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逆转录病毒逆转录酶对正链引物的选择、去除及再利用分析。

Analysis of plus-strand primer selection, removal, and reutilization by retroviral reverse transcriptases.

作者信息

Schultz S J, Zhang M, Kelleher C D, Champoux J J

机构信息

Department of Microbiology, School of Medicine, University of Washington, Seattle, Washington 98195-7242, USA.

出版信息

J Biol Chem. 2000 Oct 13;275(41):32299-309. doi: 10.1074/jbc.M000021200.

Abstract

The ability of reverse transcriptase to generate, extend, and remove the primer derived from the polypurine tract (PPT) is vital for reverse transcription, since this process determines one of the ends required for integration of the viral DNA. Based on the ability of the RNase H activity of Moloney murine leukemia virus reverse transcriptase to cleave a long RNA/DNA hybrid containing the PPT, it appears that cleavages that could generate the plus-strand primer can occur by an internal cleavage mechanism without any positioning by an RNA 5'-end, and such cleavages may serve to minimize cleavage events within the PPT itself. If the PPT were to be cleaved inappropriately just upstream of the normal plus-strand origin site, the resulting 3'-ends would not be extended by reverse transcriptase. Extension of the PPT primer by at least 2 nucleotides is sufficient for recognition and correct cleavage by RNase H at the RNA-DNA junction to remove the primer. Specific removal of the PPT primer after polymerase extension deviates from the general observation that primer removal occurs by cleavage one nucleotide away from the RNA-DNA junction and suggests that the same PPT specificity determinants responsible for generation of the PPT primer also direct PPT primer removal. Once the PPT primer has been extended and removed from the nascent plus-strand DNA, reinitiation at the resulting plus-strand primer terminus does not occur, providing a mechanism to prevent the repeated initiation of plus strands.

摘要

逆转录酶生成、延伸和去除源自多聚嘌呤序列(PPT)的引物的能力对于逆转录至关重要,因为这一过程决定了病毒DNA整合所需的一端。基于莫洛尼鼠白血病病毒逆转录酶的核糖核酸酶H活性切割包含PPT的长RNA/DNA杂交体的能力,似乎产生正链引物的切割可通过内部切割机制发生,而无需RNA 5′端定位,并且这种切割可能有助于使PPT自身内部的切割事件最小化。如果PPT在正常正链起始位点上游被不恰当地切割,产生的3′端将不会被逆转录酶延伸。将PPT引物延伸至少2个核苷酸足以被核糖核酸酶H在RNA-DNA连接处识别并正确切割以去除引物。聚合酶延伸后PPT引物的特异性去除偏离了引物通过从RNA-DNA连接处切割一个核苷酸来去除的一般观察结果,这表明负责生成PPT引物的相同PPT特异性决定因素也指导PPT引物的去除。一旦PPT引物从新生的正链DNA上延伸并去除,在所得正链引物末端不会重新起始,从而提供了一种防止正链重复起始的机制。

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