Lemay Julie, Maidou-Peindara Priscilla, Cancio Reynel, Ennifar Eric, Coadou Gaël, Maga Giovanni, Rain Jean-Christophe, Benarous Richard, Liu Lang Xia
Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France.
J Mol Biol. 2008 Nov 21;383(4):783-96. doi: 10.1016/j.jmb.2008.08.055. Epub 2008 Aug 29.
Like all retroviruses, human immunodeficiency virus type 1 (HIV-1) undergoes reverse transcription during its replication cycle. The cellular cofactors potentially involved in this process still remain to be identified. We show here that A-kinase anchoring protein 149 (AKAP149) interacts with HIV-1 reverse transcriptase (RT) in both the yeast two-hybrid system and human cells. The AKAP149 binding site has been mapped to the RNase H domain of HIV-1 RT. AKAP149 silencing by RNA interference in HIV-1-infected cells inhibited viral replication at the reverse transcription step. We selected single-point mutants of RT defective for AKAP149 binding and demonstrated that mutant G462R, despite retaining significant intrinsic RT activity in vitro, failed to carry out HIV-1 reverse transcription correctly in infected cells. This suggests that the interaction between RT and AKAP149 in infected cells may play an important role in HIV-1 reverse transcription.
与所有逆转录病毒一样,1型人类免疫缺陷病毒(HIV-1)在其复制周期中会经历逆转录过程。可能参与这一过程的细胞辅助因子仍有待确定。我们在此表明,A激酶锚定蛋白149(AKAP149)在酵母双杂交系统和人类细胞中均与HIV-1逆转录酶(RT)相互作用。AKAP149的结合位点已定位到HIV-1 RT的核糖核酸酶H结构域。通过RNA干扰使HIV-1感染细胞中的AKAP149沉默,在逆转录步骤抑制了病毒复制。我们选择了对AKAP149结合有缺陷的RT单点突变体,并证明突变体G462R尽管在体外保留了显著的内在RT活性,但在感染细胞中无法正确进行HIV-1逆转录。这表明感染细胞中RT与AKAP149之间的相互作用可能在HIV-1逆转录中起重要作用。