Muthuswami Rohini, Chen Joe, Burnett Bruce P, Thimmig Roberta L, Janjic Nebojsa, McHenry Charles S
Department of Biochemistry & Molecular Genetics and Molecular Biology Program, University of Colorado Health Sciences Center, 4200 E. Ninth Avenue, B121, Denver, CO 80262, USA.
J Mol Biol. 2002 Jan 18;315(3):311-23. doi: 10.1006/jmbi.2001.5205.
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.
当前的逆转录病毒复制模型提出,在(+)链合成过程中,最初的(-)链tRNA引物会被部分复制以重现18个核苷酸的引物结合位点(PBS)。随后从(-)链模板上移除tRNA引物会暴露出PBS,其与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tRNA3(lys)共价连接的引发(-)链DNA组成的模型模板,以及天然序列的人类免疫缺陷病毒(HIV)受体DNA,来研究(+)链强终止中间体的产生以及随后的(+)链转移反应。通过加入核衣壳蛋白,(+)链转移反应产物的形成速率适度增加(三倍),表明该蛋白在逆转录病毒复制的这一阶段起辅助作用。除了与tRNA引物的G59相对的众所周知的终止位点外,我们还检测到与psi55相对和在A38处的另外两个终止位点。动力学分析表明,只有由与G59和psi55相对的终止形成的中间体在随后的(+)链转移反应中具有活性。更长的、可行的(+)链相互作用中间体这一惊人发现促使我们在逆转录病毒序列中寻找与参与这种过度延伸的额外供体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。在慢病毒和泡沫病毒中,一个强共有序列紧邻PBS并在其下游。在其他逆转录病毒属中未发现该共有序列。我们将这个元件命名为“引物过度延伸序列”(POS),并提出它为从延伸超过PBS标准18个核苷酸互补序列的中间体进行的链转移反应提供互补序列。