The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Sex chromosome evolution among amniotes: is the origin of sex chromosomes non-random?
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)’.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“While the same or similar genomic regions often recurrently evolve into sex chromosomes, perhaps due to ancestral gene functions involved in gonadogenesis, evidence about the nonrandomness of sex chromosome evolution is still contentious (Kratochvíl et al., 2021).”
From GENESPACE tracks regions of interest and gene copy number variation across multiple genomes (2022) · cites this paper as Kratochvíl et al., 2021
Citations
Cites
Deveson, I. W., Holleley, C. E., Blackburn, J., Marshall Graves, J. A., Mattick, J. S., Waters, P. D., & Georges, A. (2017) · Science Advances · doi:10.1126/sciadv.1700731 · Cited by 132
Research works printed but not linked: 125
- Bull, 1983, Evolution of sex determining mechanisms
- Capel, 2019, Sex determination in vertebrates
- Straková, 2020, Evolution of sex determination in amniotes: did stress and sequential hermaphroditism produce environmental determination?, BioEssays, 42, e2000050, 10.1002/bies.202000050 · DOI
- Ohno, 1967, Sex chromosomes and sex-linked Genes, 10.1007/978-3-642-88178-7 · DOI
- Charlesworth, 2005, Steps in the evolution of heteromorphic sex chromosomes, Heredity, 95, 118, 10.1038/sj.hdy.6800697 · DOI
- Fisher, 1931, The evolution of dominance, Biol. Rev., 6, 345, 10.1111/j.1469-185X.1931.tb01030.x · DOI
- Rice, 1984, Sex chromosomes and the evolution of sexual dimorphism, Evolution, 38, 735, 10.1111/j.1558-5646.1984.tb00346.x · DOI
- Furman, 2020, Sex chromosome evolution: so many exceptions to the rules, Genome Biol. Evol., 12, 750, 10.1093/gbe/evaa081 · DOI
- Myosho, 2015, Turnover of sex chromosomes in celebensis group Medaka fishes, G3: Genes Genom. Genet., 5, 2685, 10.1534/g3.115.021543 · DOI
- 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
- Lichilín, 2021, Sex-biased gene expression and recent sex chromosome turnover, Phil. Trans. R. Soc. B, 376, 20200107, 10.1098/rstb.2020.0107 · DOI
- 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
- 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
- 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
- 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
- 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
- O'Meally, 2012, Are some chromosomes particularly good at sex? Insights from amniotes, Chromosome Res., 20, 7, 10.1007/s10577-011-9266-8 · DOI
- Livernois, 2012, The origin and evolution of vertebrate sex chromosomes and dosage compensation, Heredity, 108, 50, 10.1038/hdy.2011.106 · DOI
- Ezaz, 2017, Origin of amniote sex chromosomes: an ancestral super-sex chromosome, or common requirements?, J. Heredity, 108, 94, 10.1093/jhered/esw053 · DOI
- Rovatsos, 2019, The rise and fall of differentiated sex chromosomes in geckos, Mol. Ecol., 28, 3042, 10.1111/mec.15126 · DOI
- Cortez, 2014, Origins and functional evolution of Y chromosomes across mammals, Nature, 508, 488, 10.1038/nature13151 · DOI
- Zhou, 2014, Complex evolutionary trajectories of sex chromosomes across bird taxa, Science, 346, 1246338, 10.1126/science.1246338 · DOI · Paper page
- Sarre, 2004, The ends of a continuum: genetic and temperature-dependent sex determination in reptiles, BioEssays, 26, 639, 10.1002/bies.20050 · DOI
- Grossen, 2011, Temperature-dependent turnovers in sex-determination mechanisms: a quantitative model, Evolution, 65, 64, 10.1111/j.1558-5646.2010.01098.x · DOI
- Kumar, 2017, TimeTree: a resource for timelines, timetrees, and divergence times, Mol. Biol. Evol., 34, 1812, 10.1093/molbev/msx116 · DOI
- 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
- 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
- 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
- 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
- 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
- Telemeco, 2015, Sex determination in southern alligator lizards (Elgaria multicarinata; Anguidae), Herpetologica, 71, 8, 10.1655/Herpetologica-D-14-00033 · DOI
