D. Gospodarowicz, G. Greenburg, and C. R. Birdwell, Determination of cellular shape by the extracellular matrix and its correlation with the control of cellular growth, Cancer Res, vol.38, pp.4155-4171, 1978.

N. Resnick, Platelet-derived growth factor B chain promoter contains a cis-acting fluid shear-stressresponsive element, Proc Natl Acad Sci, pp.4591-4595, 1993.

C. M. Ghajar and M. J. Bissell, Extracellular matrix control of mammary gland morphogenesis and tumorigenesis: insights from imaging, Histochemistry and Cell Biology, vol.163, issue.Pt 1, pp.1105-1118, 2008.
DOI : 10.1007/s00418-008-0537-1

E. Farge, Mechanotransduction in Development, Curr Top Dev Biol, vol.95, pp.243-65, 2011.
DOI : 10.1016/B978-0-12-385065-2.00008-6

T. Mammoto, D. J. Ingber, J. Yao, and H. Joshi, Mechanical control of tissue and organ developmentAttachment and tension in the spindle assembly checkpoint, Development. Journal of Cell Science, vol.137, issue.18, pp.1407-1427, 2002.

J. Zhou, J. Yao, and H. Joshi, Attachment and tension in the spindle assembly checkpoint, Journal of Cell Science, vol.115, issue.18, 2002.
DOI : 10.1242/jcs.00029

F. Le-noble, D. Moyon, L. Pardanaud, L. Yuan, V. Djonov et al., Flow regulates arterial-venous differentiation in the chick embryo yolk sac, Development, vol.131, issue.2, pp.361-375, 2004.
DOI : 10.1242/dev.00929

L. Adamo, O. Naveiras, P. L. Wenzel, S. Mckinney-freeman, P. J. Mack et al., Biomechanical forces promote embryonic haematopoiesis, Nature, vol.80, issue.7250, pp.1131-1135, 2009.
DOI : 10.1038/nature08073

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782763

V. L. Horner and M. F. Wolfner, Transitioning from egg to embryo: Triggers and mechanisms of egg activation, Developmental Dynamics, vol.49, issue.3, pp.527-544, 2008.
DOI : 10.1002/dvdy.21454

R. A. Foty and M. S. Steinberg, The differential adhesion hypothesis: a direct evaluation, Developmental Biology, vol.278, issue.1, pp.255-263, 2005.
DOI : 10.1016/j.ydbio.2004.11.012

M. Krieg, Y. Arboleda-estudillo, P. H. Puech, J. Kafer, F. Graner et al., Tensile forces govern germ-layer organization in zebrafish, Nature Cell Biology, vol.82, issue.4, pp.429-436, 2008.
DOI : 10.1007/s10237-006-0046-x

M. Allen, R. Rudd, M. Mcelfresh, and R. Balhorn, Time-dependent measure of a nanoscale force-pulse driven by the axonemal dynein motors in individual live sperm cells, Nanomedicine: Nanotechnology, Biology and Medicine, vol.6, issue.4, pp.510-525, 2010.
DOI : 10.1016/j.nano.2009.12.003

C. Brokaw, Direct measurements of sliding between outer doublet microtubules in swimming sperm flagella, Science, vol.243, issue.4898, pp.1593-96, 1989.
DOI : 10.1126/science.2928796

A. Boccaccio, M. Frassanito, L. Lamberti, R. Brunelli, and G. Maulucci, Nanoscale characterization of the biomechanical hardening of bovine zona pellucida, Journal of The Royal Society Interface, vol.249, issue.6, pp.2871-82, 2012.
DOI : 10.1002/jemt.20301

S. Reinsch and P. Gonczy, Mechanisms of nuclear positioning, J. Cell Sci. 111Pt, vol.16, pp.2283-95, 1998.

A. Desai and T. Mitchison, MICROTUBULE POLYMERIZATION DYNAMICS, Annual Review of Cell and Developmental Biology, vol.13, issue.1, pp.83-117, 1997.
DOI : 10.1146/annurev.cellbio.13.1.83

C. Kozlowski, M. Srayko, and F. Nedelec, Cortical Microtubule Contacts Position the Spindle in C. elegans Embryos, Cell, vol.129, issue.3, pp.499-510, 2007.
DOI : 10.1016/j.cell.2007.03.027

Y. Wang and V. Riechmann, The Role of the Actomyosin Cytoskeleton in Coordination of Tissue Growth during Drosophila Oogenesis, Current Biology, vol.17, issue.15, pp.1349-1355, 2007.
DOI : 10.1016/j.cub.2007.06.067

S. Nonaka, H. Shiratori, Y. Saijoh, and H. Hamada, Determination of left???right patterning of the mouse embryo by artificial nodal flow, Nature, vol.118, issue.6893, pp.96-99, 2002.
DOI : 10.1083/JCB.151.3.709

Y. Tanaka, Y. Okada, and N. Hirokawa, FGF-induced vesicular release of Sonic hedgehog and retinoic acid in leftward nodal flow is critical for left???right determination, Nature, vol.225, issue.7039, pp.172-177, 2005.
DOI : 10.1016/0006-8993(92)91557-U

