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Sex chromosome evolution among amniotes: is the origin of sex chromosomes non-random?

Kratochvíl, Lukáš, Gamble, Tony, Rovatsos, Michail·2021·Philosophical Transactions of the Royal Society B
DOI 10.1098/rstb.2020.0108
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Abstract

Sex chromosomes are a great example of a convergent evolution at the genomic level, having evolved dozens of times just within amniotes. An intriguing question is whether this repeated evolution was random, or whether some ancestral syntenic blocks have significantly higher chance to be co-opted for the role of sex chromosomes owing to their gene content related to gonad development. Here, we summarize current knowledge on the evolutionary history of sex determination and sex chromosomes in amniotes and evaluate the hypothesis of non-random emergence of sex chromosomes. The current data on the origin of sex chromosomes in amniotes suggest that their evolution is indeed non-random. However, this non-random pattern is not very strong, and many syntenic blocks representing putatively independently evolved sex chromosomes are unique. Still, repeatedly co-opted chromosomes are an excellent model system, as independent co-option of the same genomic region for the role of sex chromosome offers a great opportunity for testing evolutionary scenarios on the sex chromosome evolution under the explicit control for the genomic background and gene identity. Future studies should use these systems more to explore the convergent/divergent evolution of sex chromosomes. This article is part of the theme issue ‘Challenging the paradigm in sex chromosome evolution: empirical and theoretical insights with a focus on vertebrates (Part II)’.

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Research works printed but not linked: 125

  1. Bull, 1983, Evolution of sex determining mechanisms
  2. Capel, 2019, Sex determination in vertebrates
  3. Straková, 2020, Evolution of sex determination in amniotes: did stress and sequential hermaphroditism produce environmental determination?, BioEssays, 42, e2000050, 10.1002/bies.202000050 · DOI
  4. Ohno, 1967, Sex chromosomes and sex-linked Genes, 10.1007/978-3-642-88178-7 · DOI
  5. Charlesworth, 2005, Steps in the evolution of heteromorphic sex chromosomes, Heredity, 95, 118, 10.1038/sj.hdy.6800697 · DOI
  6. Fisher, 1931, The evolution of dominance, Biol. Rev., 6, 345, 10.1111/j.1469-185X.1931.tb01030.x · DOI
  7. Rice, 1984, Sex chromosomes and the evolution of sexual dimorphism, Evolution, 38, 735, 10.1111/j.1558-5646.1984.tb00346.x · DOI
  8. Furman, 2020, Sex chromosome evolution: so many exceptions to the rules, Genome Biol. Evol., 12, 750, 10.1093/gbe/evaa081 · DOI
  9. Myosho, 2015, Turnover of sex chromosomes in celebensis group Medaka fishes, G3: Genes Genom. Genet., 5, 2685, 10.1534/g3.115.021543 · DOI
  10. Jeffries, 2018, A rapid rate of sex-chromosome turnover and non-random transitions in true frogs, Nat. Commun., 9, 4088, 10.1038/s41467-018-06517-2 · DOI
  11. Lichilín, 2021, Sex-biased gene expression and recent sex chromosome turnover, Phil. Trans. R. Soc. B, 376, 20200107, 10.1098/rstb.2020.0107 · DOI
  12. Kostmann, 2021, Poorly differentiated XX/XY sex chromosomes are widely shared across skink radiation, Proc. R. Soc. B, 288, 20202139, 10.1098/rspb.2020.2139 · DOI
  13. Kuhl, 2021, A 180 Myr-old female-specific genome region in sturgeon reveals the oldest known vertebrate sex determining system with undifferentiated sex chromosomes, Phil. Trans. R. Soc. B, 376, 20200089, 10.1098/rstb.2020.0089 · DOI
