T. Akagi, I. M. Henry, R. Tao, and L. Comai, A Y-chromosome-encoded small RNA acts as a sex determinant in persimmons, Science, vol.346, pp.646-650, 2014.
DOI : 10.1126/science.1257225

T. L. Ashman, J. A. Tennessen, R. M. Dalton, R. Govindarajulu, M. H. Koski et al., Multilocus Sex Determination Revealed in Two Populations of Gynodioecious Wild Strawberry, Fragaria vesca subsp. bracteata, G3 (Bethesda), vol.5, pp.2759-2773, 2015.
DOI : 10.1101/023713

URL : https://www.biorxiv.org/content/early/2015/08/02/023713.full.pdf

D. Bachtrog, Sex determination: why so many ways of doing it?, In: PLoS Biol, vol.12, p.1001899, 2014.
DOI : 10.1371/journal.pbio.1001899

URL : https://doi.org/10.1371/journal.pbio.1001899

S. C. Barrett, The evolution of plant sexual diversity, In: Nature reviews. Genetics, vol.3, issue.4, pp.274-84, 2002.

G. Bernasconi, Silene as a model system in ecology and evolution, Heredity (Edinb), vol.103, pp.5-14, 2009.
DOI : 10.1038/hdy.2009.34

URL : https://hal.archives-ouvertes.fr/hal-00428347

A. Boualem, A cucurbit androecy gene reveals how unisexual flowers develop and dioecy emerges, Science, vol.350, pp.688-691, 2015.
DOI : 10.1126/science.aac8370

URL : http://prodinra.inra.fr/ft/4B022E65-1B14-4E84-8DB3-A6060FA91AB8

B. Charlesworth and D. Charlesworth, A Model for the Evolution of Dioecy and Gynodioecy, The American Naturalist, vol.112, pp.975-997, 1978.

D. Charlesworth, Theories of the Evolution of Dioecy, Gender and Sexual Dimorphism in Flowering Plants, pp.33-60, 1999.

E. L. Charnov, The theory of sex allocation, Monogr Popul Biol, vol.18, pp.1-355, 1982.

L. F. Delph, P. Touzet, and M. F. Bailey, Merging theory and mechanism in studies of gynodioecy, Trends Ecol. Evol. (Amst.), vol.22, issue.1, pp.17-24, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00091798

C. Desfeux, S. Maurice, J. P. Henry, B. Lejeune, and P. H. Gouyon, Evolution of reproductive systems in the genus Silene, Proc. Biol. Sci, vol.263, pp.409-414, 1996.
URL : https://hal.archives-ouvertes.fr/halsde-00350999

M. Dufay, P. Champelovier, J. Käfer, J. P. Henry, S. Mousset et al., An angiosperm-wide analysis of the gynodioecy-dioecy pathway, Annals of Botany, vol.114, pp.539-548, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01110834

B. K. Ehlers and T. Bataillon, Inconstant males' and the maintenance of labile sex expression in subdioecious plants, New Phytol, vol.174, pp.194-211, 2007.

E. M. Golenberg and N. W. West, Hormonal interactions and gene regulation can link monoecy and environmental plasticity to the evolution of dioecy in plants, In: American Journal of Botany, vol.100, pp.1022-1037, 2013.

R. Hobza, E. Kejnovsky, B. Vyskot, and A. Widmer, The role of chromosomal rearrangements in the evolution of Silene latifolia sex chromosomes, Molecular Genetics and Genomics, vol.278, pp.633-638, 2007.

J. Käfer, G. A. Marais, and J. R. Pannell, On the rarity of dioecy in flowering plants, Mol. Ecol, vol.26, pp.1225-1241, 2017.

R. Li, J. Li, G. Yin, J. Yang, W. Zou et al., A male-specific SCAR DNA marker and sex ratio of seedlings in salak (Salacca zalacca var. zalacca)". In: Journal of, Forestry Research, vol.28, pp.47-50, 2017.

C. K. Matson and D. Zarkower, Sex and the singular DM domain: insights into sexual regulation, evolution and plasticity, Nat. Rev. Genet, vol.13, issue.3, pp.163-174, 2012.
DOI : 10.1038/nrg3161

URL : http://europepmc.org/articles/pmc3595575?pdf=render

S. Maurice, D. Belhassen, P. H. Couvet, and . Gouyon, Evolution of dioecy: can nuclear-cytoplasmic interactions select for maleness?, In: Heredity, vol.73, pp.346-54, 1993.
URL : https://hal.archives-ouvertes.fr/halsde-00351200

R. Ming, A. Bendahmane, and S. S. Renner, Sex chromosomes in land plants, In: Annual Review of Plant Biology, vol.62, issue.1, pp.485-514, 2011.
DOI : 10.1146/annurev-arplant-042110-103914

K. Murase, MYB transcription factor gene involved in sex determination in Asparagus officinalis, Genes to Cells, vol.22, pp.115-123, 2017.

A. Muyle, G. A. Shearn, and . Marais, The Evolution of Sex Chromosomes and Dosage Compensation in Plants, Genome Biology and Evolution, vol.9, pp.627-645, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01943816

J. R. Pannell, S. M. Eppley, M. E. Dorken, and R. Berjano, Regional variation in sex ratios and sex allocation in androdioecious Mercurialis annua, J. Evol. Biol, vol.27, pp.1467-1477, 2014.

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.

A. Rautenberg, L. Hathaway, B. Oxelman, and H. C. Prentice, Geographic and phylogenetic patterns in Silene section Melandrium (Caryophyllaceae) as inferred from chloroplast and nuclear DNA sequences, Mol. Phylogenet. Evol, vol.57, pp.978-991, 2010.

S. S. Renner, Pathways for making unisexual flowers and unisexual plants: Moving beyond the Two mutations linked on one chromosome model, American Journal of Botany, vol.103, pp.587-589, 2016.

S. S. Renner, The relative and absolute frequencies of angiosperm sexual systems: Dioecy, monoecy, gynodioecy, and an updated online database, American Journal of Botany, vol.101, pp.1588-1596, 2014.