M. Costa, D. Sweeton, and E. Wieschaus, 1993Gastrulation in Drosophila: cellular mechanisms of morphogenetic movements, The Development of Drosophila, pp.425-465

J. Colas and G. Schoenwolf, Towards a cellular and molecular understanding of neurulation, Developmental Dynamics, vol.215, issue.2, pp.117-162, 2001.
DOI : 10.1002/dvdy.1144

A. Jacinto, W. Wood, S. Woolner, C. Hiley, L. Turner et al., Dynamic Analysis of Actin Cable Function during Drosophila Dorsal Closure, Current Biology, vol.12, issue.14, pp.1245-1250, 2002.
DOI : 10.1016/S0960-9822(02)00955-7

D. Gospodarowicz and G. Greenburg, Determination of cellular shape by the extracellular matrix and its correlation with the control of cellular growth, Cancer Res, vol.38, pp.4155-4171, 1978.

M. Nakache and H. E. Gaub, Hydrodynamic hyperpolarization of endothelial cells., Proceedings of the National Academy of Sciences, vol.85, issue.6, pp.1841-1843, 1988.
DOI : 10.1073/pnas.85.6.1841

A. D. Bershadsky, N. Q. Balaban, and B. Geiger, Adhesion-Dependent Cell Mechanosensitivity, Annual Review of Cell and Developmental Biology, vol.19, issue.1, pp.677-695, 2003.
DOI : 10.1146/annurev.cellbio.19.111301.153011

L. E. Dike, C. S. Chen, M. Mrksich, J. Tien, G. M. Whitesides et al., Geometric control of switching between growth, apoptosis, and differentiation during angiogenesis using micropatterned substrates, In Vitro Cellular & Developmental Biology - Animal, vol.16, issue.8, pp.441-448, 1999.
DOI : 10.1007/s11626-999-0050-4

C. Ghajar and M. Bissell, Extracellular matrix control of mammary gland morphogenesis and tumorigenesis: insights from imaging, Histochemistry and Cell Biology, vol.163, issue.Pt 1, pp.1105-1123, 2008.
DOI : 10.1007/s00418-008-0537-1

D. Mitrossilis, J. Fouchard, D. Pereira, F. Postic, A. Richert et al., 2010 Real-time single-cell response to stiffness, pp.16518-16541

A. Saez, M. Ghibaudo, A. Buguin, P. Silberzan, and B. Ladoux, Rigidity-driven growth and migration of epithelial cells on microstructured anisotropic substrates, Proceedings of the National Academy of Sciences, vol.104, issue.20, pp.8281-8287, 2007.
DOI : 10.1073/pnas.0702259104

Q. Tseng, E. Duchemin-pelletier, A. Deshiere, M. Balland, H. Guillou et al., 2012 Spatial organization of the extracellular matrix regulates cell-cell junction positioning, Proc Natl Acad Sci, vol.1095, pp.1506-1517

C. Rauch, A. C. Brunet, J. Deleule, and E. Farge, C2C12 myoblast/osteoblast transdifferentiation steps enhanced by epigenetic inhibition of BMP2 endocytosis, AJP: Cell Physiology, vol.283, issue.1, pp.235-243, 2002.
DOI : 10.1152/ajpcell.00234.2001

A. J. Engler, S. Sen, H. L. Sweeney, and D. E. Discher, Matrix Elasticity Directs Stem Cell Lineage Specification, Cell, vol.126, issue.4, pp.677-689, 2006.
DOI : 10.1016/j.cell.2006.06.044

URL : http://doi.org/10.1016/j.cell.2006.06.044

R. Mcbeath, D. Pirone, C. Nelson, K. Bhadriraju, and C. Chen, Cell Shape, Cytoskeletal Tension, and RhoA Regulate Stem Cell Lineage Commitment, Developmental Cell, vol.6, issue.4, pp.483-95, 2004.
DOI : 10.1016/S1534-5807(04)00075-9

A. Buxboim, I. L. Ivanovska, and D. E. Discher, Matrix elasticity, cytoskeletal forces and physics of the nucleus: how deeply do cells 'feel' outside and in?, Journal of Cell Science, vol.123, issue.3, pp.297-308, 2010.
DOI : 10.1242/jcs.041186

G. V. Shivashankar, Mechanosignaling to the Cell Nucleus and Gene Regulation, Annual Review of Biophysics, vol.40, issue.1, pp.361-378, 2011.
DOI : 10.1146/annurev-biophys-042910-155319

D. N. Simon, W. , and K. L. , The nucleoskeleton as a genome-associated dynamic 'network of networks', Nature Reviews Molecular Cell Biology, vol.18, issue.11, pp.695-708, 2011.
DOI : 10.1038/nrm3207

N. Wang, J. D. Tytell, and D. E. Ingber, Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus, Nature Reviews Molecular Cell Biology, vol.12, issue.1, pp.75-82, 2009.
DOI : 10.1038/nrm2594

Y. Wang and V. Riechmann, The Role of the Actomyosin Cytoskeleton in Coordination of Tissue Growth during Drosophila Oogenesis, Current Biology, vol.17, issue.15, pp.1349-1355, 2007.
DOI : 10.1016/j.cub.2007.06.067

C. M. Nelson, Emergent patterns of growth controlled by multicellular form and mechanics, Proc. Natl Acad. Sci. USA, pp.11594-11599, 2005.
DOI : 10.1073/pnas.0502575102

P. Pouille, P. Ahmadi, A. Brunet, and E. Farge, Mechanical signals trigger Myosin II redistribution and mesoderm invagination in Drosophila embryos. Sci Signal, 2009.

