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HIV-1第二链转移反应的体外分析

In vitro analysis of the HIV-1 second strand-transfer reaction.

作者信息

Pop M P

机构信息

Department of Biochemical Kinetics, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany.

出版信息

Biochim Biophys Acta. 1996 Jun 7;1307(2):193-204. doi: 10.1016/0167-4781(96)00043-7.

Abstract

Two strand-transfer reactions are required during the retroviral reverse transcription. The second strand-transfer is believed to occur at the primer binding site (PBS). By using an in vitro model system derived from the human immunodeficiency virus type-1 (HIV-1), molecular events related to the second strand-transfer reaction were examined. The RNA-directed DNA synthesis catalyzed by the HIV-1 reverse transcriptase (RT) appears to pause twice, around the 2nd and the 11th bases downstream into the HIV-1 PBS. In either case, pausing seems to be caused by local sequence effects. From both these pause sites the nascent DNA strands can undergo transfer to PBS-homologous templates. The results confirm that pausing favors the internal strand-transfer. They also indicate that PBS-mediated transfers proceed through displacement of the DNA strands from RNA donor molecules by the acceptor template, as in one of the models proposed by DeStefano et al. (DeStefano, J.J., Bambara, R.A. and Fay, P.J. (1994) J. Biol. Chem. 269, 161-168). Whereas no hydrolysis by the ribonuclease H activity of HIV-1 RT seemed to occur within the HIV-1 PBS, specific cleavage was observed outside of this sequence and noticeably 5 bases upstream from its 3' end relative to the DNA primer growing point. This particular cleavage event remained essentially unchanged when the second pause site downstream into the PBS, located 16 bases beyond, was removed by mutation. The experiments suggest that this prominent RNA degradation event could precede the PBS-mediated strand-transfers.

摘要

逆转录病毒逆转录过程需要两个链转移反应。据信第二个链转移发生在引物结合位点(PBS)。通过使用源自人类免疫缺陷病毒1型(HIV-1)的体外模型系统,研究了与第二个链转移反应相关的分子事件。HIV-1逆转录酶(RT)催化的RNA指导的DNA合成似乎会在进入HIV-1 PBS下游的第2个和第11个碱基左右停顿两次。在这两种情况下,停顿似乎都是由局部序列效应引起的。从这两个停顿位点开始,新生的DNA链都可以转移到与PBS同源的模板上。结果证实停顿有利于内部链转移。它们还表明,PBS介导的转移是通过受体模板将DNA链从RNA供体分子上置换下来进行的,正如DeStefano等人提出的模型之一(DeStefano, J.J., Bambara, R.A.和Fay, P.J. (1994) J. Biol. Chem. 269, 161 - 168)。虽然HIV-1 RT的核糖核酸酶H活性在HIV-1 PBS内似乎没有发生水解,但在该序列之外且相对于DNA引物生长点在其3'端上游明显5个碱基处观察到了特异性切割。当通过突变去除PBS下游16个碱基处第二个停顿位点时,这种特定的切割事件基本保持不变。实验表明,这种显著的RNA降解事件可能先于PBS介导的链转移。

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