  14. Graves, 2010, Are homologies in vertebrate sex determination due to shared ancestry or to limited options?, Genome Biol., 11, 205, 10.1186/gb-2010-11-4-205 · DOI
  15. Graves, 2009, Weird animal genomes and the evolution of vertebrate sex and sex chromosomes, Annu. Rev. Genet., 42, 565, 10.1146/annurev.genet.42.110807.091714 · DOI
  16. O'Meally, 2010, Non-homologous sex chromosomes of birds and snakes share repetitive sequences, Chromosome Res., 18, 787, 10.1007/s10577-010-9152-9 · DOI
  17. O'Meally, 2012, Are some chromosomes particularly good at sex? Insights from amniotes, Chromosome Res., 20, 7, 10.1007/s10577-011-9266-8 · DOI
  18. Livernois, 2012, The origin and evolution of vertebrate sex chromosomes and dosage compensation, Heredity, 108, 50, 10.1038/hdy.2011.106 · DOI
  19. Ezaz, 2017, Origin of amniote sex chromosomes: an ancestral super-sex chromosome, or common requirements?, J. Heredity, 108, 94, 10.1093/jhered/esw053 · DOI
  20. Rovatsos, 2019, The rise and fall of differentiated sex chromosomes in geckos, Mol. Ecol., 28, 3042, 10.1111/mec.15126 · DOI
  21. Cortez, 2014, Origins and functional evolution of Y chromosomes across mammals, Nature, 508, 488, 10.1038/nature13151 · DOI
  22. Zhou, 2014, Complex evolutionary trajectories of sex chromosomes across bird taxa, Science, 346, 1246338, 10.1126/science.1246338 · DOI · Paper page
  23. Sarre, 2004, The ends of a continuum: genetic and temperature-dependent sex determination in reptiles, BioEssays, 26, 639, 10.1002/bies.20050 · DOI
  24. Grossen, 2011, Temperature-dependent turnovers in sex-determination mechanisms: a quantitative model, Evolution, 65, 64, 10.1111/j.1558-5646.2010.01098.x · DOI
  25. Kumar, 2017, TimeTree: a resource for timelines, timetrees, and divergence times, Mol. Biol. Evol., 34, 1812, 10.1093/molbev/msx116 · DOI
  26. Shen, 2011, Multiple genome alignments facilitate development of NPCL markers: a case study of tetrapod phylogeny focusing on the position of turtles, Mol. Biol. Evol., 28, 3237, 10.1093/molbev/msr148 · DOI
  27. Pyron, 2013, A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes, BMC Evol. Biol., 13, 93, 10.1186/1471-2148-13-93 · DOI
  28. Nielsen, 2019, Escaping the evolutionary trap? Sex chromosome turnover in basilisks and related lizards (Corytophanidae: Squamata), Biol. Lett., 15, 20190498, 10.1098/rsbl.2019.0498 · DOI
  29. Rovatsos, 2015, Female heterogamety in Madagascar chameleons (Squamata: Chamaeleonidae: Furcifer): differentiation of sex and neo-sex chromosomes, Sci. Rep., 5, 13196, 10.1038/srep13196 · DOI
  30. Rovatsos, 2019, Little evidence for switches to environmental sex determination and turnover of sex chromosomes in lacertid lizards, Sci. Rep., 9, 7832, 10.1038/s41598-019-44192-5 · DOI
  31. Telemeco, 2015, Sex determination in southern alligator lizards (Elgaria multicarinata; Anguidae), Herpetologica, 71, 8, 10.1655/Herpetologica-D-14-00033 · DOI
  32. Nielsen, 2018, Dynamic sex chromosomes in Old World chameleons (Squamata: Chamaeleonidae), J. Evol. Biol., 31, 484, 10.1111/jeb.13242 · DOI
  33. Iannucci, 2019, Conserved sex chromosomes and karyotype evolution in monitor lizards (Varanidae), Heredity, 123, 215, 10.1038/s41437-018-0179-6 · DOI
  34. Cornejo-Páramo, 2020, Viviparous reptile regarded to have temperature-dependent sex determination has old XY chromosomes, Genome Biol. Evol., 12, 924, 10.1093/gbe/evaa104 · DOI
  35. Wiggins, 2020, Gene dose indicates presence of sex chromosomes in collared lizards (Crotaphytus collaris), a species with temperature-influenced sex determination, Herpetologica, 76, 27, 10.1655/Herpetologica-D-19-00036 · DOI
