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人类免疫缺陷病毒和鼠白血病病毒逆转录酶的保真度,由错配延伸频率表现出来,是序列依赖性的且与酶相关。

The fidelity of the reverse transcriptases of human immunodeficiency viruses and murine leukemia virus, exhibited by the mispair extension frequencies, is sequence dependent and enzyme related.

作者信息

Bakhanashvili M, Hizi A

机构信息

Department of Cell Biology and Histology, Sackler School of Medicine, Tel Aviv University, Israel.

出版信息

FEBS Lett. 1993 Mar 15;319(1-2):201-5. doi: 10.1016/0014-5793(93)80067-5.

DOI:10.1016/0014-5793(93)80067-5
PMID:7681015
Abstract

Sequence variations in HIV-1 and HIV-2 probably result in part from inaccurate DNA synthesis by viral reverse transcriptases (RTs). We have studied in vitro the fidelity of both the DNA- and RNA-dependent DNA polymerization functions of the two HIV RTs, as compared to that of murine leukemia virus (MLV) RT. The two HIV RTs were less accurate than MLV RT. The mispair extension frequencies observed previously with ribosomal RNA (rRNA) template were higher than those detected with phi X174am3 DNA template with all three RTs. In the current study we have investigated whether the nature of the copied nucleic acid (RNA vs. DNA) or the template nucleotide sequences affect the accuracy of DNA synthesis. We have analyzed the fidelity of DNA synthesis with DNA sequences identical to those of the rRNA sequences previously employed for reverse transcription. The results indicate that the fidelity of DNA synthesis depends mainly on the nucleotide sequences copied by every given RT. Yet, fidelity of DNA synthesis depends not only on the sequences copied but also on the nature of the enzymes per se. It is possible that these factors are major contributors to the high mutation rates of the two human immunodeficiency viruses.

摘要

HIV-1和HIV-2中的序列变异可能部分源于病毒逆转录酶(RTs)进行的不准确DNA合成。与鼠白血病病毒(MLV)RT相比,我们在体外研究了两种HIV RT的DNA依赖性和RNA依赖性DNA聚合功能的保真度。两种HIV RT的准确性均低于MLV RT。以前用核糖体RNA(rRNA)模板观察到的错配延伸频率高于用phi X174am3 DNA模板检测到的所有三种RT的错配延伸频率。在当前研究中,我们调查了被复制核酸的性质(RNA与DNA)或模板核苷酸序列是否会影响DNA合成的准确性。我们用与先前用于逆转录的rRNA序列相同的DNA序列分析了DNA合成的保真度。结果表明,DNA合成的保真度主要取决于每个给定RT复制的核苷酸序列。然而,DNA合成的保真度不仅取决于复制的序列,还取决于酶本身的性质。这些因素可能是两种人类免疫缺陷病毒高突变率的主要原因。

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