R. Fernandez-gonzalez, S. Sde, M. Röper, J. Eaton, S. Zallen et al., Myosin II Dynamics Are Regulated by Tension in Intercalating Cells, Developmental Cell, vol.17, issue.5, pp.736-779, 2009.
DOI : 10.1016/j.devcel.2009.09.003

J. R. Hove, R. W. Koster, A. S. Forouhar, G. Acevedo-bolton, S. E. Fraser et al., Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis, Nature, vol.203, issue.6919, pp.172-177, 2003.
DOI : 10.1007/s003480050366

D. A. Voronov, P. W. Alford, G. Xu, and L. A. Taber, The role of mechanical forces in dextral rotation during cardiac looping in the chick embryo, Developmental Biology, vol.272, issue.2, pp.339-350, 2004.
DOI : 10.1016/j.ydbio.2004.04.033

Q. Chen, L. Jiang, C. Li, D. Hu, and J. Bu, Haemodynamics-Driven Developmental Pruning of Brain Vasculature in Zebrafish, PLoS Biology, vol.10, issue.8, p.1001374, 2012.
DOI : 10.1371/journal.pbio.1001374.s025

J. Kahn, Y. Shwartz, E. Blitz, S. Krief, A. Sharir et al., Muscle Contraction Is Necessary to Maintain Joint Progenitor Cell Fate, Developmental Cell, vol.16, issue.5, pp.734-777, 2009.
DOI : 10.1016/j.devcel.2009.04.013

B. Driquez, A. Bouclet, and E. Farge, Mechanotransduction in Drosophila embryo mesoderm invagination: transition from individual pulsating to collective constriction behaviour 52 Mechanotransduction in mechanically coupled pulsating cells: transition to collective constriction and mesoderm invagination simulation, Phys Biol, vol.88, issue.66, pp.66007-66017, 2011.

M. Costa, E. Wilson, and E. Wieschaus, A putative cell signal encoded by the folded gastrulation gene coordinates cell shape changes during Drosophila gastrulation, Cell, vol.76, issue.6, pp.1075-89, 1994.
DOI : 10.1016/0092-8674(94)90384-0

T. C. Seher, M. Narasimha, E. Vogelsang, and M. Leptin, Analysis and reconstitution of the genetic cascade controlling early mesoderm morphogenesis in the Drosophila embryo, Mechanisms of Development, vol.124, issue.3, pp.167-79, 2007.
DOI : 10.1016/j.mod.2006.12.004

A. C. Martin, M. Kaschube, and E. Wieschaus, Pulsed contractions of an actin???myosin network drive apical constriction, Nature, vol.33, issue.7228, pp.495-504, 2009.
DOI : 10.1038/nature07522

M. Koehl, Biomechanical approaches to morphogenesis, Sem Dev Biol, vol.1, pp.367-378, 1990.

L. Taber, Biomechanics of Growth, Remodeling, and Morphogenesis, Applied Mechanics Reviews, vol.48, issue.8, p.48, 1995.
DOI : 10.1115/1.3005109

E. Farge, Mechanical Induction of Twist in the Drosophila Foregut/Stomodeal Primordium, Current Biology, vol.13, issue.16, pp.1365-1377, 2003.
DOI : 10.1016/S0960-9822(03)00576-1

V. Vogel and M. Sheetz, Local force and geometry sensing regulate cell functions, Nature Reviews Molecular Cell Biology, vol.31, issue.4, pp.265-275, 2006.
DOI : 10.1016/S0022-2836(02)01001-X

M. Wozniak and C. Chen, Mechanotransduction in development: a growing role for contractility, Nature Reviews Molecular Cell Biology, vol.10, issue.1, pp.34-43, 2009.
DOI : 10.1038/nrm2592

T. Mammoto and D. Ingber, Mechanical control of tissue and organ development, Development, vol.137, issue.9, pp.1407-1420
DOI : 10.1242/dev.024166

G. M. Odell, G. Oster, and B. Burnside, The mechanical basis of morphogenesis. I. Epithelial folding and invagination, Dev. Biol, 1981.

K. Sherrard, F. Robin, P. Lemaire, and . Munro, Sequential Activation of Apical and Basolateral Contractility Drives Ascidian Endoderm Invagination, Current Biology, vol.20, issue.17, pp.1499-1510, 2010.
DOI : 10.1016/j.cub.2010.06.075

URL : https://hal.archives-ouvertes.fr/hal-00566790

L. A. Davidson, M. A. Koehl, R. Keller, and G. F. Oster, How do sea urchins invaginate? Using biomechanics to distinguish between mechanisms of primary invagination, Development, vol.121, 1995.

