Abstract

Sex chromosomes are unique genomic regions with sex-specific or sex-biased inherent patterns and are expected to be more frequently subject to sex-specific selection. Substantial knowledge on the evolutionary patterns of sex-linked genes have been gained from the studies on the male heterogametic systems (XY male, XX female), but the understanding of the role of sex-specific selection in the evolution of female-heterogametic sex chromosomes (ZW female, ZZ male) is limited. Here we collect the W-linked genes of 27 birds, covering the three major avian clades: Neoaves (songbirds), Galloanserae (chicken), and Palaeognathae (ratites and tinamous). We find that the avian W chromosomes exhibit very conserved gene content despite their independent evolution of recombination suppression. The retained W-linked genes have higher dosage-sensitive and higher expression level than the lost genes, suggesting the role of purifying selection in their retention. Moreover, they are not enriched in ancestrally female-biased genes, and have not acquired new ovary-biased expression patterns after becoming W-linked. They are broadly expressed across female tissues, and the expression profile of the W-linked genes in females is not deviated from that of the homologous Z-linked genes. Together, our new analyses suggest that female-specific positive selection on the avian W chromosomes is limited, and the gene content of the W chromosomes is mainly shaped by purifying selection.

Highlights

  • Sex chromosomes evolve in a distinctive manner from the rest of the genome, of which one (Y or W) chromosome is sex-limited except for the pseudoautosomal regions (PAR), while the other homologous (X or Z) chromosome is biasedly inherited in one of the sexes

  • We focused on the genes that are homologous to the bird sex-linked genes, and because they are autosomal in green anole, their expression represents the ancestral expression in the bird proto-sex chromosomes

  • To investigate the extent of the W chromosome decay, first we demarcated the boundary of the pseudoautosomal regions (PARs) and the differentiation regions (DRs) according to the female coverage along the Z

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Summary

Introduction

Sex chromosomes evolve in a distinctive manner from the rest of the genome, of which one (Y or W) chromosome is sex-limited except for the pseudoautosomal regions (PAR), while the other homologous (X or Z) chromosome is biasedly inherited in one of the sexes. Once the sex-linked regions cease homologous recombination on the Y or W chromosome in the heterogametic sex, they are usually subject to functional degeneration [1]. The degeneration process can be caused by various evolutionary mechanisms including genetic hitchhiking [2], Muller’s ratchet [3], and background selection [4]. Due to the sex-limited or biased inheritance, sex chromosomes are hypothesized to be a preferred genomic location for the sexual antagonistic (SA) alleles to accumulate [9,10].

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