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首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Construction of PRDM9 allele-specific recombination maps in cattle using large-scale pedigree analysis and genome-wide single sperm genomics
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Construction of PRDM9 allele-specific recombination maps in cattle using large-scale pedigree analysis and genome-wide single sperm genomics

机译:使用大规模谱系分析和基因组的单一精子基因组学中PRDM9等位基因特异性重组图的构建

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摘要

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 hot-spot 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.
机译:PRDM9有助于杂交无菌和物种演化。但是,它的作用是在牛,是一个主要的驯养物种的牛。我们之前发现PRDM9附近的关联,牛重组功能,但致病变体仍然未知。使用数百万基因分型牛与血统信息,我们为五个PRDM9等位基因和生成的等位基因特异性重组图谱。通过检查特定的等位基因的重组模式,我们观察了PRDM9对重组全球分布的影响,特别是在染色体的两端。我们还展示了重组热点区域和PRDM9锌指域内的功能突变之间的强烈关联。更重要的是,我们发现PRDM9的一位等位基因与蛋白质组成和重组景观中的其他等位基因非常不同,表明该等位基因对PRDM9和牛重组之间的关系的致病作用。当从精子和谱系数据中比较重组图时,我们观察到类似的基因组重组模式,验证基于谱系的结果的质量。总的来说,这些证据支持PRDM9等位基因作为报告与牛重组联系的因果变量。我们的研究全面调查了牛PRDM9等位基因,产生了等位基因特异性的重组图,并扩大了我们对PRDM9对重组基因组分布的作用的理解。

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