J. J. Munoz, K. Barrett, and M. Miodownik, A deformation gradient decomposition method for the analysis of the mechanics of morphogenesis, Journal of Biomechanics, vol.40, issue.6, pp.1372-1380, 2007.
DOI : 10.1016/j.jbiomech.2006.05.006

V. Conte, J. J. Mun?oz, and M. Miodownik, A 3D finite element model of ventral furrow invagination in the Drosophila melanogaster embryo, Journal of the Mechanical Behavior of Biomedical Materials, vol.1, issue.2, pp.188-198, 2008.
DOI : 10.1016/j.jmbbm.2007.10.002

P. A. Pouille and E. Farge, Hydrodynamic simulation of multicellular embryo invagination, Physical Biology, vol.5, issue.1, p.15005, 2008.
DOI : 10.1088/1478-3975/5/1/015005

V. Conte, J. J. Mun?oz, and M. Miodownik, Robust mechanisms of ventral furrow invagination require the combination of cellular shape changes, Physical Biology, vol.6, issue.1, p.16010, 2009.
DOI : 10.1088/1478-3975/6/1/016010

V. Conte, F. Ulrich, and M. Miodownik, A Biomechanical Analysis of Ventral Furrow Formation in the Drosophila Melanogaster Embryo, PLoS ONE, vol.10, issue.18407, p.34473, 2012.
DOI : 10.1371/journal.pone.0034473.s016

G. W. Brodland, V. Conte, and M. Miodownik, Video force microscopy reveals the mechanics of ventral furrow invagination in Drosophila, Proc. Natl. Acad. Sci. USA, pp.22111-22116, 2010.
DOI : 10.1073/pnas.1006591107

H. Brezav_s_cek, A. , and M. Rauzi, A Model of Epithelial Invagination Driven by Collective Mechanics of Identical Cells, Biophysical Journal, vol.103, issue.5, pp.1069-1077, 2012.
DOI : 10.1016/j.bpj.2012.07.018

A. Alberga, J. L. Boulay, and E. Kempe, Dennefeld C and Haenlin M 1991The snail gene required for mesoderm formation in Drosophila is expressed dynamically in derivatives of all three germ layers Development, pp.983-92

A. Martin, Pulsation and stabilization: Contractile forces that underlie morphogenesis, Developmental Biology, vol.341, issue.1, pp.114-139, 2009.
DOI : 10.1016/j.ydbio.2009.10.031

URL : http://doi.org/10.1016/j.ydbio.2009.10.031

Z. Kam, J. S. Minden, D. A. Agard, J. W. Sedat, and M. Leptin, Drosophila gastrulation: analysis of cell shape changes in living embryos by three-dimensional fluorescence microscopy Development, pp.365-70, 1991.

J. Solon, A. Kaya-copur, J. Colombelli, and D. Brunner, Pulsed Forces Timed by a Ratchet-like Mechanism Drive Directed Tissue Movement during Dorsal Closure, Cell, vol.137, issue.7, pp.1331-1373, 2009.
DOI : 10.1016/j.cell.2009.03.050

R. E. Dawes-hoang, K. M. Parmar, A. E. Christiansen, C. B. Phelps, A. Brand et al., Folded gastrulation , cell shape change and the control of myosin localization Development, pp.4165-787, 2005.

J. K. Sawyer, N. J. Harris, K. C. Slep, U. Gaul, and M. Peifer, afadin homologue Canoe regulates linkage of the actin cytoskeleton to adherens junctions during apical constriction, The Journal of Cell Biology, vol.112, issue.1, pp.57-73, 2009.
DOI : 10.1016/S0960-9822(99)80392-3

T. Brunet, A. Bouclet, P. Ahmadi, D. Mitrossilis, B. Driquez et al., Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria 81 Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria, Nat Commun, vol.4, pp.2821-2831, 2013.

E. Farge, Mechanical Induction of Twist in the Drosophila Foregut/Stomodeal Primordium, Current Biology, vol.13, issue.16, pp.1365-1377, 2003.
DOI : 10.1016/S0960-9822(03)00576-1

N. Desprat, W. Supatto, P. A. Pouille, E. Beaurepaire, E. Farge et al., Tissue Deformation Modulates Twist Expression to Determine Anterior Midgut Differentiation in Drosophila Embryos, Fluid shear stress induces betacatenin signaling in osteoblasts. Calcif Tissue Int, pp.470-477396, 2004.
DOI : 10.1016/j.devcel.2008.07.009

URL : https://hal.archives-ouvertes.fr/hal-00324225

J. Kahn, Y. Shwartz, E. Blitz, S. Krief, A. Sharir et al., Muscle Contraction Is Necessary to Maintain Joint Progenitor Cell Fate, Developmental Cell, vol.16, issue.5, pp.734-777, 2009.
DOI : 10.1016/j.devcel.2009.04.013

J. Whitehead, mouse colon, HFSP Journal, vol.2, issue.5, pp.286-294, 2008.
DOI : 10.2976/1.2955566

URL : https://hal.archives-ouvertes.fr/hal-00824412

M. S. Samuel, Actomyosin-Mediated Cellular Tension Drives Increased Tissue Stiffness and ??-Catenin Activation to Induce Epidermal Hyperplasia and Tumor Growth, Cancer Cell, vol.19, issue.6, pp.776-791, 2011.
DOI : 10.1016/j.ccr.2011.05.008

URL : http://doi.org/10.1016/j.ccr.2011.05.008

C. B. Kimmel and R. D. Law, Cell lineage of zebrafish blastomeres.. Cleavage pattern and cytoplasmic bridges between cells, Dev. Biol, pp.10878-85, 1985.