S. S. Renner and R. E. Ricklefs, Dioecy and its correlates in the flowering plants, American Journal of Botany, vol.82, pp.596-606, 1995.

P. Saumitou-laprade, P. Vernet, C. Vassiliadis, Y. Hoareau, G. De-magny et al., A SelfIncompatibility System Explains High Male Frequencies in an Androdioecious Plant, Science, vol.327, pp.1648-1650, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00461836

S. Schultz, Nucleo-Cytoplasmic male sterility and alternative routes to dioecy, In: Evolution, vol.48, pp.1933-1945, 1994.

A. Sousa, S. S. Fuchs, and . Renner, Molecular Cytogenetics (FISH, GISH) of Coccinia grandis : A ca. 3 myrOld Species of Cucurbitaceae with the Largest Y/Autosome Divergence in Flowering Plants, Cytogenetic and genome research, 2012.

R. B. Spigler and T. L. Ashman, Gynodioecy to dioecy: are we there yet?, In: Ann. Bot, vol.109, issue.3, pp.531-543, 2012.

R. Taylor and D. R. , The genetic basis of sex ratio in Silene alba (= S. latifolia)". In: Genetics, vol.136, pp.641-651, 1994.

P. Touzet and E. H. Meyer, Cytoplasmic male sterility and mitochondrial metabolism in plants, p.19
URL : https://hal.archives-ouvertes.fr/hal-01110896

B. Pt, , pp.166-171, 2014.

R. Vanburen, Origin and domestication of papaya Y h chromosome, Genome Research, pp.524-533, 2015.

J. Wang, Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.13710-13715, 2012.

S. C. Weeks, The role of androdioecy and gynodioecy in mediating evolutionary transitions between dioecy and hermaphroditism in the animalia, Evolution 66, vol.12, pp.3670-3686, 2012.

J. Zluvova, M. Lengerova, M. Markova, R. Hobza, M. Nicolas et al., The inter-specific hybrid Silene latifolia x S. viscosa reveals early events of sex chromosome evolution, Evol. Dev, vol.7, pp.327-336, 2005.

J. Zluvova, S. Georgiev, B. Janousek, D. Charlesworth, B. Vyskot et al., Early events in the evolution of the Silene latifolia Y chromosome: Male specialization and recombination arrest, Genetics, vol.177, pp.375-386, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00412575

R. References-bergero and D. Charlesworth, Preservation of the Y transcriptome in a 10-millionyear-old plant sex chromosome system, Curr. Biol, vol.21, pp.1470-1474, 2011.

R. Bergero, D. Charlesworth, R. C. Filatov, and . Moore, Defining regions and rearrangements of the Silene latifolia Y chromosome, In: Genetics, vol.178, pp.2045-53, 2008.

G. Bernasconi, Silene as a model system in ecology and evolution, Heredity (Edinb), vol.103, pp.5-14, 2009.
DOI : 10.1038/hdy.2009.34

URL : https://hal.archives-ouvertes.fr/hal-00428347

A. Boualem, A conserved mutation in an ethylene biosynthesis enzyme leads to andromonoecy in melons, Science, vol.321, pp.836-844, 2008.

A. Boualem, A cucurbit androecy gene reveals how unisexual flowers develop and dioecy emerges, Science, vol.350, pp.688-691, 2015.
DOI : 10.1126/science.aac8370

URL : http://prodinra.inra.fr/ft/E368C59A-5C5B-4769-80ED-7A3C8D755C26

M. V. Chibalina and D. A. Filatov, Plant Y chromosome degeneration is retarded by haploid purifying selection, Curr. Biol, vol.21, pp.1475-1479, 2011.
DOI : 10.1016/j.cub.2011.07.045

URL : https://doi.org/10.1016/j.cub.2011.07.045

C. Fruchard and G. A. Marais, The Evolution of Sex Determination in Plants, Evolutionary Developmental Biology: A Reference Guide, pp.1-14, 2017.

A. G. Ghadge, K. Karmakar, R. S. Devani, J. Banerjee, B. Mohanasundaram et al., Flower development, pollen fertility and sex expression analyses of three sexual phenotypes of Coccinia grandis, BMC Plant Biology, vol.14, p.325, 2014.

Y. Kazama, A new physical mapping approach refines the sex-determining gene positions on the Silene latifolia Y-chromosome, In: Scientific Reports, vol.6, p.18917, 2016.

E. Kejnovsky, Z. Kubat, R. Hobza, M. Lengerova, S. Sato et al., Accumulation of chloroplast DNA sequences on the Y chromosome of Silene latifolia, Genetica, vol.128, issue.3, pp.167-175, 2006.

Z. Kubat, R. Hobza, B. Vyskot, and E. Kejnovsky, Microsatellite accumulation on the Y chromosome in Silene latifolia, Genome 51, vol.5, pp.350-356, 2008.

M. Lengerova, E. Kejnovsky, R. Hobza, J. Macas, S. R. Grant et al., Multicolor FISH mapping of the dioecious model plant, Silene latifolia, Theor. Appl. Genet, vol.108, pp.1193-1199, 2004.

A. Martin, C. Troadec, A. Boualem, M. Rajab, R. Fernandez et al., A transposon-induced epigenetic change leads to sex determination in melon, Nature, vol.461, pp.1135-1143, 2009.
DOI : 10.1038/nature08498

URL : https://hal.archives-ouvertes.fr/hal-01203855

A. Muyle, N. Zemp, C. Deschamps, S. Mousset, A. Widmer et al., Rapid de novo evolution of X chromosome dosage compensation in Silene latifolia, a plant with young sex chromosomes, PLoS Biol, vol.10, p.1001308, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698081

A. Muyle, . Käfer, . Zemp, . Mousset, G. A. Picard et al., SEX-DETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms, Genome Biology and Evolution, vol.8, pp.2530-2543, 2016.
DOI : 10.1093/gbe/evw172

URL : https://hal.archives-ouvertes.fr/hal-02053627

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.
DOI : 10.1073/pnas.1508454112

URL : http://www.pnas.org/content/112/42/13021.full.pdf

E. J. Pritham, Y. H. Zhang, C. Feschotte, and R. V. Kesseli, An Ac-like transposable element family with transcriptionally active Y-linked copies in the white campion, Silene latifolia, Genetics 165, vol.2, pp.799-807, 2003.

