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人类内源性逆转录病毒家族HERV-K(HML-5):人类基因组中一种古老β逆转录病毒的现状、进化与重建

Human endogenous retrovirus family HERV-K(HML-5): status, evolution, and reconstruction of an ancient betaretrovirus in the human genome.

作者信息

Lavie Laurence, Medstrand Patrik, Schempp Werner, Meese Eckart, Mayer Jens

机构信息

Department of Human Genetics, Building 60, University of Saarland, Medical Faculty, 66421 Homburg, Germany.

出版信息

J Virol. 2004 Aug;78(16):8788-98. doi: 10.1128/JVI.78.16.8788-8798.2004.

Abstract

The human genome harbors numerous distinct families of so-called human endogenous retroviruses (HERV) which are remnants of exogenous retroviruses that entered the germ line millions of years ago. We describe here the hitherto little-characterized betaretrovirus HERV-K(HML-5) family (named HERVK22 in Repbase) in greater detail. Out of 139 proviruses, only a few loci represent full-length proviruses, and many lack gag protease and/or env gene regions. We generated a consensus sequence from multiple alignment of 62 HML-5 loci that displays open reading frames for the four major retroviral proteins. Four HML-5 long terminal repeat (LTR) subfamilies were identified that are associated with monophyletic proviral bodies, implying different evolution of HML-5 LTRs and genes. Sequence analysis indicated that the proviruses formed approximately 55 million years ago. Accordingly, HML-5 proviral sequences were detected in Old World and New World primates but not in prosimians. No recent activity is associated with this HERV family. We also conclude that the HML-5 consensus sequence primer binding site is identical to methionine tRNA. Therefore, the family should be designated HERV-M. Our study provides important insights into the structure and evolution of the oldest betaretrovirus in the primate genome known to date.

摘要

人类基因组中存在众多不同的所谓人类内源性逆转录病毒(HERV)家族,它们是数百万年前进入种系的外源性逆转录病毒的残余物。我们在此更详细地描述了迄今特征较少的β逆转录病毒HERV-K(HML-5)家族(在Repbase中命名为HERVK22)。在139个前病毒中,只有少数位点代表全长前病毒,许多缺乏gag蛋白酶和/或env基因区域。我们通过对62个HML-5位点的多序列比对生成了一个共有序列,该序列显示了四种主要逆转录病毒蛋白的开放阅读框。鉴定出四个HML-5长末端重复序列(LTR)亚家族,它们与单系前病毒体相关,这意味着HML-5 LTR和基因的进化不同。序列分析表明,前病毒大约在5500万年前形成。因此,在旧世界和新世界灵长类动物中检测到了HML-5前病毒序列,但在原猴亚目中未检测到。这个HERV家族没有近期的活性。我们还得出结论,HML-5共有序列引物结合位点与甲硫氨酸tRNA相同。因此,该家族应命名为HERV-M。我们的研究为迄今为止已知的灵长类基因组中最古老的β逆转录病毒的结构和进化提供了重要见解。

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