Evolutionary divergence between homologous X-Y chromosome genes shapes sex-biased biology

被引:3
作者
Decasien, Alex R. [1 ,2 ]
Tsai, Kathryn [1 ]
Liu, Siyuan [1 ]
Thomas, Adam [3 ]
Raznahan, Armin [1 ]
机构
[1] NIMH IRP, Sect Dev Neurogenom, Human Genet Branch, Bethesda, MD 20892 USA
[2] NIA IRP, Computat & Evolutionary Neurogenom Unit, Lab Neurogenet, NIH, Bethesda, MD 20892 USA
[3] NIMH IRP, Data Sci & Sharing Team, NIH, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
R-PACKAGE; EXPRESSION; SEQUENCE; AUTISM; INACTIVATION; ASSOCIATION; DISEASE; STRATA; NUMBER; REGION;
D O I
10.1038/s41559-024-02627-x
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Sex chromosomes are a fundamental aspect of sex-biased biology, but the extent to which homologous X-Y gene pairs ('the gametologs') contribute to sex-biased phenotypes remains hotly debated. Although these genes tend to exhibit large sex differences in expression throughout the body (XX females can express both X members, and XY males can express one X and one Y member), there is conflicting evidence regarding the degree of functional divergence between the X and Y members. Here we develop and apply co-expression fingerprint analysis to characterize functional divergence between the X and Y members of 17 gametolog gene pairs across >40 human tissues. Gametolog pairs exhibit functional divergence between the sexes that is driven by divergence between the X versus Y members (assayed in males), and this within-pair divergence is greatest among pairs with evolutionarily distant X and Y members. These patterns reflect that X versus Y gametologs show coordinated patterns of asymmetric coupling with large sets of autosomal genes, which are enriched for functional pathways and gene sets implicated in sex-biased biology and disease. Our findings suggest that the X versus Y gametologs have diverged in function and prioritize specific gametolog pairs for future targeted experimental studies.
引用
收藏
页码:448 / 463
页数:35
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