  36. Mazzoleni, 2019, Turtles of the genera Geoemyda and Pangshura (Testudines: Geoemydidae) lack differentiated sex chromosomes: the end of a 40-year error cascade for Pangshura, PeerJ, 7, e6241, 10.7717/peerj.6241 · DOI
  37. Srikulnath, 2014, Identification of the linkage group of the Z sex chromosomes of the sand lizard (Lacerta agilis, Lacertidae) and elucidation of karyotype evolution in lacertid lizards, Chromosoma, 123, 563, 10.1007/s00412-014-0467-8 · DOI
  38. Lisachov, 2020, Chromosome painting does not support a sex chromosome turnover in Lacerta agilis Linnaeus, 1758, Cytogenet. Genome Res., 160, 134, 10.1159/000506321 · DOI
  39. Matsubara, 2006, Evidence for different origin of sex chromosomes in snakes, birds, and mammals and step-wise differentiation of snake sex chromosomes, Proc. Natl Acad. Sci. USA, 103, 18 190, 10.1073/pnas.0605274103 · DOI
  40. Vicoso, 2013, Comparative sex chromosome genomics in snakes: differentiation, evolutionary strata, and lack of global dosage compensation, PLoS Biol., 11, e1001643, 10.1371/journal.pbio.1001643 · DOI
  41. Gamble, 2017, The discovery of XY sex chromosomes in a boa and python, Curr. Biol., 27, 2148, 10.1016/j.cub.2017.06.010 · DOI
  42. Augstenová, 2018, ZW, XY, and yet ZW: sex chromosome evolution in snakes even more complicated, Evolution, 72, 1701, 10.1111/evo.13543 · DOI
  43. Pokorná, 2014, Sex chromosomes and karyotype of the (nearly) mythical creature, the Gila monster, Heloderma suspectum (Squamata: Helodermatidae), PLoS ONE, 9, e104716, 10.1371/journal.pone.0104716 · DOI
  44. Rovatsos, 2019, Shared ancient sex chromosomes in varanids, beaded lizards, and alligator lizards, Mol. Biol. Evol., 36, 1113, 10.1093/molbev/msz024 · DOI
  45. Nielsen, 2020, First report of sex chromosomes in night lizards (Scincoidea: Xantusiidae), J. Hered., 111, 307, 10.1093/jhered/esaa007 · DOI
  46. Pokorná, 2014, A ZZ/ZW sex chromosome system in the thick-tailed gecko (Underwoodisaurus milii; Squamata: Gekkota: Carphodactylidae), a member of the ancient gecko lineage, Cytogenet. Genome Res., 142, 190, 10.1159/000358847 · DOI
  47. Gamble, 2015, Restriction site-associated DNA sequencing (RAD-seq) reveals an extraordinary number of transitions among gecko sex-determining systems, Mol. Biol. Evol., 32, 1296, 10.1093/molbev/msv023 · DOI
  48. Keating, 2020, Conserved ZZ/ZW sex chromosomes in Caribbean croaking geckos (Aristelliger: Sphaerodactylidae), J. Evol. Biol., 33, 1316, 10.1111/jeb.13682 · DOI
  49. Pensabene, 2020, Independent evolution of sex chromosomes in eublepharid geckos, a lineage with environmental and genotypic sex determination, Life, 10, 342, 10.3390/life10120342 · DOI
  50. Rovatsos, 2014, Cretaceous park of sex determination: sex chromosomes are conserved across iguanas, Biol. Lett., 10, 20131093, 10.1098/rsbl.2013.1093 · DOI
  51. Altmanová, 2018, All iguana families with the exception of basilisks share sex chromosomes, Zoology, 126, 98, 10.1016/j.zool.2017.11.007 · DOI
  52. Rovatsos, 2015, Evolutionary stability of sex chromosomes in snakes, Proc. R. Soc. B, 282, 20151992, 10.1098/rspb.2015.1992 · DOI
  53. Rovatsos, 2017, Stable cretaceous sex chromosomes enable molecular sexing in softshell turtles (Testudines: Trionychidae), Sci. Rep., 7, 42150, 10.1038/srep42150 · DOI
  54. Rovatsos, 2021, Do male and female heterogamety really differ in expression regulation? Lack of global dosage balance in pygopodid geckos, Phil. Trans. R. Soc. B, 376, 20200102, 10.1098/rstb.2020.0102 · DOI
  55. Augstenová, Are geckos special in sex determination? Independently evolved differentiated ZZ/ZW sex chromosomes in carphodactylid geckos, Genome Biol. Evol.
