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利用大规模家系分析和全基因组单精子基因组学构建牛 PRDM9 等位基因特异性重组图谱。

Construction of PRDM9 allele-specific recombination maps in cattle using large-scale pedigree analysis and genome-wide single sperm genomics.

机构信息

Animal Genomics and Improvement Laboratory, BARC, USDA-ARS, Beltsville, MD 20705, USA.

Shaanxi Key Laboratory of Agricultural Molecular Biology, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi 712100, China.

出版信息

DNA Res. 2018 Apr 1;25(2):183-194. doi: 10.1093/dnares/dsx048.

Abstract

PRDM9 contributes to hybrid sterility and species evolution. However, its role is to be confirmed in cattle, a major domesticated livestock species. We previously found an association near PRDM9 with cattle recombination features, but the causative variants are still unknown. Using millions of genotyped cattle with pedigree information, we characterized five PRDM9 alleles and generated allele-specific recombination maps. By examining allele-specific recombination patterns, we observed the impact of PRDM9 on global distribution of recombination, especially in the two ends of chromosomes. We also showed strong associations between recombination hotspot regions and functional mutations within PRDM9 zinc finger domain. More importantly, we found one allele of PRDM9 to be very different from others in both protein composition and recombination landscape, indicating the causative role of this allele on the association between PRDM9 and cattle recombination. When comparing recombination maps from sperm and pedigree data, we observed similar genome-wide recombination patterns, validating the quality of pedigree-based results. Collectively, these evidence supported PRDM9 alleles as causal variants for the reported association with cattle recombination. Our study comprehensively surveyed the bovine PRDM9 alleles, generated allele-specific recombination maps, and expanded our understanding of the role of PRDM9 on genome distribution of recombination.

摘要

PRDM9 有助于杂种不育和物种进化。然而,其在牛(一种主要的家畜物种)中的作用尚待证实。我们之前在 PRDM9 附近发现了与牛重组特征相关的关联,但致病变体仍不清楚。利用具有系谱信息的数百万个基因分型牛,我们对 5 个 PRDM9 等位基因进行了特征描述,并生成了等位基因特异性重组图谱。通过检查等位基因特异性重组模式,我们观察到 PRDM9 对重组全球分布的影响,特别是在染色体的两端。我们还显示了重组热点区域与 PRDM9 锌指结构域内功能突变之间的强烈关联。更重要的是,我们发现 PRDM9 的一个等位基因在蛋白质组成和重组景观方面与其他等位基因非常不同,表明该等位基因在 PRDM9 与牛重组之间的关联中起致病作用。当比较来自精子和系谱数据的重组图谱时,我们观察到类似的全基因组重组模式,验证了基于系谱的结果的质量。总之,这些证据支持 PRDM9 等位基因作为与牛重组相关报道的致病变体。我们的研究全面调查了牛的 PRDM9 等位基因,生成了等位基因特异性重组图谱,并扩展了我们对 PRDM9 对重组基因组分布的作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ca/5909443/f40854b74d61/dsx048f1.jpg

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