybdeidae : Tripedaliidae) collected from the Ryukyu Archipelago, southern Japan, Plankton and Benthos Research, vol.9, pp.32-41, 2014.

S. Toshino, H. Miyake, S. Ohtsuka, A. Adachi, Y. Kondo et al., Monodisc strobilation in Japanese giant box jellyfish Morbakka virulenta (Kishinouye, 1910) : a strong implication of phylogenetic similarity between Cubozoa and Scyphozoa, Evolution and Development, vol.17, issue.4, p.392, 2015.

S. Toshino, H. Miyake, and H. Shibata, Meteorona kishinouyei, a new family, genus and species (Cnidaria, Cubozoa, Chirodropida) from Japanese waters, ZooKeys, vol.102, issue.503, p.123, 2015.

K. M. Towe, Oxygen-Collagen Priority and the Early Metazoan Fossil Record, Proceedings of the National Academy of Sciences, vol.65, pp.781-788, 1970.

M. Trevino, D. J. Stefanik, R. Rodriguez, S. Harmon, and P. M. Burton, Induction of canonical Wnt signaling by alsterpaullone is sufficient for oral tissue fate during regeneration 436 and embryogenesis in Nematostella vectensis, Developmental dynamics : an official publication of the, vol.240, p.172, 2011.

T. Uchida and Z. Nagao, The metamorphosis of the scyphomedusae, Aurelia limbata (Brandt), Annotationes Zoologicae Japonenses, vol.36, issue.2, p.54, 1963.

A. Vagelli, New observations on the asexual reproduction of Aurelia aurita (Cnidaria, Scyphozoa) with comments on its life cycle and adaptive significance, Invertebrate zoology, vol.4, issue.2, pp.111-127, 2007.

R. Van-amerongen, C. Fuerer, M. Mizutani, and R. Nusse, Wnt5a can both activate and repress Wnt/?-catenin signaling during mouse embryonic development, Developmental Biology, vol.369, issue.1, pp.101-114, 2012.

H. Van-iten, A. C. Marques, J. D. Leme, M. L. Pacheco, and M. G. Simões, Origin and early diversification of the phylum Cnidaria Verrill : Major developments in the analysis of the taxon's proterozoic-cambrian history, Palaeontology, vol.57, issue.4, pp.677-690, 2014.

M. T. Veeman, D. C. Slusarski, A. Kaykas, S. H. Louie, and R. T. Moon, Zebrafish Prickle, a Modulator of Noncanonical Wnt/Fz Signaling, Regulates Gastrulation Movements, Current Biology, vol.13, pp.680-685, 2003.

M. Visweswaran, S. Pohl, F. Arfuso, P. Newsholme, R. Dilley et al., Multi-lineage differentiation of mesenchymal stem cells -To Wnt, or not Wnt, International Journal of Biochemistry and Cell Biology, vol.68, pp.139-147, 2015.

L. Von-salvini-plawen, On the origin and evolution of the lower Metazoa, Journal of Zoological Systematics and Evolutionary Research, vol.16, p.95, 1978.

A. Wallberg, M. Thollesson, J. S. Farris, and U. Jondelius, The phylogenetic position of the comb jellies (Ctenophora) and the importance of taxonomic sampling, Cladistics, vol.20, issue.6, pp.558-578, 2004.

H. Watanabe, A. Kuhn, M. Fushiki, K. Agata, S. Özbek et al., Sequential actions of ?-catenin and Bmp pattern the oral nerve net in Nematostella vectensis, Nature communications, vol.5, p.5536, 2014.

J. Weber, Poly(gamma-glutamic Acid)s Are the Major Constituents of Nematocysts in Hydra (Hydrozoa, Cnidaria), Journal of Biological Chemistry, vol.265, issue.17, pp.9664-9669, 1990.

Y. Wenger, W. Buzgariu, and B. Galliot, Loss of neurogenesis in Hydra leads to compensatory regulation of neurogenic and neurotransmission genes in epithelial cells, Philosophical Transactions of the Royal Society B : Biological Sciences, vol.371, 1685.

B. Werner, Stephanoscyphus (Scyphozoa, Coronatae) und seine direkte Abstammung von den fossilen Conulata, Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.13, issue.4, p.134, 1966.

B. Werner, Stephanoscyphus planulophorus n. spec., ein neuer Scyphopolyp mit einem neuen Entwicklungsmodus, Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.22, issue.1, pp.120-140, 1971.

B. Werner, New investigations on systematics and evolution of the class Scyphozoa and the phylum Cnidaria, vol.20, p.127, 1973.

B. Werner, Stephanoscyphus eumedusoides n. spec. (Scyphozoa, Coronatae), ein Höhlenpolyp mit einem neuen Entwicklungsmodus, Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.26, pp.434-463, 1974.

B. Werner, Bau und Lebensgeschichte des Polypen von Tripedalia cystophora (Cubozoa, class. nov., Carybdeidae) und seine Bedeutung für die Evolution der Cnidaria, Helgoländer Wissenschaftliche Meeresuntersuchungen, vol.27, issue.4, pp.461-504, 1975.