D. A. Kane, R. A. Warga, and C. B. Kimmel, Mitotic domains in the early embryo of the zebrafish, Nature, vol.360, issue.6406, pp.735-737, 1992.
DOI : 10.1038/360735a0

J. P. Trinkaus, The midblastula transition, the YSL transition and the onset of gastrulation in Fundulus, pp.75-80, 1992.

L. Solnica-krezel and W. Driever, Microtubule arrays of the zebrafish yolk cell: organization and function during epiboly, Development, vol.120, pp.2443-2455, 1994.

A. Wood and L. P. Timmermans, Teleost epiboly: reassessment of deep cell movement in the germ ring, Development, vol.102, pp.575-585, 1988.

E. Hanneman and M. Westerfield, Early expression of acetylcholinesterase activity in functionally distinct neurons of the zebrafish, The Journal of Comparative Neurology, vol.19, issue.3, pp.350-361, 1989.
DOI : 10.1002/cne.902840303

C. Thisse, B. Thisse, T. F. Schilling, and J. H. Postlethwait, Structure of the zebrafish snail1 gene and its expression in wildtype, spadetail and no tail mutant embryos, Development, vol.119, pp.1203-1215, 1993.

A. Agathon, C. Thisse, and &. Bernard-thisse, The molecular nature of the zebrafish tail organizer, Nature, vol.424, issue.6947, pp.448-452, 2003.
DOI : 10.1038/nature01822

W. W. Ballard, Morphogenetic Movements and Fate Maps of Vertebrates, American Zoologist, vol.21, issue.2, pp.391-399, 1981.
DOI : 10.1093/icb/21.2.391

S. J. Gould, Ontogeny and Phylogeny, 1977.

J. P. Reib, La circulation sanguine chez I'embryon de Bruchyd a n ~ ore rio, Ann. Embryol. Morphol, vol.6, pp.43-54, 1973.

N. Milos and A. D. Dingle, Dynamics of pigment pattern formation in the zebrafish,Brachydanio rerio. I. Establishment and regulation of the lateral line melanophore stripe during the first eight days of development, Journal of Experimental Zoology, vol.134, issue.2, pp.205-216, 1978.
DOI : 10.1002/jez.1402050205

S. Schneider, H. Steinbeisser, R. M. Warga, and . Hausen, ??-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos, Mechanisms of Development, vol.57, issue.2, pp.191-198, 1996.
DOI : 10.1016/0925-4773(96)00546-1

E. M. De-robertis, Evo-Devo: Variations on Ancestral Themes, Cell, vol.132, issue.2, pp.185-195, 2008.
DOI : 10.1016/j.cell.2008.01.003

C. D. Stern, Gastrulation: From Cells to Embryo Cold, 2004.

A. Schohl and F. Fagotto, A role for maternal ??-catenin in early mesoderm induction in Xenopus, The EMBO Journal, vol.22, issue.13, pp.3303-3313, 2003.
DOI : 10.1093/emboj/cdg328

T. Valenta, Probing transcription-specific outputs of ??-catenin in vivo, Genes & Development, vol.25, issue.24, pp.2631-2643, 2011.
DOI : 10.1101/gad.181289.111

J. L. Lewis, Reiterated Wnt signaling during zebrafish neural crest development, Development, vol.131, issue.6, pp.1299-1308, 2004.
DOI : 10.1242/dev.01007

URL : http://dev.biologists.org/cgi/content/short/131/6/1299

S. Ueno, Biphasic role for Wnt/beta-catenin signaling in cardiac specification in zebrafish and embryonic stem cells, Proceedings of the National Academy of Sciences, vol.104, issue.23, pp.9685-9690, 2007.
DOI : 10.1073/pnas.0702859104

J. Kahn, Muscle Contraction Is Necessary to Maintain Joint Progenitor Cell Fate, Developmental Cell, vol.16, issue.5, pp.734-743, 2009.
DOI : 10.1016/j.devcel.2009.04.013

B. Sen, Mechanical Strain Inhibits Adipogenesis in Mesenchymal Stem Cells by Stimulating a Durable ??-Catenin Signal, Endocrinology, vol.149, issue.12, pp.6065-6075, 2008.
DOI : 10.1210/en.2008-0687

C. Fukazawa, poky/chuk/ikk1 is required for differentiation of the zebrafish embryonic epidermis, Developmental Biology, vol.346, issue.2, pp.272-283, 2010.
DOI : 10.1016/j.ydbio.2010.07.037

J. Limouze, A. F. Straight, T. Mitchison, and J. R. Sellers, Specificity of blebbistatin, an inhibitor of myosin II, Journal of Muscle Research and Cell Motility, vol.278, issue.4-5, pp.337-341, 2004.
DOI : 10.1007/s10974-004-6060-7

L. Solnica-krezel and W. Driever, Microtubule arrays of the zebrafish yolk cell: organization and function during epiboly, pp.2443-2455, 1994.

