Beerens N, Groot F, Berkhout B
Department of Human Retrovirology, Academic Medical Center, University of Amsterdam, 1100 DE Amsterdam, The Netherlands.
J Biol Chem. 2001 Aug 17;276(33):31247-56. doi: 10.1074/jbc.M102441200. Epub 2001 May 30.
Reverse transcription of the human immunodeficiency virus type 1 (HIV-1) RNA genome appears to be strictly regulated at the level of initiation. The primer binding site (PBS), at which the tRNA(3)(Lys) molecule anneals and reverse transcription is initiated, is present in a highly structured region of the untranslated leader RNA. Detailed mutational analysis of the U5 leader stem identified a sequence motif in the U5 region that is critical for activation of the PBS-bound tRNA(3)(Lys) primer. This U5 motif, termed the primer activation signal (PAS), may interact with the TPsiC arm of the tRNA(3)(Lys) primer, similar to the additional interaction proposed for the genome of Rous sarcoma virus and its tRNA(Trp) primer. This suggests that reverse transcription is regulated by a common mechanism in all retroviruses. In HIV-1, the PAS is masked through base pairing in the U5 leader stem. This provides a mechanism for positive and negative regulation of reverse transcription. Based on structure probing of the mutant and wild-type RNAs, an RNA secondary structure model is proposed that juxtaposes the critical PAS and PBS motifs.
人类免疫缺陷病毒1型(HIV-1)RNA基因组的逆转录似乎在起始水平受到严格调控。引物结合位点(PBS)是tRNA3(Lys)分子退火并启动逆转录的位点,它位于未翻译前导RNA的高度结构化区域。对U5前导茎的详细突变分析确定了U5区域中的一个序列基序,该基序对于激活与PBS结合的tRNA3(Lys)引物至关重要。这个U5基序被称为引物激活信号(PAS),它可能与tRNA3(Lys)引物的TPsiC臂相互作用,类似于对劳斯肉瘤病毒基因组及其tRNA(Trp)引物提出的额外相互作用。这表明逆转录在所有逆转录病毒中受一种共同机制调控。在HIV-1中,PAS通过U5前导茎中的碱基配对被掩盖。这为逆转录的正负调控提供了一种机制。基于对突变体和野生型RNA的结构探测,提出了一个RNA二级结构模型,该模型将关键的PAS和PBS基序并列在一起。