Rigby Sean T, Van Nostrand Keith P, Rose April E, Gorelick Robert J, Mathews David H, Bambara Robert A
Department of Biochemistry and Biophysics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
J Mol Biol. 2009 Dec 11;394(4):694-707. doi: 10.1016/j.jmb.2009.10.036. Epub 2009 Oct 21.
Human immunodeficiency virus-1 employs strand transfer for recombination between two viral genomes. We have previously provided evidence that strand transfer proceeds by an invasion-mediated mechanism in which a DNA segment on the original RNA template is invaded by a second RNA template at a gap site. The initial RNA-DNA hybrid then expands until the DNA is fully transferred. Ribonuclease H (RNase H) cleavages and nucleocapsid protein (NC) were required for long-distance propagation of the hybrid. Evaluation was performed on a unique substrate, with a short gap serving as a precreated invasion site. In our current work, this substrate provided an opportunity for us to test what factors influence a specific invasion site to support transfer, and to distinguish factors that influence invasion site creation from those that impact later steps. RNase H can act in a polymerization-dependent or polymerization-independent mode. Polymerization-dependent and polymerization-independent RNase H were found to be important in creating efficiently used invasion sites in the primer-donor complex, with or without NC. Propagation and terminus transfer steps, emanating from a precreated invasion site in the presence of NC, were stimulated by polymerization-dependent, but not polymerization-independent, RNase H. RNase H can carry out primary and secondary cleavages during synthesis. While both modes of cleavage promoted invasion, only primary cleavage promoted propagation in the presence of NC in our system. These observations suggest that once invasion is initiated at a short gap, it can propagate through an adjacent region interrupted only by nicks, with help by NC. We considered the possibility that propagation solely by strand exchange was a significant contributor to transfers. However, it did not promote transfer even if synthetic progress of reverse transcriptase was intentionally slowed, consistent with strand exchange by random walk in which rate declines precipitously with distance.
人类免疫缺陷病毒1型利用链转移实现两个病毒基因组之间的重组。我们之前已提供证据表明,链转移通过一种入侵介导的机制进行,即原始RNA模板上的一个DNA片段在一个缺口位点被第二个RNA模板入侵。最初的RNA-DNA杂交体随后扩展,直到DNA完全转移。杂交体的长距离延伸需要核糖核酸酶H(RNase H)切割和核衣壳蛋白(NC)。评估是在一种独特的底物上进行的,该底物有一个短缺口作为预先形成的入侵位点。在我们目前的工作中,这种底物为我们提供了一个机会,来测试哪些因素影响特定的入侵位点以支持转移,并区分影响入侵位点形成的因素和影响后续步骤的因素。RNase H可以以聚合依赖性或聚合非依赖性模式发挥作用。发现聚合依赖性和聚合非依赖性RNase H在引物-供体复合物中高效利用的入侵位点的形成中很重要,无论有无NC。在有NC的情况下,从预先形成的入侵位点开始的延伸和末端转移步骤受到聚合依赖性RNase H的刺激,但不受聚合非依赖性RNase H的刺激。RNase H在合成过程中可以进行一级和二级切割。虽然两种切割模式都促进了入侵,但在我们的系统中,只有一级切割在有NC的情况下促进了延伸。这些观察结果表明,一旦在短缺口处启动入侵,在NC的帮助下,它可以通过仅被切口中断的相邻区域进行延伸。我们考虑了仅通过链交换进行延伸对转移有重大贡献的可能性。然而,即使故意减缓逆转录酶的合成进程,它也不会促进转移,这与随机游走的链交换一致,即速率随距离急剧下降。