B. Werner, Die Metamorphose des Polypen von Tripedalia cystophora (Cubozoa, Carybdeidae) in die Meduse, Helgoländer Meeresuntersuchungen, vol.36, issue.3, pp.257-276, 1983.

B. Werner, Lehrbuch der Speziellen Zoologie, Band I : Wirbellose Tiere. 2 Teil : Cnidaria, Ctenophora, Mesozoa, Plathelminthes, Nemertini, Entoprocta, Nemathelminthes, Priapulida, vol.74, p.143, 1984.

J. A. Westfall, Ultrastructure of synapses in the first-evolved nervous systems, Journal of neurocytology, vol.25, issue.1, pp.735-746, 1996.

J. A. Westfall, C. F. Elliott, and R. W. Carlin, Ultrastructural evidence for two-cell and three-cell neural pathways in the tentacle epidermis of the sea anemone Aiptasia pallida, Journal of Morphology, issue.1, pp.83-92, 2002.

H. E. Westlake and L. R. Page, Muscle and nerve net organization in stalked jellyfish (Medusozoa : Staurozoa), vol.278, p.385, 2017.

N. V. Whelan, K. M. Kocot, L. L. Moroz, and K. M. Halanych, Error, signal, and the placement of Ctenophora sister to all other animals, Proceedings of the National Academy of Sciences, vol.112, issue.18, pp.5773-5778, 2015.

W. Wietrzykowski, Recherches sur le développement des Lucernaires, Archives de zoologie expérimentale et générale, 5, 1-95, plus Plates I, II, vol.133, p.147, 1912.

. Wikipedia, Wnt signaling pathway, p.237, 2018.

A. H. Wikramanayake, M. Hong, P. N. Lee, K. Pang, C. A. Byrum et al., An ancient role for nuclear ?-catenin in the evolution of axial polarity and germ layer segregation, Nature, vol.426, issue.6965, pp.446-450, 2003.

K. Willert, J. D. Brown, E. Danenberg, A. W. Duncan, I. L. Weissman et al., Wnt proteins are lipid-modified and can act as stem cell growth factors, Nature, vol.423, issue.6938, pp.448-452, 2003.

R. B. Williams, Catch-tentacles in sea anemones : Occurrence in Haliplanella luciae (Verrill) and a review of current knowledge, Journal of Natural History, vol.9, issue.3, pp.241-248, 1975.

T. M. Williams, M. E. Williams, R. Kuick, D. Misek, K. Mcdonagh et al., Candidate downstream regulated genes of Hox group 13 transcription factors with and without monomeric DNA binding capability, Developmental Biology, vol.279, issue.2, pp.462-480, 2005.

J. H. Won, B. J. Rho, and J. I. Song, A phylogenetic study of the Anthozoa (phylum Cnidaria) based on morphological and molecular characters, Coral Reefs, vol.20, issue.1, pp.39-50, 2001.

G. T. Wong, B. J. Gavin, and A. P. Mcmahon, Differential transformation of mammary epithelial cells by Wnt genes, Molecular and Cellular biology, vol.14, issue.9, pp.6278-86, 1994.

R. L. Wood and A. M. Kuda, Formation of junctions in regenerating Hydra : GAP junctions, Journal of Ultrastructure Research, vol.73, issue.3, pp.350-360, 1980.

L. Yamamori, K. Okuizumi, C. Sato, S. Ikeda, and H. Toyohara, Comparison of the Inducing Effect of Indole Compounds on Medusa Formation in Different Classes of Medusozoa, vol.34, p.392, 2017.

T. Yamasu and M. Yoshida, Electron microscopy on the photoreceptors of an anthomedusa and a scyphomedusa, vol.20, pp.757-778, 1973.

N. Yanze, J. Spring, C. Schmidli, and V. Schmid, Conservation of Hox/ParaHox-related genes in the early development of a cnidarian, Developmental biology, vol.236, issue.1, p.385, 2001.

G. A. Young and J. W. Hagadorn, The fossil record of cnidarian medusae, Palaeoworld, vol.19, issue.3-4, p.86, 2010.

D. Yuan, N. Nakanishi, D. K. Jacobs, and V. Hartenstein, Embryonic development and metamorphosis of the scyphozoan Aurelia, Development Genes and Evolution, vol.218, issue.10, p.133, 2008.

C. J. Zagal, Morphological abnormalities in the stauromedusa Haliclystus auricula (Cnidaria) and their possible causes, Journal of the Marine Biological Association of the United Kingdom, vol.88, issue.2, pp.259-262, 2008.

I. S. Zakharov, N. L. Hayes, V. N. Ierusalimsky, R. S. Nowakowski, and P. M. Balaban, Postembryonic neuronogenesis in the procerebrum of the terrestrial snail, Helix lucorum L, vol.35, pp.271-276, 1998.

F. Zapata, Phylogenomic analyses support traditional relationships within Cnidaria, Plos ONE, vol.10, issue.10, p.141, 2015.