S. Schulte-merker, Expression of zebrafish goosecoid and no tail gene products in wild-type and mutant no tail embryos, Development, vol.120, pp.843-852, 1994.

S. E. Stachel, D. J. Grunwald, and P. Myers, Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish, Development, vol.117, pp.1261-1274, 1993.

E. M. De-robertis, Dismantling the organizer, Nature, vol.374, issue.6521, pp.407-408, 1995.
DOI : 10.1038/374407a0

N. M. Dempsey, High performance hard magnetic NdFeB thick films for integration into micro-electro-mechanical systems, Applied Physics Letters, vol.90, issue.9, pp.92509-92510, 2007.
DOI : 10.1063/1.2710771

URL : https://hal.archives-ouvertes.fr/hal-00139182

G. Bealle, Ultra Magnetic Liposomes for MR Imaging, Targeting, and Hyperthermia, Langmuir, vol.28, issue.32, pp.11834-11842, 2012.
DOI : 10.1021/la3024716

M. R. Rebagliati, R. Toyama, C. Fricke, P. Haffter, and I. B. Dawid, Zebrafish Nodal-Related Genes Are Implicated in Axial Patterning and Establishing Left???Right Asymmetry, Developmental Biology, vol.199, issue.2, pp.261-272, 1998.
DOI : 10.1006/dbio.1998.8935

B. Feldman, organizer development and germ-layer formation require nodal-related signals, Zebrafish Nature, vol.395, pp.181-185, 1998.

E. G. Hagos and S. Dougan, Time-dependent patterning of the mesoderm and endoderm by Nodal signals in zebrafish, BMC Developmental Biology, vol.7, issue.1, pp.1-22, 2007.
DOI : 10.1186/1471-213X-7-22

C. Thisse and B. Thisse, Antivin, a novel and divergent member of the TGF? superfamily , negatively regulates mesoderm induction, Development, vol.126, pp.229-240, 1999.

W. Van-veelen, ??-catenin tyrosine 654 phosphorylation increases Wnt signalling and intestinal tumorigenesis, Gut, vol.60, issue.9, pp.1204-1212, 2011.
DOI : 10.1136/gut.2010.233460

M. Leptin, twist and snail as positive and negative regulators during Drosophila mesoderm development., Genes & Development, vol.5, issue.9, pp.1568-76, 1991.
DOI : 10.1101/gad.5.9.1568

URL : http://genesdev.cshlp.org/cgi/content/short/5/9/1568

E. Brouzés and E. Farge, Interplay of mechanical deformation and patterned gene expression in developing embryos, Current Opinion in Genetics & Development, vol.14, issue.4, pp.367-74, 2004.
DOI : 10.1016/j.gde.2004.06.005

L. Leptin, M. Grunewald, and B. , Cell shape changes during gastrulation in Drosophila, Development, vol.110, pp.73-84, 1990.

M. Peifer, D. Sweeton, M. Casey, and E. Wieschaus, Wingless signal and Zestewhite 3 kinase trigger opposing changes in the intracellular distribution of Armadillo, Development, vol.120, pp.369-380, 1994.

M. Takahashi, F. Takahashi, K. Ui-tei, T. Kojima, and K. Saigo, Requirements of genetic interactions between Src42A, armadillo and shotgun, a gene encoding E-cadherin, for normal development in Drosophila, Development, vol.132, issue.11, pp.2547-2559, 2005.
DOI : 10.1242/dev.01850

M. Q. Martindale, K. Pang, and J. R. Finnerty, Investigating the origins of triploblasty: `mesodermal' gene expression in a diploblastic animal, the sea anemone Nematostella vectensis (phylum, Cnidaria; class, Anthozoa), Development, vol.131, issue.10, pp.2463-2474, 2004.
DOI : 10.1242/dev.01119

A. Schohl and F. Fagotto, A role for maternal ??-catenin in early mesoderm induction in Xenopus, The EMBO Journal, vol.22, issue.13, pp.3303-3313, 2003.
DOI : 10.1093/emboj/cdg328

S. A. Harvey, S. Tumpel, J. Dubrulle, A. F. Schier, and J. Smith, no tail integrates two modes of mesoderm induction, Development, vol.137, issue.7, pp.1127-113510, 2010.
DOI : 10.1242/dev.046318

R. E. Keller, The cellular basis of epiboly: an SEM study of deep-cell rearrangement during gastrulation in Xenopus laevis, J. Embryol. Exp. Morphol, vol.60, pp.201-234, 1980.

