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DNA碱基组成的进化模式及其与DNA修复系统多态性的相关性

Evolutionary patterns of DNA base composition and correlation to polymorphisms in DNA repair systems.

作者信息

Li Xianran, Scanlon Michael J, Yu Jianming

机构信息

Department of Agronomy, Iowa State University, Ames, IA 50011, USA.

Plant Biology Section, School of Integrative Plant Science, Cornell University, Ithaca, NY 14853, USA.

出版信息

Nucleic Acids Res. 2015 Apr 20;43(7):3614-25. doi: 10.1093/nar/gkv197. Epub 2015 Mar 12.

Abstract

DNA base composition is a fundamental genome feature. However, the evolutionary pattern of base composition and its potential causes have not been well understood. Here, we report findings from comparative analysis of base composition at the whole-genome level across 2210 species, the polymorphic-site level across eight population comparison sets, and the mutation-site level in 12 mutation-tracking experiments. We first demonstrate that base composition follows the individual-strand base equality rule at the genome, chromosome and polymorphic-site levels. More intriguingly, clear separation of base-composition values calculated across polymorphic sites was consistently observed between basal and derived groups, suggesting common underlying mechanisms. Individuals in the derived groups show an A&T-increase/G&C-decrease pattern compared with the basal groups. Spontaneous and induced mutation experiments indicated these patterns of base composition change can emerge across mutation sites. With base-composition across polymorphic sites as a genome phenotype, genome scans with human 1000 Genomes and HapMap3 data identified a set of significant genomic regions enriched with Gene Ontology terms for DNA repair. For three DNA repair genes (BRIP1, PMS2P3 and TTDN), ENCODE data provided evidence for interaction between genomic regions containing these genes and regions containing the significant SNPs. Our findings provide insights into the mechanisms of genome evolution.

摘要

DNA碱基组成是一种基本的基因组特征。然而,碱基组成的进化模式及其潜在原因尚未得到很好的理解。在此,我们报告了在全基因组水平上对2210个物种、在八个群体比较组的多态性位点水平以及在12个突变追踪实验中的突变位点水平进行碱基组成比较分析的结果。我们首先证明,在基因组、染色体和多态性位点水平上,碱基组成遵循单链碱基平等规则。更有趣的是,在基部类群和衍生类群之间,始终观察到跨多态性位点计算的碱基组成值有明显分离,这表明存在共同的潜在机制。与基部类群相比,衍生类群中的个体呈现出A&T增加/G&C减少的模式。自发和诱导突变实验表明,这些碱基组成变化模式可以在突变位点出现。以跨多态性位点的碱基组成为一种基因组表型,利用人类千人基因组计划和HapMap3数据进行的基因组扫描识别出一组富含DNA修复基因本体术语的显著基因组区域。对于三个DNA修复基因(BRIP1、PMS2P3和TTDN),ENCODE数据提供了证据,证明含有这些基因的基因组区域与含有显著单核苷酸多态性的区域之间存在相互作用。我们的研究结果为基因组进化机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3562/4402523/b2cd20262fd4/gkv197fig1.jpg

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