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首页> 外文期刊>Journal of Molecular Biology >The HIV plus-strand transfer reaction: determination of replication-competent intermediates and identification of a novel lentiviral element, the primer over-extension sequence.
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The HIV plus-strand transfer reaction: determination of replication-competent intermediates and identification of a novel lentiviral element, the primer over-extension sequence.

机译:HIV加链转移反应:确定具有复制能力的中间体,并鉴定新的慢病毒元件,即引物过度延伸序列。

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Current retroviral replication models propose that during (+) strand synthesis, the initial (-) strand tRNA primer is partially replicated to reproduce the 18 nt primer-binding site (PBS). Subsequent removal of the tRNA primer from the (-) strand template exposes the PBS, which anneals to complementary sequences on a DNA acceptor template to enable (+) strand transfer. We used model templates composed of primed (-) strand DNA covalently linked with post-transcriptionally modified tRNA(3)(lys) along with natural sequence human immunodeficiency virus (HIV) acceptor DNA to study the generation of the (+) strand strong stop intermediate and the subsequent (+) strand transfer reaction. The rate of formation of the (+) strand transfer reaction products was modestly increased (threefold) by inclusion of nucleocapsid protein, suggesting an ancillary role for this protein in this stage of retroviral replication. In addition to the well-known stop site opposite G59 of the tRNA primer, we detected two additional stop sites opposite psi55 and at A38. Kinetic analysis showed that only the intermediates formed by stops opposite G59 and psi55 were active in the subsequent (+) strand transfer reaction. The surprising discovery of the longer, viable (+) strand interaction intermediate prompted us to survey retroviral sequences for a region complementary to the additional donor DNA nucleotides involved in this over-extension. Indeed, complementary sequences that could support this over-extension were found. A strong consensus sequence is immediately adjacent to and downstream of the PBS in lentiviruses and spumaviruses. This consensus sequence was not found in other genera of retroviruses. We have named this element the "primer over-extension sequence" (POS), and propose that it provides a complementary sequence for strand transfer reactions proceeding from intermediates that extend beyond the standard 18 nt complement of the PBS.
机译:当前的逆转录病毒复制模型提出,在(+)链合成过程中,初始(-)链tRNA引物被部分复制以复制18 nt引物结合位点(PBS)。随后从(-)链模板中去除tRNA引物会使PBS暴露,该PBS与DNA受体模板上的互补序列退火以实现(+)链转移。我们使用由与转录后修饰的tRNA(3)(lys)共价连接的引发(-)链DNA以及自然序列人类免疫缺陷病毒(HIV)受体DNA组成的模型模板来研究(+)链强终止基因的产生中间和随后的(+)链转移反应。 (+)链转移反应产物的形成速率通过包含核衣壳蛋白而适度增加(三倍),表明该蛋白在逆转录病毒复制的这一阶段具有辅助作用。除了与tRNA引物G59相对的众所周知的终止位点外,我们还在psi55和A38处检测到两个额外的终止位点。动力学分析表明,仅由与G59和psi55对立的终止子形成的中间体在随后的(+)链转移反应中具有活性。更长,可行的(+)链相互作用中间体的惊人发现促使我们研究逆转录病毒序列,寻找与该过度延伸所涉及的其他供体DNA核苷酸互补的区域。确实,发现了可以支持这种过度延伸的互补序列。在慢病毒和弓形病毒中,强共有序列紧邻PBS并在PBS的下游。在其他逆转录病毒属中未发现该共有序列。我们将该元素命名为“引物过度延伸序列”(POS),并提出它为从超出PBS标准18 nt互补序列的中间体开始的链转移反应提供了一个互补序列。

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