R. Roy and P. Roy, Ea-utils: 'Command-line tools for processing biological sequencing data', References Aronesty, E, vol.50, pp.391-400, 1971.

D. Bachtrog, The temporal dynamics of processes underlying Y chromosome degeneration, Genetics, vol.179, pp.1513-1525, 2008.

D. Bachtrog and B. Charlesworth, Reduced adaptation of a non-recombining neo-Y chromosome, Nature, vol.416, pp.323-326, 2002.

D. Bachtrog, Sex determination: why so many ways of doing it?, In: PLoS Biol, vol.12, p.1001899, 2014.

H. Badouin, The sunflower genome provides insights into oil metabolism, flowering and Asterid evolution, pp.148-152, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01603287

S. C. Barrett and J. Hough, Sexual dimorphism in flowering plants, J. Exp. Bot. 64, vol.1, pp.67-82, 2013.

F. E. Beaudry, S. C. Barrett, and S. I. Wright, Genomic Loss and Silencing on the Y Chromosomes of Rumex, Genome Biol Evol, vol.9, pp.3345-3355, 2017.

, Genome Biology and Evolution, vol.4, pp.740-749, 2012.

R. Vanburen, Origin and domestication of papaya Y h chromosome, Genome Research, pp.524-533, 2015.

R. A. Veitia, F. Veyrunes, S. Bottani, and J. A. Birchler, X chromosome inactivation and active X upregulation in therian mammals: facts, questions, and hypotheses, J Mol Cell Biol, vol.7, issue.1, pp.2-11, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01131346

J. Wang, Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.13710-13715, 2012.

Z. Yang, PAML 4: phylogenetic analysis by maximum likelihood, Mol. Biol. Evol, vol.24, pp.1586-1591, 2007.

M. D. Young, M. J. Wakefield, G. K. Smyth, A. Oshlack, ;. Zemp et al., Gene ontology analysis for RNA-seq: accounting for selection bias, Genome Biol, vol.11, issue.2, p.16168, 2010.

F. Zimmer, P. W. Harrison, C. Dessimoz, and J. E. Mank, Compensation of Dosage-Sensitive Genes on the Chicken Z Chromosome, Genome biology and evolution, vol.8, pp.1233-1242, 2016.

, References 75

R. Bergero and D. Charlesworth, Preservation of the Y transcriptome in a 10million-year-old plant sex chromosome system, Curr. Biol, vol.21, pp.1470-1474, 2011.

R. Bergero, D. Charlesworth, R. C. Filatov, and . Moore, Defining regions and rearrangements of the Silene latifolia Y chromosome, In: Genetics, vol.178, pp.2045-53, 2008.

G. Bernasconi, Silene as a model system in ecology and evolution, Heredity (Edinb), vol.103, pp.5-14, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00428347

N. Blavet, Identifying new sexlinked genes through BAC sequencing in the dioecious plant Silene latifolia, BMC Genomics, vol.16, issue.1, p.546, 2015.
URL : https://hal.archives-ouvertes.fr/hal-02044941

A. M. Bolger, M. Lohse, and B. Usadel, Trimmomatic: a flexible trimmer for Illumina sequence data, pp.2114-2120, 2014.

B. Buchfink, C. Xie, and D. H. Huson, Fast and sensitive protein alignment using DIAMOND, Nat. Methods, vol.12, pp.59-60, 2015.

C. Camacho, G. Coulouris, V. Avagyan, N. Ma, J. Papadopoulos et al., BLAST+: architecture and applications, In: BMC Bioinformatics, vol.10, p.421, 2009.

P. Capal, N. Blavet, J. Vrana, M. Kubalakova, and J. Dolezel, Multiple displacement amplification of the DNA from single flow-sorted plant chromosome, Plant Journal, vol.84, pp.838-844, 2015.

A. B. Carvalho and A. G. Clark, Efficient identification of Y chromosome sequences in the human and Drosophila genomes, Genome Res, vol.23, pp.1894-1907, 2013.

Y. C. Chen, T. Liu, C. H. Yu, T. Y. Chiang, C. C. Hwang-;-m et al., Effects of GC bias in next-generation-sequencing data on de novo genome assembly, PLoS ONE 8.4 (2013), e62856. Chibalina, vol.21, pp.1475-1479, 2011.

R. Chikhi and P. Medvedev, Informed and automated k-mer size selection for genome assembly, Bioinformatics, vol.30, pp.31-37, 2014.
DOI : 10.1093/bioinformatics/btt310

URL : https://hal.archives-ouvertes.fr/hal-01477511

A. Conesa, S. Gotz, J. M. Garcia-gomez, J. Terol, M. Talon et al., Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research, Bioinformatics, vol.21, pp.3674-3676, 2005.
DOI : 10.1093/bioinformatics/bti610

URL : https://academic.oup.com/bioinformatics/article-pdf/21/18/3674/521920/bti610.pdf

W. De-coster, D. T. S.-d'hert, M. Schultz, C. Cruts, and . Van-broeckhoven, NanoPack: visualizing and processing long read sequencing data, Bioinformatics, 2018.

M. Deutsch and M. Long, Intron-exon structures of eukaryotic model organisms, Nucleic Acids Res, vol.27, pp.3219-3228, 1999.

A. C. English, Mind the Gap: Upgrading Genomes with Pacific Biosciences RS Long-Read Sequencing Technology, PLoS ONE, vol.7, issue.11, pp.1-12, 2012.
DOI : 10.1371/journal.pone.0047768

URL : https://doi.org/10.1371/journal.pone.0047768

A. B. Hall, Radical remodeling of the Y chromosome in a recent radiation of malaria mosquitoes, Proceedings of the National Academy of Sciences, vol.113, p.201525164, 2016.

