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性染色体编码蛋白同源物:当前的进展和未解决的问题。

Sex chromosome-encoded protein homologs: current progress and open questions.

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA, USA.

Graduate Group in Biochemistry and Molecular Biophysics, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Nat Struct Mol Biol. 2024 Aug;31(8):1156-1166. doi: 10.1038/s41594-024-01362-y. Epub 2024 Aug 9.

Abstract

The complexity of biological sex differences is markedly evident in human physiology and pathology. Although many of these differences can be ascribed to the expression of sex hormones, another contributor to sex differences lies in the sex chromosomes beyond their role in sex determination. Although largely nonhomologous, the human sex chromosomes express seventeen pairs of homologous genes, referred to as the 'X-Y pairs.' The X chromosome-encoded homologs of these Y-encoded proteins are crucial players in several cellular processes, and their dysregulation frequently results in disease development. Many diseases related to these X-encoded homologs present with sex-biased incidence or severity. By contrast, comparatively little is known about the differential functions of the Y-linked homologs. Here, we summarize and discuss the current understanding of five of these X-Y paired proteins, with recent evidence of differential functions and of having a potential link to sex biases in disease, highlighting how amino acid-level sequence differences may differentiate their functions and contribute to sex biases in human disease.

摘要

生物性别差异的复杂性在人类生理学和病理学中表现得非常明显。尽管这些差异中的许多可以归因于性激素的表达,但性别差异的另一个贡献在于性染色体超出其性别决定作用之外。尽管在很大程度上是非同源的,但人类性染色体表达十七对同源基因,称为“X-Y 对”。这些 Y 编码蛋白的 X 染色体编码同源物是几个细胞过程中的关键参与者,它们的失调经常导致疾病的发展。许多与这些 X 编码同源物相关的疾病表现出性别偏向的发病率或严重程度。相比之下,关于 Y 连锁同源物的差异功能知之甚少。在这里,我们总结和讨论了目前对其中五个 X-Y 配对蛋白的理解,最近有证据表明它们具有不同的功能,并可能与疾病中的性别偏见有关,强调了氨基酸水平序列差异如何区分它们的功能,并导致人类疾病中的性别偏见。

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