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在HIV-1 RNA逆转录过程中,核衣壳蛋白对病毒DNA从5'到3'链转移的反式激活作用。

Trans-activation of the 5' to 3' viral DNA strand transfer by nucleocapsid protein during reverse transcription of HIV1 RNA.

作者信息

Darlix J L, Vincent A, Gabus C, de Rocquigny H, Roques B

机构信息

LaboRetro INSERM, Ecole Normale Supérieure de Lyon, France.

出版信息

C R Acad Sci III. 1993 Aug;316(8):763-71.

PMID:7519118
Abstract

Two DNA strand transfer reactions take place during reverse transcription of the retroviral genome. The first transfer, that of the minus-strand strong stop DNA from the 5' end of the viral RNA to the 3' end, has been studied in vitro with two RNAs mimicking the 5' and 3' regions of the HIV1 genome and with nucleocapsid protein, NCp7, and reverse transcriptase. The results show that NCp7 strongly activates the 5' to 3' DNA strand transfer during reverse transcription while a basic peptide resembling NCp7 is inactive. Activation of the first transfer by several NCp7 derived peptides and the influence of the terminal redundancies (R) present at the 5' and 3' ends of HIV1 RNA were also examined. The first transfer is optimal in the presence of intact NCp7 and necessitates R on both the 5' and 3' RNAs. Sequencing of full length viral DNA products reveals approximately 40% misincorporations at the first nucleotide beyond the transfer point. If such base misincorporations occur during proviral DNA synthesis with possible homologous recombinations it may well contribute to the high level of genetic variability of HIV.

摘要

在逆转录病毒基因组的逆转录过程中发生了两个DNA链转移反应。第一次转移,即负链强终止DNA从病毒RNA的5'端转移到3'端,已经在体外使用模拟HIV-1基因组5'和3'区域的两种RNA以及核衣壳蛋白NCp7和逆转录酶进行了研究。结果表明,NCp7在逆转录过程中强烈激活5'到3'的DNA链转移,而一种类似NCp7的碱性肽则没有活性。还研究了几种源自NCp7的肽对第一次转移的激活作用以及HIV-1 RNA 5'和3'末端存在的末端冗余(R)的影响。在完整的NCp7存在下,第一次转移是最佳的,并且5'和3' RNA上都需要R。全长病毒DNA产物的测序显示,在转移点之后的第一个核苷酸处大约有40%的错误掺入。如果在原病毒DNA合成过程中发生这种碱基错误掺入并可能发生同源重组,那么它很可能导致HIV的高水平遗传变异性。

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