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野生小鼠中Prdm9锌指阵列的多样性揭示了这种编码微卫星进化更替的新方面。

Diversity of Prdm9 zinc finger array in wild mice unravels new facets of the evolutionary turnover of this coding minisatellite.

作者信息

Buard Jérôme, Rivals Eric, Dunoyer de Segonzac Denis, Garres Charlotte, Caminade Pierre, de Massy Bernard, Boursot Pierre

机构信息

Institute of Human Genetics, UPR 1142, Centre National de la Recherche Scientifique, Montpellier, France.

Laboratoire d'Informatique, de Robotique et de Microélectronique de Montpellier, UMR 5506, Université Montpellier 2, Centre National de la Recherche Scientifique, Montpellier, France ; Institut de Biologie Computationnelle, Montpellier, France.

出版信息

PLoS One. 2014 Jan 13;9(1):e85021. doi: 10.1371/journal.pone.0085021. eCollection 2014.

Abstract

In humans and mice, meiotic recombination events cluster into narrow hotspots whose genomic positions are defined by the PRDM9 protein via its DNA binding domain constituted of an array of zinc fingers (ZnFs). High polymorphism and rapid divergence of the Prdm9 gene ZnF domain appear to involve positive selection at DNA-recognition amino-acid positions, but the nature of the underlying evolutionary pressures remains a puzzle. Here we explore the variability of the Prdm9 ZnF array in wild mice, and uncovered a high allelic diversity of both ZnF copy number and identity with the caracterization of 113 alleles. We analyze features of the diversity of ZnF identity which is mostly due to non-synonymous changes at codons -1, 3 and 6 of each ZnF, corresponding to amino-acids involved in DNA binding. Using methods adapted to the minisatellite structure of the ZnF array, we infer a phylogenetic tree of these alleles. We find the sister species Mus spicilegus and M. macedonicus as well as the three house mouse (Mus musculus) subspecies to be polyphyletic. However some sublineages have expanded independently in Mus musculus musculus and M. m. domesticus, the latter further showing phylogeographic substructure. Compared to random genomic regions and non-coding minisatellites, none of these patterns appears exceptional. In silico prediction of DNA binding sites for each allele, overlap of their alignments to the genome and relative coverage of the different families of interspersed repeated elements suggest a large diversity between PRDM9 variants with a potential for highly divergent distributions of recombination events in the genome with little correlation to evolutionary distance. By compiling PRDM9 ZnF protein sequences in Primates, Muridae and Equids, we find different diversity patterns among the three amino-acids most critical for the DNA-recognition function, suggesting different diversification timescales.

摘要

在人类和小鼠中,减数分裂重组事件聚集在狭窄的热点区域,其基因组位置由PRDM9蛋白通过其由一系列锌指(ZnF)构成的DNA结合结构域来定义。Prdm9基因锌指结构域的高度多态性和快速分化似乎涉及DNA识别氨基酸位置的正选择,但其潜在进化压力的本质仍然是个谜。在这里,我们探索了野生小鼠中Prdm9锌指阵列的变异性,并通过对113个等位基因的表征揭示了锌指拷贝数和同一性的高度等位基因多样性。我们分析了锌指同一性多样性的特征,这主要是由于每个锌指密码子-1、3和6处的非同义变化,这些密码子对应于参与DNA结合的氨基酸。使用适用于锌指阵列微卫星结构的方法,我们推断了这些等位基因的系统发育树。我们发现姐妹物种小家鼠和马其顿小家鼠以及三个家鼠(小家鼠)亚种是多系的。然而,一些亚谱系在小家鼠和小家鼠指名亚种中独立扩展,后者进一步显示出系统地理亚结构。与随机基因组区域和非编码微卫星相比,这些模式都没有异常。对每个等位基因的DNA结合位点进行计算机预测、它们与基因组比对的重叠以及散布重复元件不同家族的相对覆盖表明,PRDM9变体之间存在很大差异,基因组中重组事件的分布可能高度不同,且与进化距离几乎没有相关性。通过汇编灵长类动物、鼠科动物和马科动物中的PRDM9锌指蛋白序列,我们发现在对DNA识别功能最关键的三个氨基酸之间存在不同的多样性模式,这表明存在不同的多样化时间尺度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67ea/3890296/b8b7cf3f8f73/pone.0085021.g001.jpg

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