MOE Laboratory of Biosystems Homeostasis and Protection and Zhejiang Provincial Key Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, Zhejiang 310058, China; Department of Neuroscience and Developmental Biology, University of Vienna, Vienna 1090, Austria; Institute of Animal Sex and Development, Zhejiang Wanli University, Ningbo, Zhejiang 315100, China; BGI-Shenzhen, Beishan Industrial Zone, Shenzhen 518083, China.
Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77 Stockholm, Sweden.
J Genet Genomics. 2022 Feb;49(2):109-119. doi: 10.1016/j.jgg.2021.06.013. Epub 2021 Jul 13.
Many paleognaths (ratites and tinamous) have a pair of homomorphic ZW sex chromosomes in contrast to the highly differentiated sex chromosomes of most other birds. To understand the evolutionary causes for the different tempos of sex chromosome evolution, we produced female genomes of 12 paleognathous species and reconstructed the phylogeny and the evolutionary history of paleognathous sex chromosomes. We uncovered that Palaeognathae sex chromosomes had undergone stepwise recombination suppression and formed a pattern of "evolutionary strata". Nine of the 15 studied species' sex chromosomes have maintained homologous recombination in their long pseudoautosomal regions extending more than half of the entire chromosome length. We found that in the older strata, the W chromosome suffered more serious functional gene loss. Their homologous Z-linked regions, compared with other genomic regions, have produced an excess of species-specific autosomal duplicated genes that evolved female-specific expression, in contrast to their broadly expressed progenitors. We speculate such "defeminization" of Z chromosome with underrepresentation of female-biased genes and slow divergence of sex chromosomes of paleognaths might be related to their distinctive mode of sexual selection targeting females rather than males, which evolved in their common ancestors.
许多古颚总目鸟类(平胸鸟类和鸵鸟目)具有一对形态相同的 ZW 性染色体,而大多数其他鸟类的性染色体则高度分化。为了了解导致性染色体进化速度不同的进化原因,我们生成了 12 种古颚总目鸟类的雌性基因组,并重建了古颚总目鸟类性染色体的系统发育和进化历史。我们发现,古颚总目鸟类的性染色体经历了逐步的重组抑制,并形成了“进化层”的模式。在研究的 15 个物种中,有 9 个物种的性染色体在其长的假常染色体区域中保持着同源重组,这些区域延伸超过整个染色体长度的一半。我们发现,在较老的层中,W 染色体遭受了更严重的功能基因丢失。与其他基因组区域相比,它们的同源 Z 连锁区域产生了过多的物种特异性常染色体重复基因,这些基因表现出雌性特异性表达,而不是它们的广泛表达祖先。我们推测,古颚总目鸟类的性染色体的“去雌性化”,即雌性偏性基因的代表性不足,以及性染色体的缓慢分化,可能与它们独特的雌性选择模式有关,这种模式是在它们的共同祖先中进化而来的,而不是针对雄性。