  56. Ezaz, 2009, Molecular marker suggests rapid changes of sex-determining mechanisms in Australian dragon lizards, Chromosome Res., 17, 91, 10.1007/s10577-008-9019-5 · DOI
  57. Bókony, 2019, Sex ratios and bimaturism differ between temperature-dependent and genetic sex-determination systems in reptiles, BMC Evol. Biol., 19, 57, 10.1186/s12862-019-1386-3 · DOI
  58. Pokorná, 2009, Phylogeny of sex-determining mechanisms in squamate reptiles: are sex chromosomes an evolutionary trap?, Zool. J. Linn. Soc., 156, 168, 10.1111/j.1096-3642.2008.00481.x · DOI
  59. Bista, 2020, Turtle insights into the evolution of the reptilian karyotype and the genomic architecture of sex determination, Genes, 11, 416, 10.3390/genes11040416 · DOI
  60. González, 2019, The sex-determination pattern in crocodilians: a systematic review of three decades of research, J. Anim. Ecol., 88, 1417, 10.1111/1365-2656.13037 · DOI
  61. Grützner, 2004, In the platypus a meiotic chain of ten sex chromosomes shares genes with the bird Z and mammal X chromosomes, Nature, 432, 913, 10.1038/nature03021 · DOI
  62. Rens, 2007, The multiple sex chromosomes of platypus and echidna are not completely identical and several share homology with the avian Z, Genome Biol., 8, R243, 10.1186/gb-2007-8-11-r243 · DOI · Paper page
  63. Kawai, 2009, The ZW sex chromosomes of Gekko hokouensis (Gekkonidae, Squamata) represent highly conserved homology with those of avian species, Chromosoma, 118, 43, 10.1007/s00412-008-0176-2 · DOI
  64. Zechner, 2011, Sex chromosomes in vertebrates: XX/XY against ZZ/ZW, Sex Dev., 5, 266, 10.1159/000331233 · DOI
  65. Pokorná, 2016, What was the ancestral sex-determining mechanism in amniote vertebrates?, Biol. Rev., 91, 1, 10.1111/brv.12156 · DOI
  66. Singchat, 2018, Chromosome map of the Siamese cobra: did partial synteny of sex chromosomes in the amniote represent ‘a hypothetical ancestral super-sex chromosome’ or random distribution?, BMC Genomics, 19, 939, 10.1186/s12864-018-5293-6 · DOI
  67. Singchat, 2020, Snake W sex chromosome: the shadow of ancestral amniote super-sex chromosome, Cells, 9, E2386, 10.3390/cells9112386 · DOI
  68. Laopichienpong, 2020, Genome-wide SNP analysis of Siamese cobra (Naja kaouthia) reveals the molecular basis of transitions between Z and W sex chromosomes and supports the presence of an ancestral super-sex chromosome in amniotes, Genomics, 13, 624
  69. Smith, 2007, Bird and mammal sex-chromosome orthologs map to the same autosomal region in a salamander (Ambystoma), Genetics, 177, 607, 10.1534/genetics.107.072033 · DOI
  70. Voss, 2011, Origin of amphibian and avian chromosomes by fission, fusion, and retention of ancestral chromosomes, Genome Res., 21, 1306, 10.1101/gr.116491.110 · DOI
  71. Suryamohan, 2020, The Indian cobra reference genome and transcriptome enables comprehensive identification of venom toxins, Nat. Genet., 52, 106, 10.1038/s41588-019-0559-8 · DOI