J. F. Hughes and S. Rozen, Genomics and genetics of human and primate y chromosomes, Annu Rev Genomics Hum Genet, vol.13, pp.83-108, 2012.
DOI : 10.1146/annurev-genom-090711-163855

J. F. Hughes, Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content, Nature, vol.463, pp.536-539, 2010.
DOI : 10.1038/nature08700

URL : http://europepmc.org/articles/pmc3653425?pdf=render

J. F. Hughes, Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes, Nature, vol.483, pp.82-86, 2012.
DOI : 10.1038/nature10843

URL : http://europepmc.org/articles/pmc3292678?pdf=render

C. L. Ip, MinION Analysis and Reference Consortium: Phase 1 data release and analysis, p.1000, 2015.
DOI : 10.12688/f1000research.7201.1

URL : https://f1000research.com/articles/4-1075/v1/pdf

Y. Kazama, A new physical mapping approach refines the sex-determining gene positions on the Silene latifolia Ychromosome, In: Scientific Reports, vol.6, pp.656-664, 2002.
DOI : 10.1038/srep18917

URL : http://www.nature.com/articles/srep18917.pdf

F. J. Krsticevic, C. G. Schrago, and A. B. Carvalho, Long-Read Single Molecule Sequencing to Resolve Tandem Gene Copies: The Mst77Y Region on the Drosophila melanogaster Y Chromosome, p.3
DOI : 10.1534/g3.115.017277

URL : http://www.g3journal.org/content/ggg/5/6/1145.full.pdf

, Genes|Genomes|Genetics, vol.5, pp.1145-1150, 2015.

S. Kumar, M. Jones, G. Koutsovoulos, M. Clarke, and M. Blaxter, Blobology: exploring raw genome data for contaminants, symbionts and parasites using taxon-annotated GC-coverage plots, In: Front Genet, vol.4, p.237, 2013.
DOI : 10.3389/fgene.2013.00237

URL : https://www.frontiersin.org/articles/10.3389/fgene.2013.00237/pdf

R. S. Lasken and T. B. Stockwell, Mechanism of chimera formation during the Multiple Displacement Amplification reaction, BMC Biotechnol, vol.7, p.19, 2007.

T. Laver, J. Harrison, P. A. O'neill, K. Moore, A. Farbos et al., Assessing the performance of the Oxford Nanopore Technologies MinION, Biomolecular Detection and Quantification, vol.3, pp.1-8, 2015.

C. Li, F. Lin, D. An, W. Wang, and R. Huang, Genome Sequencing and Assembly by Long Reads in Plants, Genes (Basel), vol.9, p.1, 2017.

N. J. Loman, J. Quick, and J. T. Simpson, A complete bacterial genome assembled de novo using only nanopore sequencing data, Nature Methods, vol.12, pp.733-735, 2015.
DOI : 10.1101/015552

URL : https://www.biorxiv.org/content/early/2015/03/11/015552.full.pdf

H. Lu, F. Giordano, and Z. Ning, Oxford Nanopore MinION Sequencing and Genome Assembly, Genomics, Proteomics and Bioinformatics, vol.14, pp.265-279, 2016.

J. Macas, E. Kejnovský, P. Neumann, P. Novák, A. Koblí?ková et al., Next generation sequencing-based analysis of repetitive DNA in the model dioceous plant silene latifolia, PLoS ONE, vol.6, p.11, 2011.

K. Murase, MYB transcription factor gene involved in sex determination in Asparagus officinalis, Genes to Cells, vol.22, pp.115-123, 2017.

A. Muyle, N. Zemp, C. Deschamps, S. Mousset, A. Widmer et al., Rapid de novo evolution of X chromosome dosage compensation in Silene latifolia, a plant with young sex chromosomes, PLoS Biol, vol.10, p.1001308, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698081

A. Muyle, . Käfer, . Zemp, . Mousset, G. A. Picard et al., SEXDETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms, Genome Biology and Evolution, vol.8, pp.2530-2543, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02053627

A. Muyle, G. A. Shearn, and . Marais, The Evolution of Sex Chromosomes and Dosage Compensation in Plants, Genome Biology and Evolution, vol.9, pp.627-645, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01943816

S. P. Otto, About PAR: the distinct evolutionary dynamics of the pseudoautosomal region, Trends Genet, vol.27, pp.358-367, 2011.

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.

S. Rangavittal, R. S. Harris, M. Cechova, M. Tomaszkiewicz, R. Chikhi et al., RecoverY: k-mer-based read classification for Ychromosome-specific sequencing and assembly, Bioinformatics, vol.34, pp.1125-1131, 2018.

A. Rhoads and K. F. Au, PacBio Sequencing and Its Applications, Genomics, vol.13, pp.278-289, 2015.

E. Sallet, J. Gouzy, and T. Schiex, EuGene-PP: a next-generation automated annotation pipeline for prokaryotic genomes, Bioinformatics, vol.30, pp.2659-2661, 2014.

L. Salmela and E. Rivals, LoRDEC: Accurate and efficient long read error correction, Bioinformatics, vol.30, pp.3506-3514, 2014.
URL : https://hal.archives-ouvertes.fr/lirmm-01100451

R. Schmieder and R. Edwards, Quality control and preprocessing of metagenomic datasets, Bioinformatics, vol.27, pp.863-864, 2011.

H. Skaletsky, The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes, Nature, vol.423, pp.825-837, 2003.

Y. Q. Soh, Sequencing the mouse y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes, In: Cell, vol.159, pp.800-813, 2014.

J. I. Sohn and J. W. Nam, The present and future of de novo whole-genome assembly, Brief. Bioinformatics, vol.19, issue.1, pp.23-40, 2018.

J. A. Tennessen, N. Wei, S. Straub, R. Govindarajulu, A. Liston et al.,

. Ashman, Repeated translocation of a gene cassette drives sex chromosome turnover in strawberries, p.bioRxiv, 2017.

