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在高重组区域,人类单核苷酸多态性(SNP)的变异性和突变率更高。

Human SNP variability and mutation rate are higher in regions of high recombination.

作者信息

Lercher Martin J, Hurst Laurence D

机构信息

Dept of Biology and Biochemistry, University of Bath, BA2 7AY., Bath, UK.

出版信息

Trends Genet. 2002 Jul;18(7):337-40. doi: 10.1016/s0168-9525(02)02669-0.

Abstract

Understanding the co-variation of nucleotide diversity and local recombination rates is important both for the mapping of disease-associated loci and in understanding the causes of sequence evolution. It is known that single nucleotide polymorphisms (SNPs) around protein coding genes show higher diversity in regions of high recombination. Here, we find that this correlation holds for SNPs across the entire human genome, the great majority of which are not near exons or control elements. Contrasting with results from coding regions, we provide evidence that the higher nucleotide diversity in regions of high recombination is most likely due, at least in part, to a higher mutation rate. One possible explanation for this is that recombination is mutagenic.

摘要

了解核苷酸多样性与局部重组率的共同变化,对于疾病相关位点的定位以及理解序列进化的原因都非常重要。众所周知,蛋白质编码基因周围的单核苷酸多态性(SNP)在高重组区域表现出更高的多样性。在此,我们发现这种相关性在整个人类基因组的SNP中都成立,其中绝大多数SNP并不靠近外显子或调控元件。与编码区域的结果相反,我们提供的证据表明,高重组区域中较高的核苷酸多样性很可能至少部分是由于较高的突变率。对此一种可能的解释是重组具有诱变作用。

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