  72. Bellott, 2010, Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition, Nature, 466, 612, 10.1038/nature09172 · DOI
  73. Ellegren, 2011, Emergence of male-biased genes on the chicken Z-chromosome: sex-chromosome contrasts between male and female heterogametic systems, Genome Res., 21, 2082, 10.1101/gr.119065.110 · DOI
  74. Altmanová, 2016, Minute Y chromosomes and karyotype evolution in Madagascan iguanas (Squamata: Iguania: Opluridae), Biol. J. Linn. Soc., 118, 618, 10.1111/bij.12751 · DOI
  75. Pokorná, 2016, First description of the karyotype and sex chromosomes in the Komodo dragon (Varanus komodoensis), Cytogenet. Genome Res., 148, 284, 10.1159/000447340 · DOI
  76. Suwala, 2020, Evolutionary variability of W-linked repetitive content in lacertid lizards, Genes, 11, 531, 10.3390/genes11050531 · DOI
  77. Pokorná, 2011, Microsatellite distribution on sex chromosomes at different stages of heteromorphism and heterochromatinization in two lizard species (Squamata: Eublepharidae: Coleonyx elegans and Lacertidae: Eremias velox), BMC Genet., 12, 90, 10.1186/1471-2156-12-90 · DOI
  78. Rovatsos, 2015, Interstitial telomeric motifs in squamate reptiles: when the exceptions outnumber the rule, PLoS ONE, 10, e0134985, 10.1371/journal.pone.0134985 · DOI
  79. Matsubara, 2016, Amplification of microsatellite repeat motifs is associated with the evolutionary differentiation and heterochromatinization of sex chromosomes in Sauropsida, Chromosoma, 125, 111, 10.1007/s00412-015-0531-z · DOI
  80. Augstenová, 2019, Cytogenetic analysis did not reveal differentiated sex chromosomes in ten species of boas and pythons (Reptilia: Serpentes), Genes, 10, 934, 10.3390/genes10110934 · DOI
  81. Pan, 2021, Evolution of master sex determiners: TGF-β signalling pathways at regulatory crossroads, Phil. Trans. R. Soc. B, 376, 20200091, 10.1098/rstb.2020.0091 · DOI
  82. Beukeboom, 2014, The evolution of sex determination, 10.1093/acprof:oso/9780199657148.001.0001 · DOI
  83. Ge, 2018, The histone demethylase KDM6B regulates temperature-dependent sex determination in a turtle species, Science, 360, 645, 10.1126/science.aap8328 · DOI · Paper page
  84. Weber, 2021, Sex determination without sex chromosomes, Phil. Trans. R. Soc. B, 376, 20200109, 10.1098/rstb.2020.0109 · DOI
  85. Holleley, 2015, Sex reversal triggers the rapid transition from genetic to temperature-dependent sex, Nature, 523, 79, 10.1038/nature14574 · DOI
  86. Quinn, 2010, Extension, single-locus conversion and physical mapping of sex chromosome sequences identify the Z microchromosome and pseudo-autosomal region in a dragon lizard, Pogona vitticeps, Heredity, 104, 410, 10.1038/hdy.2009.133 · DOI
  87. Ehl, With or without W? Molecular and cytogenetic markers are not sufficient for identification of environmentally-induced sex reversals in the bearded dragon, Sex Dev.
