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人类核心启动子超长串联重复序列的进化趋势。

Evolutionary trend of exceptionally long human core promoter short tandem repeats.

机构信息

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

出版信息

Gene. 2012 Oct 1;507(1):61-7. doi: 10.1016/j.gene.2012.07.001. Epub 2012 Jul 13.

Abstract

Short tandem repeats (STRs) are variable elements that play a significant role in genome evolution by creating and maintaining quantitative genetic variation. Because of their proximity to the +1 transcription start site (TSS) and polymorphic nature, core promoter STRs may be considered a novel source of variation across species. In a genome-scale analysis of the entire human protein-coding genes annotated in the GeneCards database (19,927), we analyze the prevalence and repeat numbers of different classes of core promoter STRs in the interval between -120 and +1 to the TSS. We also analyze the evolutionary trend of exceptionally long core promoter STRs of ≥6-repeats. 133 genes (~2%) had core promoter STRs of ≥6-repeats. In the majority of those genes, the STR motifs were found to be conserved across evolution. Di-nucleotide repeats had the highest representation in the human core promoter long STRs (72 genes). Tri- (52 genes), tetra-, penta-, and hexa-nucleotide STRs (9 genes) were also present in the descending prevalence. The majority of those genes (84 genes) revealed directional expansion of core promoter STRs from mouse to human. However, in a number of genes, the difference in average allele size across species was sufficiently small that there might be a constraint on the evolution of average allele size. Random drift of STRs from mouse to human was also observed in a minority of genes. Future work on the genes listed in the current study may further our knowledge into the potential importance of core promoter STRs in human evolution.

摘要

短串联重复序列(STRs)是可变元件,通过创造和维持数量遗传变异在基因组进化中起着重要作用。由于它们靠近+1 转录起始位点(TSS)和多态性,核心启动子 STR 可以被认为是物种间变异的新来源。在对 GeneCards 数据库(19927 个)中注释的人类全部蛋白编码基因进行的全基因组分析中,我们分析了-120 到+1 之间 TSS 间隔内不同类别核心启动子 STR 的出现率和重复数。我们还分析了长度≥6 个重复的异常长核心启动子 STR 的进化趋势。133 个基因(约 2%)具有≥6 个重复的核心启动子 STR。在大多数基因中,STR 基序在进化中被发现是保守的。二核苷酸重复在人类核心启动子长 STR 中具有最高的代表性(72 个基因)。三核苷酸(52 个基因)、四核苷酸、五核苷酸和六核苷酸 STR(9 个基因)也以递减的流行率存在。这些基因中的大多数(84 个基因)显示核心启动子 STR 从老鼠到人类的定向扩张。然而,在一些基因中,物种间平均等位基因大小的差异足够小,以至于平均等位基因大小的进化可能受到限制。少数基因也观察到 STR 从老鼠到人类的随机漂移。对当前研究中列出的基因的进一步研究可能会进一步了解核心启动子 STR 在人类进化中的潜在重要性。

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