M. Tomaszkiewicz, A time-and cost-effective strategy to sequence mammalian Y chromosomes: An application to the de novo assembly of gorilla Y, Genome Research, vol.26, pp.530-540, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01395702

B. Vicoso and D. Bachtrog, Reversal of an ancient sex chromosome to an autosome in Drosophila, Nature, vol.499, pp.332-335, 2013.

J. Vrana, P. Capal, H. Simkova, M. Karafiatova, J. Cizkova et al., Flow Analysis and Sorting of Plant Chromosomes, Curr Protoc Cytom, vol.78, pp.1-5, 2016.

J. Wang, Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.13710-13715, 2012.

R. Wick, Porechop: adapter trimmer for Oxford Nanopore reads, Available online at github.com/rwick/Porechop, 2017.

T. D. Wu and C. K. Watanabe, GMAP: a genomic mapping and alignment program for mRNA and EST sequences, Bioinformatics, vol.21, pp.1859-1875, 2005.

W. Xue, J. Li, Y. Zhu, G. Hou, X. Kong et al., L_RNA_scaffolder: scaffolding genomes with transcripts, In: BMC genomics, vol.14, issue.1, p.604, 2013.
DOI : 10.1186/1471-2164-14-604

URL : https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/1471-2164-14-604

C. Ye, C. M. Hill, S. Wu, J. Ruan, and Z. S. Ma, DBG2OLC: Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies, In: Sci Rep, vol.6, p.31900, 2016.

N. Zemp, R. Tavares, A. Muyle, D. Charlesworth, G. A. Marais et al., Evolution of sex-biased gene expression in a dioecious plant, Nature Plants, vol.2, p.16168, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02049902

A. V. Zimin, G. Marcais, D. Puiu, M. Roberts, S. L. Salzberg et al., The MaSuRCA genome assembler, Bioinformatics, vol.29, pp.2669-2677, 2013.
DOI : 10.1093/bioinformatics/btt476

URL : https://academic.oup.com/bioinformatics/article-pdf/29/21/2669/18533361/btt476.pdf

T. Akagi, I. M. Henry, R. Tao, and L. Comai, A Y-chromosome-encoded small RNA acts as a sex determinant in persimmons, Science, vol.346, pp.646-650, 2014.

T. L. Ashman, J. A. Tennessen, R. M. Dalton, R. Govindarajulu, M. H. Koski et al., Multilocus Sex Determination Revealed in Two Populations of Gynodioecious Wild Strawberry, Fragaria vesca subsp. bracteata, G3 (Bethesda), vol.5, pp.2759-2773, 2015.

N. Blavet, Identifying new sex-linked genes through BAC sequencing in the dioecious plant Silene latifolia, BMC Genomics, vol.16, issue.1, p.546, 2015.
URL : https://hal.archives-ouvertes.fr/hal-02044941

A. Boualem, A cucurbit androecy gene reveals how unisexual flowers develop and dioecy emerges, Science, vol.350, pp.688-691, 2015.

J. Dahan and H. Mireau, The Rf and Rf-like PPR in higher plants, a fast-evolving subclass of PPR genes, In: RNA biology, vol.10, pp.1469-1476, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01204003

R. S. Devani, S. Sinha, J. Banerjee, R. K. Sinha, A. Bendahmane et al., De novo transcriptome assembly from flower buds of dioecious, gynomonoecious and chemically masculinized female Coccinia grandis reveals genes associated with sex expression and modification, BMC Plant Biol, vol.17, p.241, 2017.

S. R. Eddy, Profile hidden Markov models, Bioinformatics, vol.14, pp.755-763, 1998.

C. Fruchard and G. A. Marais, The Evolution of Sex Determination in Plants, Evolutionary Developmental Biology: A Reference Guide, pp.1-14, 2017.

W. Huang, Pentatricopeptide-repeat family protein RF6 functions with hexokinase 6 to rescue rice cytoplasmic male sterility, Proc. Natl. Acad. Sci. U.S.A, vol.112, pp.14984-14989, 2015.

A. Martin, C. Troadec, A. Boualem, M. Rajab, R. Fernandez et al., A transposon-induced epigenetic change leads to sex determination in melon, Nature, vol.461, pp.1135-1143, 2009.
URL : https://hal.archives-ouvertes.fr/hal-01203855

J. N. Mohanty, S. Nayak, S. Jha, and R. K. Joshi, Transcriptome profiling of the floral buds and discovery of genes related to sex-differentiation in the dioecious cucurbit Coccinia grandis (L.) Voigt, Gene, vol.626, pp.395-406, 2017.

A. Muyle, . Käfer, . Zemp, . Mousset, G. A. Picard et al., SEX-DETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms, Genome Biology and Evolution, vol.8, pp.2530-2543, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02053627

A. Muyle, G. A. Shearn, and . Marais, The Evolution of Sex Chromosomes and Dosage Compensation in Plants, Genome Biology and Evolution, vol.9, pp.627-645, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01943816

A. Muyle, Genomic imprinting mediates dosage compensation in a young plant XY system, p.bioRxiv, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01851376

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.

M. Tomaszkiewicz, P. Medvedev, and K. D. Makova, Y and W Chromosome Assemblies: Approaches and Discoveries, Trends in Genetics, vol.33, pp.266-282, 2017.

T. D. Wu and C. K. Watanabe, GMAP: a genomic mapping and alignment program for mRNA and EST sequences, Bioinformatics, vol.21, pp.1859-1875, 2005.

S. E. Albritton, A. L. Kranz, P. Rao, M. Kramer, C. Dieterich et al., Sex-biased gene expression and evolution of the x chromosome in nematodes, Genetics, vol.197, pp.865-883, 2014.

D. Bachtrog, Y-chromosome evolution: emerging insights into processes of Ychromosome degeneration, Nat. Rev. Genet, vol.14, pp.113-124, 2013.