  88. Tonini, 2016, Fully-sampled phylogenies of squamates reveal evolutionary patterns in threat status, Biol. Conserv., 204, 23, 10.1016/j.biocon.2016.03.039 · DOI
  89. Catchen, 2009, Automated identification of conserved synteny after whole-genome duplication, Genome Res., 19, 1497, 10.1101/gr.090480.108 · DOI
  90. Ruiz-Herrera, 2012, Molecular cytogenetic and genomic insights into chromosomal evolution, Heredity, 108, 28, 10.1038/hdy.2011.102 · DOI
  91. Zimmermann, 2019, Ancient animal genome architecture reflects cell type identities, Nat. Evol. Evol., 3, 1289, 10.1038/s41559-019-0946-7 · DOI
  92. Pokorná, 2012, Conservation of chromosomes syntenic with avian autosomes in squamate reptiles revealed by comparative chromosome painting, Chromosoma, 121, 409, 10.1007/s00412-012-0371-z · DOI
  93. Lind, 2019, Genome of the Komodo dragon reveals adaptations in the cardiovascular and chemosensory systems of monitor lizards, Nat. Ecol. Evol., 3, 1241, 10.1038/s41559-019-0945-8 · DOI
  94. Schield, 2019, The origins and evolution of chromosomes, dosage compensation, and mechanisms underlying venom regulation in snakes, Genome Res., 29, 590, 10.1101/gr.240952.118 · DOI
  95. Simison, 2020, An annotated chromosome-level reference genome of the red-eared slider turtle (Trachemys scripta elegans), Genome Biol. Evol., 12, 456, 10.1093/gbe/evaa063 · DOI
  96. Yurchenko, 2020, Chromosome-level assembly of the common lizard (Zootoca vivipara) genome, Genome Biol. Evol., 12, 1953, 10.1093/gbe/evaa161 · DOI
  97. Wilcox, 1996, Comparative mapping identifies the fusion point of an ancient mammalian X-autosomal rearrangement, Genomics, 35, 66, 10.1006/geno.1996.0323 · DOI
  98. Nanda, 1999, 300 million years of conserved synteny between chicken Z and human chromosome 9, Nat. Genet., 21, 258, 10.1038/6769 · DOI
  99. Farré, 2019, Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks, Genome Res., 29, 576, 10.1101/gr.239863.118 · DOI
  100. Sigeman, 2019, Repeated sex chromosome evolution in vertebrates supported by expanded avian sex chromosomes, Proc. R. Soc. B, 286, 20192051, 10.1098/rspb.2019.2051 · DOI
  101. O'Connor, 2018, Reconstruction of the diapsid ancestral genome permits chromosome evolution tracing in avian and non-avian dinosaurs, Nat. Commun.., 9, 1883, 10.1038/s41467-018-04267-9 · DOI
  102. Damas, 2018, Reconstruction of avian ancestral karyotypes reveals differences in the evolutionary history of macro- and microchromosomes, Genome Biol., 19, 155, 10.1186/s13059-018-1544-8 · DOI
  103. Griffin, 2007, The evolution of the avian genome as revealed by comparative molecular cytogenetics, Cytogenet. Genome Res., 117, 64, 10.1159/000103166 · DOI
  104. Warren, 2017, A new chicken genome assembly provides insight into avian genome structure, G3: Genes Genom. Genet., 7, 109, 10.1534/g3.116.035923 · DOI
  105. R Core Team, 2020, R: a language and environment for statistical computing
  106. Sutton, 2011, Identification of SOX3 as an XX male sex reversal gene in mice and humans, J. Clin. Invest., 121, 328, 10.1172/JCI42580 · DOI
  107. Masuyama, 2012, Dmrt1 mutation causes a male-to-female sex reversal after the sex determination by Dmy in the medaka, Chromosome Res., 20, 163, 10.1007/s10577-011-9264-x · DOI
  108. Oike, 2017, Participation of androgen and its receptor in sex determination of an amphibian species, PLoS ONE, 12, e0178067, 10.1371/journal.pone.0178067 · DOI
