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补体成分C4基因内含子9作为灵长类动物的系统发育标记:内源性逆转录病毒ERV-K(C4)的长末端重复序列是进化的分子时钟。

Complement component C4 gene intron 9 as a phylogenetic marker for primates: long terminal repeats of the endogenous retrovirus ERV-K(C4) are a molecular clock of evolution.

作者信息

Dangel A W, Baker B J, Mendoza A R, Yu C Y

机构信息

Children's Hospital Research Foundation, Columbus, OH 43205, USA.

出版信息

Immunogenetics. 1995;42(1):41-52. doi: 10.1007/BF00164986.

DOI:10.1007/BF00164986
PMID:7797267
Abstract

The complement component C4 genes of Old World primates exhibit a long/short dichotomous size variation, except that chimpanzee and gorilla only contain short C4 genes. In human it has been shown that the long C4 gene is attributed to the integration of an endogenous retrovirus, HERV-K(C4), into intron 9. This 6.36 kilobase retroviral element is absent in short C4 genes. Here it is shown that the homologous endogenous retrovirus, ERV-K(C4), is present precisely at the same position in the long C4 gene of orangutan and African green monkey. Determination of the short C4 gene intron 9 sequences from human, three apes, two Old World monkeys, and a New World monkey allowed the establishment of consistent phylogenetic trees for primates, which favors a chimpanzee-gorilla clade. The 5' long terminal repeats (LTR) and 3' LTR of ERV-K(C4) in long C4 genes of human, orangutan, and African green monkey have similar sequence divergence values of 9.1%-10.5%. These values are more than five-fold higher than the sequence divergence of the homologous intron 9 sequences between the long and short C4 genes in higher primates. The latter is probably a result of homogenization or concerted evolution. We suggest that the 5' LTR and 3' LTR of an endogenous retrovirus can serve as a reliable reference point or a molecular clock for studies of gene duplication and gene evolution. This is because the 5'/3' LTR sequences were identical at the time of retroviral integration and evolved independently of each other afterwards. Our data provides strong evidence for the short C4 gene being the ancestral form in primates, trans-species evolution, and the "slow-down" phenomenon of the sequence divergence in great apes.

摘要

旧世界灵长类动物的补体成分C4基因呈现出长/短二分法的大小变异,不过黑猩猩和大猩猩只含有短C4基因。在人类中,已经表明长C4基因归因于一种内源性逆转录病毒HERV-K(C4)整合到内含子9中。这个6.36千碱基的逆转录病毒元件在短C4基因中不存在。在这里表明,同源内源性逆转录病毒ERV-K(C4)恰好在猩猩和非洲绿猴的长C4基因的相同位置存在。对人类、三种猿类、两种旧世界猴和一种新世界猴的短C4基因内含子9序列的测定,使得能够建立灵长类动物一致的系统发育树,这支持黑猩猩-大猩猩进化枝。人类、猩猩和非洲绿猴的长C4基因中ERV-K(C4)的5'长末端重复序列(LTR)和3'LTR具有相似的序列分歧值,为9.1%-10.5%。这些值比高等灵长类动物长C和短C4基因之间同源内含子9序列的序列分歧高五倍多。后者可能是均一化或协同进化的结果。我们认为,内源性逆转录病毒的5'LTR和3'LTR可以作为研究基因复制和基因进化的可靠参考点或分子时钟。这是因为5'/3'LTR序列在逆转录病毒整合时是相同的,并且之后彼此独立进化。我们的数据为短C4基因是灵长类动物的祖先形式、跨物种进化以及大猿中序列分歧的“减速”现象提供了有力证据。

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Immunogenetics. 1994;40(6):381-96. doi: 10.1007/BF00177822.
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