- Nielsen, 2018, Dynamic sex chromosomes in Old World chameleons (Squamata: Chamaeleonidae), J. Evol. Biol., 31, 484, 10.1111/jeb.13242 · DOI
- Iannucci, 2019, Conserved sex chromosomes and karyotype evolution in monitor lizards (Varanidae), Heredity, 123, 215, 10.1038/s41437-018-0179-6 · DOI
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Augstenová, 2018, ZW, XY, and yet ZW: sex chromosome evolution in snakes even more complicated, Evolution, 72, 1701, 10.1111/evo.13543 · DOI
- 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
- Rovatsos, 2019, Shared ancient sex chromosomes in varanids, beaded lizards, and alligator lizards, Mol. Biol. Evol., 36, 1113, 10.1093/molbev/msz024 · DOI
- Nielsen, 2020, First report of sex chromosomes in night lizards (Scincoidea: Xantusiidae), J. Hered., 111, 307, 10.1093/jhered/esaa007 · DOI
- 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
- 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
- Keating, 2020, Conserved ZZ/ZW sex chromosomes in Caribbean croaking geckos (Aristelliger: Sphaerodactylidae), J. Evol. Biol., 33, 1316, 10.1111/jeb.13682 · DOI
- 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
- Rovatsos, 2014, Cretaceous park of sex determination: sex chromosomes are conserved across iguanas, Biol. Lett., 10, 20131093, 10.1098/rsbl.2013.1093 · DOI
- Altmanová, 2018, All iguana families with the exception of basilisks share sex chromosomes, Zoology, 126, 98, 10.1016/j.zool.2017.11.007 · DOI
- Rovatsos, 2015, Evolutionary stability of sex chromosomes in snakes, Proc. R. Soc. B, 282, 20151992, 10.1098/rspb.2015.1992 · DOI
- Rovatsos, 2017, Stable cretaceous sex chromosomes enable molecular sexing in softshell turtles (Testudines: Trionychidae), Sci. Rep., 7, 42150, 10.1038/srep42150 · DOI
- 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
- Augstenová, Are geckos special in sex determination? Independently evolved differentiated ZZ/ZW sex chromosomes in carphodactylid geckos, Genome Biol. Evol.
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- Zechner, 2011, Sex chromosomes in vertebrates: XX/XY against ZZ/ZW, Sex Dev., 5, 266, 10.1159/000331233 · DOI
- Pokorná, 2016, What was the ancestral sex-determining mechanism in amniote vertebrates?, Biol. Rev., 91, 1, 10.1111/brv.12156 · DOI
- 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
- Singchat, 2020, Snake W sex chromosome: the shadow of ancestral amniote super-sex chromosome, Cells, 9, E2386, 10.3390/cells9112386 · DOI
- 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
- 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
- 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
- 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
- Bellott, 2010, Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition, Nature, 466, 612, 10.1038/nature09172 · DOI
- 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
- 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
- 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
- Suwala, 2020, Evolutionary variability of W-linked repetitive content in lacertid lizards, Genes, 11, 531, 10.3390/genes11050531 · DOI
- 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
- Rovatsos, 2015, Interstitial telomeric motifs in squamate reptiles: when the exceptions outnumber the rule, PLoS ONE, 10, e0134985, 10.1371/journal.pone.0134985 · DOI
- 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
- 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
- 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
- Beukeboom, 2014, The evolution of sex determination, 10.1093/acprof:oso/9780199657148.001.0001 · DOI
- 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
- Weber, 2021, Sex determination without sex chromosomes, Phil. Trans. R. Soc. B, 376, 20200109, 10.1098/rstb.2020.0109 · DOI
- Holleley, 2015, Sex reversal triggers the rapid transition from genetic to temperature-dependent sex, Nature, 523, 79, 10.1038/nature14574 · DOI
- 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
- 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.