E. S. Kornikova, T. G. Troshina, S. V. Kremnyov, and L. V. Beloussov, Neuro-mesodermal patterns in artificially deformed embryonic explants: A role for mechano-geometry in tissue differentiation, Developmental Dynamics, vol.125, issue.3, pp.885-896, 2010.
DOI : 10.1002/dvdy.22238

J. M. Gross and D. R. Mcclay, The Role of Brachyury (T) during Gastrulation Movements in the Sea Urchin Lytechinus variegatus, Developmental Biology, vol.239, issue.1, pp.132-147, 2001.
DOI : 10.1006/dbio.2001.0426

C. D. Stern, Gastrulation: From Cells to Embryo Cold, 2004.

T. Valenta, Probing transcription-specific outputs of ??-catenin in vivo, Genes & Development, vol.25, issue.24, pp.2631-2643, 2011.
DOI : 10.1101/gad.181289.111

M. Sharma, C. Jamieson, M. Johnson, M. P. Molloy, and B. R. Henderson, Specific Armadillo Repeat Sequences Facilitate ??-Catenin Nuclear Transport in Live Cells via Direct Binding to Nucleoporins Nup62, Nup153, and RanBP2/Nup358, Journal of Biological Chemistry, vol.287, issue.2, pp.819-831
DOI : 10.1074/jbc.M111.299099

P. Polakis, 2012 Wnt signaling in cancer, Cold Spring Harb. Perspect. Biol, vol.4, pp.1-13

M. Tamada, D. L. Farrell, and J. A. Zallen, Abl Regulates Planar Polarized Junctional Dynamics through ??-Catenin Tyrosine Phosphorylation, Developmental Cell, vol.22, issue.2, pp.309-319
DOI : 10.1016/j.devcel.2011.12.025

URL : http://doi.org/10.1016/j.devcel.2011.12.025

M. S. Samuel, Actomyosin-Mediated Cellular Tension Drives Increased Tissue Stiffness and ??-Catenin Activation to Induce Epidermal Hyperplasia and Tumor Growth, Cancer Cell, vol.19, issue.6, pp.776-791, 2011.
DOI : 10.1016/j.ccr.2011.05.008

URL : http://doi.org/10.1016/j.ccr.2011.05.008

D. Arendt and K. Nu¨bler-jung, Dorsal or ventral: Similarities in fate maps and gastrulation patterns in annelids, arthropods and chrodates, Mechanisms of Development, vol.61, issue.1-2, pp.7-21, 1997.
DOI : 10.1016/S0925-4773(96)00620-X

D. J. Dickinson, W. J. Nelson, and W. Weis, A Polarized Epithelium Organized by ??- and ??-Catenin Predates Cadherin and Metazoan Origins, Science, vol.331, issue.6022, pp.1336-1339
DOI : 10.1126/science.1199633

M. M. Shen, Nodal signaling: developmental roles and regulation, Development, vol.134, issue.6, pp.1023-1034, 2007.
DOI : 10.1242/dev.000166

J. A. Lynch and S. Roth, The evolution of dorsal-ventral patterning mechanisms in insects, Genes & Development, vol.25, issue.2, pp.107-118, 2011.
DOI : 10.1101/gad.2010711

E. J. Douzery, E. A. Snell, E. Bapteste, F. Delsuc, and H. Philippe, The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils?, Proc. Natl Acad. Sci. USA, pp.15386-15391, 2004.
DOI : 10.1073/pnas.0403984101

URL : https://hal.archives-ouvertes.fr/halsde-00193035

K. J. Peterson, Estimating metazoan divergence times with a molecular clock, Proc. Natl Acad. Sci. USA 101, pp.6536-6541, 2004.
DOI : 10.1073/pnas.0401670101

S. I. Grewal and J. C. Rice, Regulation of heterochromatin by histone methylation and small RNAs, Current Opinion in Cell Biology, vol.16, issue.3, pp.230-238, 2004.
DOI : 10.1016/j.ceb.2004.04.002

S. B. Carroll, S. R. Wessler, A. J. Griffiths, . Lewontin, and C. Richard, Introduction to genetic analysis, p.403, 2008.

K. Sato and M. Siomi, Piwi-interacting RNAs: biological functions and biogenesis, Essays In Biochemistry, vol.2, pp.39-52, 2013.
DOI : 10.1242/dev.01809

A. De-vanssay, A. Bougé, A. Boivin, C. Hermant, and L. Teysset, Paramutation in Drosophila linked to emergence of a piRNA-producing locus, Nature, vol.10, issue.7418, pp.112-115
DOI : 10.1038/nature11416

C. Biemont and C. Vieira, Genetics: Junk DNA as an evolutionary force, Nature, vol.2, issue.7111, pp.521-524, 2006.
DOI : 10.1159/000084978

E. S. Lander, L. M. Linton, B. Birren, C. Nusbaum, M. C. Zody et al., Initial sequencing and analysis of the human genome, Nature, vol.6, issue.6822, pp.860-921, 2001.
DOI : 10.1038/35057062

D. J. Finnegan, Retrotransposons, Current Biology, vol.22, issue.11, pp.432-437, 2012.
DOI : 10.1016/j.cub.2012.04.025

URL : http://doi.org/10.1016/j.cub.2012.04.025

E. Gogvadze and A. Buzdin, Retroelements and their impact on genome evolution and functioning, Cellular and Molecular Life Sciences, vol.35, issue.suppl 2, pp.3727-3742, 2009.
DOI : 10.1007/s00018-009-0107-2

P. A. Callinan and M. A. Batzer, Retrotransposable Elements and Human Disease, Genome Dyn, vol.1, pp.104-115, 2006.
DOI : 10.1159/000092503

J. Brennecke, Discrete Small RNA-Generating Loci as Master Regulators of Transposon Activity in Drosophila, Cell, vol.128, issue.6, pp.1089-1103, 2007.
DOI : 10.1016/j.cell.2007.01.043