  109. Werner, 2017, New NR5A1 mutations and phenotypic variations of gonadal dysgenesis, PLoS ONE, 12, e0176720, 10.1371/journal.pone.0176720 · DOI
  110. Lin, 2017, Distinct and cooperative roles of amh and dmrt1 in self-renewal and differentiation of male germ cells in zebrafish, Genetics, 207, 1007, 10.1534/genetics.117.300274 · DOI
  111. Kumar, 2014, ‘Been hit twice’: a novel bi-allelic heterozygous mutation in LHCGR, J. Assist. Reprod. Genet., 31, 783, 10.1007/s10815-014-0284-2 · DOI
  112. Zhang, 2015, Disruption of zebrafish follicle-stimulating hormone receptor (fshr) but not luteinizing hormone receptor (lhcgr) gene by TALEN leads to failed follicle activation in females followed by sexual reversal to males, Endocrinology, 156, 3747, 10.1210/en.2015-1039 · DOI
  113. Pan, 2019, Identification of the master sex determining gene in northern pike (Esox lucius) reveals restricted sex chromosome differentiation, PLoS Genet., 15, e1008013, 10.1371/journal.pgen.1008013 · DOI
  114. Sinclair, 1990, A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif, Nature, 346, 240, 10.1038/346240a0 · DOI
  115. Smith, 2009, The avian Z-linked gene DMRT1 is required for male sex determination in the chicken, Nature, 461, 267, 10.1038/nature08298 · DOI
  116. Ioannidis, 2020, Primary sex determination in birds depends on DMRT1 dosage, but gonadal sex does not determine secondary sexual characteristics, Proc. Natl Acad. Sci. USA, 118, e2020909118, 10.1073/pnas.2020909118 · DOI
  117. van Doorn, 2007, Turnover of sex chromosomes induced by sexual conflict, Nature, 449, 909, 10.1038/nature06178 · DOI
  118. Lisachov, 2019, Genetic content of the neo-sex chromosomes in Ctenonotus and Norops (Squamata, Dactyloidae) and degeneration of the Y chromosome as revealed by high-throughput sequencing of individual chromosomes, Cytogenet. Genome Res., 157, 115, 10.1159/000497091 · DOI
  119. Lisachov, 2021, Whole-chromosome fusions in the karyotype evolution of Sceloporus (Iguania, Reptilia) are more frequent in sex chromosomes than autosomes, Phil. Trans. R. Soc. B, 376, 20200099, 10.1098/rstb.2020.0099 · DOI
  120. O'Brien, 2020, Atlas of mammalian chromosomes
  121. Pokorná, 2014, Multiple sex chromosomes in the light of female meiotic drive in amniote vertebrates, Chromosome Res., 22, 35, 10.1007/s10577-014-9403-2 · DOI
  122. Gunski, 2017, Multiple sex chromosome system in penguins (Pygoscelis, Spheniscidae), Comp. Cytogenet., 11, 541, 10.3897/CompCytogen.v11i3.13795 · DOI
  123. Gan, 2019, Genomic evidence of neo-sex chromosomes in the eastern yellow robin, GigaScience, 8, giz111, 10.1093/gigascience/giz111 · DOI
  124. Rovatsos, 2021, Evolution of dosage compensation does not depend on genomic background, Mol. Ecol., 30, 1836, 10.1111/mec.15853 · DOI
  125. Rovatsos, 2016, Mammalian X homolog acts as sex chromosome in lacertid lizards, Heredity, 117, 8, 10.1038/hdy.2016.18 · DOI

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Metadata

Authors
Kratochvíl, L., Gamble, T., & Rovatsos, M.
Affiliations
  • Department of Ecology, Faculty of Science 1 , ,
  • Department of Biological Sciences 2 , ,
ORCID
Venue
Philosophical Transactions of the Royal Society B
Publisher
The Royal Society
Published
2021-07-26
Volume
376
Issue
1833
ISSN
  • 0962-8436
  • 1471-2970
DOI
10.1098/rstb.2020.0108
Cited by
48
References
1
Language
en
Licence
Funders
  • Univerzita Karlova v Praze (PRIMUS/SCI/46)
  • Grantová Agentura České Republiky (17-22604S)

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