R. Bergero and D. Charlesworth, Preservation of the Y transcriptome in a 10million-year-old plant sex chromosome system, Curr. Biol, vol.21, pp.1470-1474, 2011.

R. Bergero, S. Qiu, and D. Charlesworth, Gene loss from a plant sex chromosome system, Current Biology, vol.25, pp.1234-1240, 2015.

B. Charlesworth, The evolution of chromosomal sex determination and dosage compensation, Curr. Biol, vol.6, pp.149-162, 1996.

M. V. Chibalina and D. A. Filatov, Plant Y chromosome degeneration is retarded by haploid purifying selection, Curr. Biol, vol.21, pp.1475-1479, 2011.

C. Disteche, Dosage compensation of the sex chromosomes, Annu. Rev. Genet, vol.46, pp.537-560, 2012.

H. Ellegren and J. Parsch, The evolution of sex-biased genes and sex-biased gene expression, In: Nature reviews. Genetics, vol.8, issue.9, pp.689-98, 2007.

S. Ercan, Mechanisms of x chromosome dosage compensation, J Genomics, vol.3, pp.1-19, 2015.

L. Gu and J. R. Walters, Evolution of Sex Chromosome Dosage Compensation in Animals: A Beautiful Theory, Undermined by Facts and Bedeviled by Details, Genome Biol Evol, vol.9, pp.2461-2476, 2017.

P. Julien, D. Brawand, M. Soumillon, A. Necsulea, A. Liechti et al., Mechanisms and evolutionary patterns of mammalian and avian dosage compensation, PLoS Biol, vol.10, pp.1269-1278, 2012.

M. I. Kuroda, A. Hilfiker, and J. C. Lucchesi, Dosage Compensation in Drosophila-a Model for the Coordinate Regulation of Transcription, Genetics, vol.204, pp.435-450, 2016.

J. H. Malone, Mediation of Drosophila autosomal dosage effects and compensation by network interactions, Genome Biol, vol.13, p.28, 2012.

J. E. Mank, Sex chromosome dosage compensation: definitely not for everyone, Trends Genet. 29, vol.12, pp.677-683, 2013.

A. Muyle, N. Zemp, C. Deschamps, S. Mousset, A. Widmer et al., Rapid de novo evolution of X chromosome dosage compensation in Silene latifolia, a plant with young sex chromosomes, PLoS Biol, vol.10, p.1001308, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698081

A. Muyle, . Käfer, . Zemp, . Mousset, G. A. Picard et al., SEXDETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms, Genome Biology and Evolution, vol.8, pp.2530-2543, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02053627

A. Muyle, G. A. Shearn, and . Marais, The Evolution of Sex Chromosomes and Dosage Compensation in Plants, Genome Biology and Evolution, vol.9, pp.627-645, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01943816

S. Ohno, Sex Chromosomes and Sex-Linked Genes, p.192, 1967.

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.

M. M. Patten, L. Ross, J. P. Curley, D. C. Queller, R. Bonduriansky et al., The evolution of genomic imprinting: theories, predictions and empirical tests, Heredity (Edinb), vol.113, pp.119-128, 2014.

E. Pessia, T. Makino, M. Bailly-bechet, A. Mclysaght, and G. A. Marais, Mammalian X chromosome inactivation evolved as a dosage-compensation mechanism for dosage-sensitive genes on the X chromosome, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.5346-5351, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698392

E. Pessia, J. Engelstadter, and G. A. Marais, The evolution of X chromosome inactivation in mammals: the demise of Ohno's hypothesis?, In: Cell

. Mol, Life Sci, vol.71, pp.1383-1394, 2014.

A. Rautenberg, L. Hathaway, B. Oxelman, and H. C. Prentice, Geographic and phylogenetic patterns in Silene section Melandrium (Caryophyllaceae) as inferred from chloroplast and nuclear DNA sequences, Mol. Phylogenet. Evol, vol.57, pp.978-991, 2010.

J. Siroky, M. R. Castiglione, and B. Vyskot, DNA methylation patterns of Melandrium album chromosomes, Chromosome Res, vol.6, pp.441-446, 1998.

R. A. Veitia, F. Veyrunes, S. Bottani, and J. A. Birchler, X chromosome inactivation and active X upregulation in therian mammals: facts, questions, and hypotheses, J Mol Cell Biol, vol.7, issue.1, pp.2-11, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01131346

A. Wagschal and R. Feil, Genomic imprinting in the placenta
URL : https://hal.archives-ouvertes.fr/hal-02262474

, Genome Res, vol.113, issue.4, pp.90-98, 2006.

D. J. Whitworth and A. J. Pask, The X factor: X chromosome dosage compensation in the evolutionarily divergent monotremes and marsupials, In: Semin. Cell Dev. Biol, vol.56, pp.117-121, 2016.

T. D. Wu and S. Nacu, Fast and SNPtolerant detection of complex variants and splicing in short reads, Bioinformatics, vol.26, pp.873-881, 2010.

N. Zemp, R. Tavares, A. Muyle, D. Charlesworth, G. A. Marais et al., Ea-utils: 'Command-line tools for processing biological sequencing data', Nature Plants, vol.2, pp.403-410, 1990.

I. Atanassov, C. Delichere, D. A. Filatov, D. Charlesworth, I. Negrutiu et al., Analysis and evolution of two functional Ylinked loci in a plant sex chromosome system, Mol. Biol. Evol. 18, vol.12, pp.2162-2168, 2001.

R. Bergero, A. Forrest, E. Kamau, and D. Charlesworth, Evolutionary strata on the X chromosomes of the dioecious plant Silene latifolia: evidence from new sex-linked genes, Genetics, vol.175, pp.1945-1954, 2007.

R. Bergero, S. Qiu, A. Forrest, H. Borthwick, and D. Charlesworth, Expansion of the pseudoautosomal region and ongoing recombination suppression in the Silene latifolia sex chromosomes, Genetics, vol.194, pp.673-686, 2013.