C. Mikiko and A. Siomi-kaoru-sato-dubravka-pezic-alexei, Aravin 2011 PIWI-interacting small RNAs: the vanguard of genome defence, Nature Reviews Molecular Cell Biology, vol.12, pp.246-258

L. S. Gunawardane, A Slicer-Mediated Mechanism for Repeat-Associated siRNA 5' End Formation in Drosophila, Science, vol.315, issue.5818, pp.1587-1590, 2007.
DOI : 10.1126/science.1140494

N. Masrouha, L. Yang, S. Hijal, S. Larochelle, and B. Suter, The Drosophila chk2 gene loki is essential for embryonic DNA double-strand-break checkpoints induced in S phase or G2, Genetics, vol.163, pp.973-982, 2003.

M. Yamaguchi, N. Fujimori-tonou, and Y. Kishi, Hitoshi Okamoto and Ichiro Masai 2008 Mutation of DNA primase causes extensive apoptosis of retinal neurons through the activation of DNA damage checkpoint and tumor suppressor p53 Development135, pp.1247-1257

T. Takanami, S. Sato, T. Ishihara, I. Katsura, H. Takahashi et al., Characterization of a Caenorhabditis elegans recA-like gene Ce-rdh-1 involved in meiotic recombina-DNA Res, pp.373-377, 1998.

A. Gartner, S. Milstein, S. Ahmed, J. Hodgkin, and M. O. Hengartner, A Conserved Checkpoint Pathway Mediates DNA Damage???Induced Apoptosis and Cell Cycle Arrest in C. elegans, Molecular Cell, vol.5, issue.3, pp.435-443, 2000.
DOI : 10.1016/S1097-2765(00)80438-4

W. Edelman, P. E. Cohen, M. Kane, K. Lau, B. Morrow et al., Meiotic Pachytene Arrest in MLH1-Deficient Mice, Cell, vol.85, issue.7, pp.1125-1134, 1996.
DOI : 10.1016/S0092-8674(00)81312-4

D. L. Pittman, J. Cobb, K. J. Schimenti, L. A. Wilson, D. M. Cooper et al., Meiotic Prophase Arrest with Failure of Chromosome Synapsis in Mice Deficient for Dmc1, a Germline-Specific RecA Homolog, Molecular Cell, vol.1, issue.5, pp.697-705, 1998.
DOI : 10.1016/S1097-2765(00)80069-6

M. Brodsky, W. Nordstrom, G. Tsang, E. Kwan, G. Rubin et al., Drosophila p53 Binds a Damage Response Element at the reaper Locus, Cell, vol.101, issue.1, pp.103-113, 2000.
DOI : 10.1016/S0092-8674(00)80627-3

M. Ollmann, L. Young, D. Como, C. Karim, F. Belvin et al., Drosophila p53 Is a Structural and Functional Homolog of the Tumor Suppressor p53, Cell, vol.101, issue.1, pp.91-101, 2000.
DOI : 10.1016/S0092-8674(00)80626-1

S. Titen, H. Lin, J. Bhandari, and K. Golic, Chk2 and P53 Regulate the Transmission of Healed Chromosomes in the Drosophila Male Germline, PLoS Genetics, vol.37, issue.2, p.1004130
DOI : 10.1371/journal.pgen.1004130.t007

C. Klattenhoff, D. Bratu, N. Mcginnis-schultz, B. Koppetsch, H. Cook et al., Drosophila rasiRNA Pathway Mutations Disrupt Embryonic Axis Specification through Activation of an ATR/Chk2 DNA Damage Response, Developmental Cell, vol.12, issue.1, pp.45-55, 2007.
DOI : 10.1016/j.devcel.2006.12.001

Y. Chen, A. Pane, and T. Schüpbach, cutoff and aubergine Mutations Result in Retrotransposon Upregulation and Checkpoint Activation in Drosophila, Current Biology, vol.17, issue.7, pp.1-6, 2007.
DOI : 10.1016/j.cub.2007.02.027

A. Pane, K. Wehr, and T. Schüpbach, zucchini and squash Encode Two Putative Nucleases Required for rasiRNA Production in the Drosophila Germline, Developmental Cell, vol.12, issue.6, pp.851-862
DOI : 10.1016/j.devcel.2007.03.022

P. Fichelson, M. Jagut, S. Lepanse, J. Lepesant, and J. Huynh, lethal giant larvae is required with the par genes for the early polarization of the Drosophila oocyte, Development, vol.137, issue.5, pp.815-839
DOI : 10.1242/dev.045013

URL : https://hal.archives-ouvertes.fr/hal-00484574

K. Olsen, T. Reynolds, A. Ary, and . Hoffmann, A field cage test of the effects of the endosymbiont Wolbachia on Drosophila melanogaster, Heredity, vol.86, issue.6, pp.731-737, 2001.
DOI : 10.1046/j.1365-2540.2001.00892.x

E. Wieschaus, J. Marsh, and W. Gehring, fs(1) K10, a germ-line dependent female ste-rile mutation causling abnormal chorion morphology in Drosophila melanogaster, Arch Dev Biol, vol.1, issue.84, pp.978-75