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人类假常染色体区域的进化动态。

Evolutionary dynamics of the human pseudoautosomal regions.

机构信息

Institute of Investigation and Innovation in Health (i3S). University of Porto, Porto, Portugal.

Institute of Molecular Pathology and Immunology (IPATIMUP), University of Porto, Porto, Portugal.

出版信息

PLoS Genet. 2021 Apr 19;17(4):e1009532. doi: 10.1371/journal.pgen.1009532. eCollection 2021 Apr.

Abstract

Recombination between the X and Y human sex chromosomes is limited to the two pseudoautosomal regions (PARs) that present quite distinct evolutionary origins. Despite the crucial importance for male meiosis, genetic diversity patterns and evolutionary dynamics of these regions are poorly understood. In the present study, we analyzed and compared the genetic diversity of the PAR regions using publicly available genomic sequences encompassing both PAR1 and PAR2. Comparisons were performed through allele diversities, linkage disequilibrium status and recombination frequencies within and between X and Y chromosomes. In agreement with previous studies, we confirmed the role of PAR1 as a male-specific recombination hotspot, but also observed similar characteristic patterns of diversity in both regions although male recombination occurs at PAR2 to a much lower extent (at least one recombination event at PAR1 and in ≈1% in normal male meioses at PAR2). Furthermore, we demonstrate that both PARs harbor significantly different allele frequencies between X and Y chromosomes, which could support that recombination is not sufficient to homogenize the pseudoautosomal gene pool or is counterbalanced by other evolutionary forces. Nevertheless, the observed patterns of diversity are not entirely explainable by sexually antagonistic selection. A better understanding of such processes requires new data from intergenerational transmission studies of PARs, which would be decisive on the elucidation of PARs evolution and their role in male-driven heterosomal aneuploidies.

摘要

X 和 Y 人类性染色体之间的重组仅限于两个具有明显不同进化起源的假常染色体区域 (PARs)。尽管这对减数分裂至关重要,但这些区域的遗传多样性模式和进化动态仍知之甚少。在本研究中,我们使用包含 PAR1 和 PAR2 的公开基因组序列分析和比较了 PAR 区域的遗传多样性。通过等位基因多样性、连锁不平衡状态以及 X 和 Y 染色体内部和之间的重组频率进行了比较。与之前的研究一致,我们证实了 PAR1 作为男性特异性重组热点的作用,但也观察到两个区域具有相似的多样性特征模式,尽管在 PAR2 中男性重组的程度要低得多(至少在 PAR1 中有一个重组事件,在正常男性减数分裂中约为 1% 在 PAR2 中)。此外,我们证明 PARs 在 X 和 Y 染色体之间具有显著不同的等位基因频率,这可能支持重组不足以使假常染色体基因库同质化,或者受到其他进化力量的平衡。然而,观察到的多样性模式并不能完全用性拮抗选择来解释。要更好地理解这些过程,需要来自 PAR 世代间传递研究的新数据,这对于阐明 PARs 的进化及其在男性驱动的异源非整倍体中的作用将是决定性的。

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