R. Bergero, S. Qiu, and D. Charlesworth, Gene loss from a plant sex chromosome system, Current Biology, vol.25, pp.1234-1240, 2015.

N. Blavet, Identifying new sex-linked genes through BAC sequencing in the dioecious plant Silene latifolia, BMC Genomics, vol.16, issue.1, p.546, 2015.
URL : https://hal.archives-ouvertes.fr/hal-02044941

R. Cegan, G. A. Marais, H. Kubekova, N. Blavet, A. Widmer et al., Structure and evolution of Apetala3, a sex-linked gene in Silene latifolia, In: BMC plant biology, vol.10, p.180, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00539504

M. V. Chibalina and D. A. Filatov, Plant Y chromosome degeneration is retarded by haploid purifying selection, Curr. Biol, vol.21, pp.1475-1479, 2011.
DOI : 10.1016/j.cub.2011.07.045

URL : https://doi.org/10.1016/j.cub.2011.07.045

R. Chikhi and P. Medvedev, Informed and automated k-mer size selection for genome assembly, Bioinformatics, vol.30, pp.31-37, 2014.
DOI : 10.1093/bioinformatics/btt310

URL : https://hal.archives-ouvertes.fr/hal-01477511

A. Conesa, S. Gotz, J. M. Garcia-gomez, J. Terol, M. Talon et al., Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research, Bioinformatics, vol.21, pp.3674-3676, 2005.

C. Delichere, J. Veuskens, M. Hernould, N. Barbacar, A. Mouras et al., SlY1, the first active gene cloned from a plant Y chromosome, encodes a WD-repeat protein, EMBO J, vol.18, pp.4169-4179, 1999.

M. A. Depristo, A framework for variation discovery and genotyping using nextgeneration DNA sequencing data

, Genet. 43, vol.5, pp.491-498, 2011.

D. A. Filatov, Evolutionary history of Silene latifolia sex chromosomes revealed by genetic mapping of four genes, Genetics, vol.170, pp.975-979, 2005.

P. Gayral, Reference-free population genomics from next-generation transcriptome data and the vertebrate-invertebrate gap, In: PLoS genetics, vol.9, p.1003457, 2013.
URL : https://hal.archives-ouvertes.fr/hal-00866204

R. Hobza and A. Widmer, Efficient molecular sexing in dioecious Silene latifolia and S. dioica and paternity analysis in F(1) hybrids, Mol Ecol Resour, vol.8, pp.1274-1276, 2008.

C. Jenkins and S. R. Keller, A phylogenetic comparative study of preadaptation for invasiveness in the genus Silene (Caryophyllaceae), Biological Invasions, vol.13, pp.1471-1486, 2011.

V. B. Kaiser, R. Bergero, and D. Charlesworth, A new plant sex-linked gene with high sequence diversity and possible introgression of the X copy, Heredity (Edinb), vol.106, pp.339-347, 2011.

Y. Kazama, K. Nishihara, R. Bergero, M. T. Fujiwara, T. Abe et al., SlWUS1; an X-linked gene having no homologous Y-linked copy in Silene latifolia, G3 (Bethesda), vol.2, pp.1269-1278, 2012.

H. Li and R. Durbin, Fast and accurate short read alignment with Burrows-Wheeler transform, Bioinformatics, vol.25, pp.1754-1760, 2009.
DOI : 10.1093/bioinformatics/btp324

URL : https://academic.oup.com/bioinformatics/article-pdf/25/14/1754/605544/btp324.pdf

H. Li, B. Handsaker, A. Wysoker, T. Fennell, J. Ruan et al., The Sequence Alignment/Map format and SAMtools, Bioinformatics, vol.25, pp.2078-2079, 2009.

R. Luo, SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler, In: Gigascience, vol.1, issue.1, p.18, 2012.

S. Matsunaga, S. Lebel-hardenack, E. Kejnovsky, B. Vyskot, S. R. Grant et al., An anther-and petal-specific gene SlMF1 is a multicopy gene with homologous sequences on sex chromosomes, Genes Genet. Syst, vol.80, pp.395-401, 2005.

S. Matsunaga, S. Kawano, H. Takano, H. Uchida, A. Sakai et al., Isolation and developmental expression of male reproductive organ-specific genes in a dioecious campion, Melandrium album (Silene latifolia), In: Plant J, vol.10, pp.679-689, 1996.

R. C. Moore, O. Kozyreva, S. Lebel-hardenack, J. Siroky, R. Hobza et al., Genetic and functional analysis of DD44, a sex-linked gene from the dioecious plant Silene latifolia, provides clues to early events in sex chromosome evolution, Genetics, vol.163, pp.321-334, 2003.

A. Muyle, N. Zemp, C. Deschamps, S. Mousset, A. Widmer et al., Rapid de novo evolution of X chromosome dosage compensation in Silene latifolia, a plant with young sex chromosomes, PLoS Biol, vol.10, p.1001308, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698081

A. Muyle, . Käfer, . Zemp, . Mousset, G. A. Picard et al., SEX-DETector: A Probabilistic Approach to Study Sex Chromosomes in Non-Model Organisms, Genome Biology and Evolution, vol.8, pp.2530-2543, 2016.
DOI : 10.1093/gbe/evw172

URL : https://hal.archives-ouvertes.fr/hal-02053627

A. Muyle, G. A. Shearn, and . Marais, The Evolution of Sex Chromosomes and Dosage Compensation in Plants, Genome Biology and Evolution, vol.9, pp.627-645, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01943816

A. Oshlack, M. D. Robinson, and M. D. Young, From RNA-seq reads to differential expression results, Genome Biol. 11, vol.12, p.220, 2010.
DOI : 10.1186/gb-2010-11-12-220

URL : https://genomebiology.biomedcentral.com/track/pdf/10.1186/gb-2010-11-12-220

A. S. Papadopulos, M. Chester, K. Ridout, and D. A. Filatov, Rapid Y degeneration and dosage compensation in plant sex chromosomes, Proceedings of the National Academy of Sciences, vol.112, pp.13021-13026, 2015.
DOI : 10.1073/pnas.1508454112

URL : http://www.pnas.org/content/112/42/13021.full.pdf

E. Pessia, T. Makino, M. Bailly-bechet, A. Mclysaght, and G. A. Marais, Mammalian X chromosome inactivation evolved as a dosagecompensation mechanism for dosage-sensitive genes on the X chromosome, Proc. Natl. Acad. Sci. U.S.A, vol.109, pp.5346-5351, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00698392

S. Qiu, R. Bergero, K. Zeng, and D. Charlesworth, Patterns of codon usage bias in Silene latifolia, Mol. Biol. Evol, vol.28, issue.1, pp.771-780, 2011.

