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灵长类动物中动态肌动蛋白基因家族的进化。

Dynamic actin gene family evolution in primates.

机构信息

Institute of System Biology, Shanghai University, Shanghai 200444, China.

出版信息

Biomed Res Int. 2013;2013:630803. doi: 10.1155/2013/630803. Epub 2013 Jun 6.

Abstract

Actin is one of the most highly conserved proteins and plays crucial roles in many vital cellular functions. In most eukaryotes, it is encoded by a multigene family. Although the actin gene family has been studied a lot, few investigators focus on the comparison of actin gene family in relative species. Here, the purpose of our study is to systematically investigate characteristics and evolutionary pattern of actin gene family in primates. We identified 233 actin genes in human, chimpanzee, gorilla, orangutan, gibbon, rhesus monkey, and marmoset genomes. Phylogenetic analysis showed that actin genes in the seven species could be divided into two major types of clades: orthologous group versus complex group. Codon usages and gene expression patterns of actin gene copies were highly consistent among the groups because of basic functions needed by the organisms, but much diverged within species due to functional diversification. Besides, many great potential pseudogenes were found with incomplete open reading frames due to frameshifts or early stop codons. These results implied that actin gene family in primates went through "birth and death" model of evolution process. Under this model, actin genes experienced strong negative selection and increased the functional complexity by reproducing themselves.

摘要

肌动蛋白是一种高度保守的蛋白质,在许多重要的细胞功能中发挥着关键作用。在大多数真核生物中,它由一个多基因家族编码。尽管肌动蛋白基因家族已经被研究了很多,但很少有研究人员关注相对物种中肌动蛋白基因家族的比较。在这里,我们研究的目的是系统地研究灵长类动物肌动蛋白基因家族的特征和进化模式。我们在人类、黑猩猩、大猩猩、猩猩、长臂猿、恒河猴和狨猴的基因组中鉴定出 233 个肌动蛋白基因。系统发育分析表明,这七种物种中的肌动蛋白基因可以分为两类主要的分支:同源群与复杂群。由于生物体的基本功能需要,肌动蛋白基因的密码子使用和基因表达模式在这些组中高度一致,但由于功能多样化,在种内却有很大的差异。此外,由于移码或早期终止密码子,许多具有不完全开放阅读框的潜在假基因也被发现。这些结果表明,灵长类动物的肌动蛋白基因家族经历了“诞生和死亡”的进化过程模型。在这个模型中,肌动蛋白基因经历了强烈的负选择,并通过自我复制增加了功能的复杂性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94ec/3690210/937f5797a26a/BMRI2013-630803.001.jpg

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