Abstract:Work on the evolution of sex chromosomes and sex determination in the Meisel lab is supported by the National Science Foundation under Grant No. DEB-1845686.
“…In terms of chromosome evolution, this is reflected in the suppressed recombination between sex chromosomes 1 . The non-recombing regions of the W chromosome are severely degenerated due to increased sexual antagonism and the low efficiency of natural selection, resulting from Muller's ratchet and the Hill-Robertson effect 5,15,78 . In bird species with female heterogamety (ZW system), sexual dimorphism and maletargeted sexual selection 79,80 led to the excess accumulation of male fitness mutations on the Z chromosome, promoting a faster evolutionary rate for the Z chromosome, which is known as the 'fast-Z' effect 81,82 .…”
Section: Discussionmentioning
confidence: 99%
“…In most birds and mammals, sex is determined by a pair of heteromorphic sex chromosomes (Z-W in birds and X-Y in mammals) that differ in morphology, size, and gene content 3,4 . In most birds and mammals, the Z and X chromosomes, respectively, are evolutionarily conserved, with relatively stable structures and gene contents 5,6 , while the sexlimited W and Y chromosomes exhibit a high degree of heterochromatinization and typically contain only a few genes due to the lack of recombination 2,[7][8][9] .…”
Bird sex chromosomes play a unique role in sex-determination, and affect the sexual morphology and behavior of bird species. Core waterbirds, a major clade of birds, share the common characteristics of being sexually monomorphic and having lower levels of inter-sexual conflict, yet their sex chromosome evolution remains poorly understood. Here, by we analyse of a chromosome-level assembly of a female crested ibis (Nipponia nippon), a typical core waterbird. We identify neo-sex chromosomes resulting from fusion of microchromosomes with ancient sex chromosomes. These fusion events likely occurred following the divergence of Threskiornithidae and Ardeidae. The neo-W chromosome of the crested ibis exhibits the characteristics of slow degradation, which is reflected in its retention of abundant gametologous genes. Neo-W chromosome genes display an apparent ovary-biased gene expression, which is largely driven by genes that are retained on the crested ibis W chromosome but lost in other bird species. These results provide new insights into the evolutionary history and expression patterns for the sex chromosomes of bird species.
“…In terms of chromosome evolution, this is reflected in the suppressed recombination between sex chromosomes 1 . The non-recombing regions of the W chromosome are severely degenerated due to increased sexual antagonism and the low efficiency of natural selection, resulting from Muller's ratchet and the Hill-Robertson effect 5,15,78 . In bird species with female heterogamety (ZW system), sexual dimorphism and maletargeted sexual selection 79,80 led to the excess accumulation of male fitness mutations on the Z chromosome, promoting a faster evolutionary rate for the Z chromosome, which is known as the 'fast-Z' effect 81,82 .…”
Section: Discussionmentioning
confidence: 99%
“…In most birds and mammals, sex is determined by a pair of heteromorphic sex chromosomes (Z-W in birds and X-Y in mammals) that differ in morphology, size, and gene content 3,4 . In most birds and mammals, the Z and X chromosomes, respectively, are evolutionarily conserved, with relatively stable structures and gene contents 5,6 , while the sexlimited W and Y chromosomes exhibit a high degree of heterochromatinization and typically contain only a few genes due to the lack of recombination 2,[7][8][9] .…”
Bird sex chromosomes play a unique role in sex-determination, and affect the sexual morphology and behavior of bird species. Core waterbirds, a major clade of birds, share the common characteristics of being sexually monomorphic and having lower levels of inter-sexual conflict, yet their sex chromosome evolution remains poorly understood. Here, by we analyse of a chromosome-level assembly of a female crested ibis (Nipponia nippon), a typical core waterbird. We identify neo-sex chromosomes resulting from fusion of microchromosomes with ancient sex chromosomes. These fusion events likely occurred following the divergence of Threskiornithidae and Ardeidae. The neo-W chromosome of the crested ibis exhibits the characteristics of slow degradation, which is reflected in its retention of abundant gametologous genes. Neo-W chromosome genes display an apparent ovary-biased gene expression, which is largely driven by genes that are retained on the crested ibis W chromosome but lost in other bird species. These results provide new insights into the evolutionary history and expression patterns for the sex chromosomes of bird species.
“…Structuring into small, geographically isolated populations may also facilitate sex chromosome differentiation and transition between sex chromosome systems (e.g., Primo et al, 2017;Cioffi et al, 2018;Krysanov & Demidova, 2018;Glugoski et al, 2020;Štundlová et al, 2022;Marajó et al, 2023) To answer the question whether indeed genetic drift is a major force in sex chromosomes fixation in Harttia and other fish lineages with similar eco-geographical and demographic features and whether certain selective forces and ecological factors (cf. Pennell et al, 2015;Veller et al, 2017;Saunders et al, 2018;Meisel, 2022) might have played a role in this process, we have to acquire much deeper knowledge especially concerning genetic content and degree of sex chromosome differentiation, presence/absence of sex chromosomes in wide range of conspecific populations, and their phylogenetic distribution based on well-resolved phylogeny (cf. Sember et al, 2021).…”
The remarkable fish biodiversity encompasses also great sex chromosome variability. Harttia catfish belong to Neotropical models for karyotype and sex chromosome research. Some species possess one of the three male-heterogametic sex chromosome systems, XY, X1X2Y or XY1Y2, while other members of the genus have yet uncharacterized modes of sex determination. Particularly the XY1Y2 multiple sex chromosome system shows a relatively low incidence among vertebrates, and it has not been yet thoroughly investigated. Previous research suggested two independent X-autosome fusions in Harttia which led to the emergence of XY1Y2 sex chromosome system in three of its species. In this study, we investigated evolutionary trajectories of synteny blocks involved in this XY1Y2 system by probing six Harttia species with whole chromosome painting (WCP) probes derived from the X (HCA-X) and the chromosome 9 (HCA-9) of H. carvalhoi. We found that both painting probes hybridize to two distinct chromosome pairs in Amazonian species, whereas the HCA-9 probe paints three chromosome pairs in H. guianensis, endemic to Guyanese drainages. These findings demonstrate distinct evolutionary fates of mapped synteny blocks and thereby elevated karyotype dynamics in Harttia among the three evolutionary clades.
“…Are there more factors contributing to the process of sex chromosome differentiation? Meisel (2022) argues that sex-specific selection in different habitats caused by sex-specific vulnerability to different environmental factors or pathogens, could lead to niche partitioning or different dietary strategies between sexes, which might affect the dynamics of sex chromosome evolution. The author goes on to suggest that the evolution of sex determination can be affected by ecological factors, especially in species where the sex determination pathway is sensitive to temperature, such as in some reptiles, teleost fishes and other vertebrates.…”
Section: Theme 5: Ecology and E Voluti On Of S E X Chromosome Smentioning
confidence: 99%
“…Future work should focus on identifying the underlying forces and genetic mechanisms driving sex chromosome turnovers. In addition, it should also focus on the importance of ecologically relevant selection pressure in sex chromosome turnovers (Meisel, 2022). Identifying how and what makes the sex-determining mechanisms so labile in certain lineages, but very stable in others, is still a challenge.…”
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