P. Rastas, L. Paulin, I. Hanski, R. Lehtonen, and P. Auvinen, Lep-MAP: fast and accurate linkage map construction for large SNP datasets, Bioinformatics, vol.29, pp.3128-3134, 2013.
DOI : 10.1093/bioinformatics/btt563

URL : https://academic.oup.com/bioinformatics/article-pdf/29/24/3128/25024839/btt563.pdf

A. Rautenberg, L. Hathaway, B. Oxelman, and H. C. Prentice, Geographic and phylogenetic patterns in Silene section Melandrium (Caryophyllaceae) as inferred from chloroplast and nuclear DNA sequences, In: Mol. Phylogenet. Evol, vol.57, pp.978-991, 2010.
DOI : 10.1016/j.ympev.2010.08.003

A. Rautenberg, D. B. Sloan, V. Aldén, and B. Oxelman, Phylogenetic Relationships of Silene multinervia and Silene Section Conoimorpha (Caryophyllaceae), Systematic Botany, vol.37, pp.226-237, 2012.

M. D. Robinson, D. J. Mccarthy, and G. K. Smyth, edgeR: a Bioconductor package for differential expression analysis of digital gene expression data, Bioinformatics, vol.26, pp.139-140, 2010.

J. Siroky, M. R. Castiglione, and B. Vyskot, DNA methylation patterns of Melandrium album chromosomes, Chromosome Res, vol.6, pp.441-446, 1998.

G. Tsagkogeorga, V. Cahais, and N. Galtier, The population genomics of a fast evolver: High levels of diversity, functional constraint, andmolecular adaptation in the tunicate Ciona intestinalis, Genome Biology and Evolution, vol.4, pp.740-749, 2012.

J. W. Van-ooijen, Multipoint maximum likelihood mapping in a full-sib family of an outbreeding species, Genet Res (Camb), vol.93, pp.343-349, 2011.

J. Vrana, H. Simkova, M. Kubalakova, J. Cihalikova, and J. Dolezel, Flow cytometric chromosome sorting in plants: the next generation, In: Methods, vol.57, pp.331-337, 2012.

T. D. Wu and S. Nacu, Fast and SNP-tolerant detection of complex variants and splicing in short reads, Bioinformatics, vol.26, pp.873-881, 2010.

W. Xue, J. Li, Y. Zhu, G. Hou, X. F. Kong et al., L_RNA_scaffolder: scaffolding genomes with transcripts, BMC genomics, vol.14, issue.1, p.604, 2013.
DOI : 10.1186/1471-2164-14-604

URL : https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/1471-2164-14-604

N. Zemp, A. Minder, and A. Widmer, Identification of internal reference genes for gene expression normalization between the two sexes in dioecious white Campion, PLoS ONE, vol.9, p.92893, 2014.

N. Zemp, R. Tavares, A. Muyle, D. Charlesworth, G. A. Marais et al., Evolution of sex-biased gene expression in a dioecious plant, Nature Plants, vol.2, issue.11, p.16168, 2016.
URL : https://hal.archives-ouvertes.fr/hal-02049902

S. Figures,

, Ages at the nodes are shown in million years (My). The exact relationship among species is poorly resolved, Supplementary Figures and Tables Supplementary Figure B.S1, 2010.

. Rautenberg, References Supplementary Figure B.S2. Normalised difference in allelic expression levels between S. latifolia and the two outgroups without sex chromosomes S. vulgaris and S. viscosa (hereafter ?), in autosomal and sex-linked contigs in the seedling tissue. Maternal and paternal allelic read numbers were summed at SNP positions and normalised for each individual separately, then averaged among individuals for each contig. ? was computed as follows: ? =(allelic expression in S. latifolia ? allelic expression in the outgroup) / allelic expression in the outgroup). If ? is lower, higher or equal to zero, then expression in S. latifolia is respectively lower, higher or equal to the outgroup. For all contig categories, ? was compared to zero using a Wilcoxon test. The median ?, confidence intervals and p-values adjusted for, some phylogenies S. viscosa is closest to S. latifolia, whereas in others S. vulgaris is closest as shown here, and in others both species are equally diverged to S. latifolia, 2010.

*. , The Y/X ratio was computed in S. latifolia males and averaged among individuals to use as a proxy for Y degeneration. X-hemizygous contigs have a Y/X ratio equal to zero. Contigs with sex-biased expression were removed, as well as contigs with Y/X expression ratios above 1.5. Sample sizes for the different contig categories are, p.160

, Results show that the maternal allele is hyper-expressed in S. latifolia when the Y chromosome is degenerated, both in males and females. Supplementary Figure B.S3. Normalised difference in allelic expression levels between S.latifolia and the two outgroups without sex chromosomes S. vulgaris and S. viscosa (?), in autosomal and sex-linked contigs in the flower bud tissue. Same legend as Supplementary Figure B.S2 except for sample sizes for the different contig categories, autosomal contigs were randomly selected in order to have similar statistical power among gene categories)

, Supplementary Figure B.S6. Normalised difference in allelic expression levels between S.latifolia and the two outgroups without sex chromosomes S. vulgaris and S. viscosa (?), in autosomal and sex-linked contigs that were validated (see Materials and Methods section 2.5), for the flower bud tissue. Same legend as Supplementary Figure B.S2 except for sample sizes for the different contig categories