- 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
- Catchen, 2009, Automated identification of conserved synteny after whole-genome duplication, Genome Res., 19, 1497, 10.1101/gr.090480.108 · DOI
- Ruiz-Herrera, 2012, Molecular cytogenetic and genomic insights into chromosomal evolution, Heredity, 108, 28, 10.1038/hdy.2011.102 · DOI
- Zimmermann, 2019, Ancient animal genome architecture reflects cell type identities, Nat. Evol. Evol., 3, 1289, 10.1038/s41559-019-0946-7 · DOI
- 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
- 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
- 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
- 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
- Yurchenko, 2020, Chromosome-level assembly of the common lizard (Zootoca vivipara) genome, Genome Biol. Evol., 12, 1953, 10.1093/gbe/evaa161 · DOI
- Wilcox, 1996, Comparative mapping identifies the fusion point of an ancient mammalian X-autosomal rearrangement, Genomics, 35, 66, 10.1006/geno.1996.0323 · DOI
- Nanda, 1999, 300 million years of conserved synteny between chicken Z and human chromosome 9, Nat. Genet., 21, 258, 10.1038/6769 · DOI
- 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
- 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
- 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
- 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
- Griffin, 2007, The evolution of the avian genome as revealed by comparative molecular cytogenetics, Cytogenet. Genome Res., 117, 64, 10.1159/000103166 · DOI
- 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
- R Core Team, 2020, R: a language and environment for statistical computing
- 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
- 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
- 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
- Werner, 2017, New NR5A1 mutations and phenotypic variations of gonadal dysgenesis, PLoS ONE, 12, e0176720, 10.1371/journal.pone.0176720 · DOI
- 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
- 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
- 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
- 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
- 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
- Smith, 2009, The avian Z-linked gene DMRT1 is required for male sex determination in the chicken, Nature, 461, 267, 10.1038/nature08298 · DOI
- 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
- van Doorn, 2007, Turnover of sex chromosomes induced by sexual conflict, Nature, 449, 909, 10.1038/nature06178 · DOI
- 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
- 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
- O'Brien, 2020, Atlas of mammalian chromosomes
- 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
- Gunski, 2017, Multiple sex chromosome system in penguins (Pygoscelis, Spheniscidae), Comp. Cytogenet., 11, 541, 10.3897/CompCytogen.v11i3.13795 · DOI
- Gan, 2019, Genomic evidence of neo-sex chromosomes in the eastern yellow robin, GigaScience, 8, giz111, 10.1093/gigascience/giz111 · DOI
- Rovatsos, 2021, Evolution of dosage compensation does not depend on genomic background, Mol. Ecol., 30, 1836, 10.1111/mec.15853 · DOI
- Rovatsos, 2016, Mammalian X homolog acts as sex chromosome in lacertid lizards, Heredity, 117, 8, 10.1038/hdy.2016.18 · DOI
Cited by
Sorted by citations
GENESPACE tracks regions of interest and gene copy number variation across multiple genomes
Lovell, J. T., Sreedasyam, A., Schranz, M. E., Wilson, M., Carlson, J. W., Harkess, A., Emms, D., Goodstein, D. M., & Schmutz, J. (2022) · eLife · doi:10.7554/elife.78526 · Cited by 391
Metadata
- Authors
- Kratochvíl, L., Gamble, T., & Rovatsos, M.
- Affiliations
- Department of Ecology, Faculty of Science 1 , ,
- Department of Biological Sciences 2 , ,
- 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
- Cited by
- 48
- References
- 1
- Language
- en
- Licence
- Funders
- Univerzita Karlova v Praze (PRIMUS/SCI/46)
- Grantová Agentura České Republiky (17-22604S)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review