Kaminska Monika, Shalak Vyacheslav, Francin Mathilde, Mirande Marc
Laboratoire d'Enzymologie et Biochimie Structurales, CNRS, 1 Avenue de la Terrasse, 91190 Gif-sur-Yvette, France.
J Virol. 2007 Jan;81(1):68-73. doi: 10.1128/JVI.01267-06. Epub 2006 Oct 18.
The primer for reverse transcription of the human immunodeficiency virus type 1 (HIV-1) genome is tRNA3(Lys). During assembly of HIV-1 particles, tRNA3(Lys) is taken up from the host cell along with lysyl-tRNA synthetase (LysRS), the tRNA binding protein that specifically aminoacylates the different tRNA(Lys) isoacceptors. In humans, the cytoplasmic and mitochondrial species of LysRS are encoded by a single gene by means of alternative splicing. Here, we show that polyclonal antibodies directed to the full-length cytoplasmic enzyme equally recognized the two enzyme species. We raised antibodies against synthetic peptides that allowed discrimination between the two enzymes and found that mitochondrial LysRS is the only cellular source of LysRS detected in the virions. These results open new routes for understanding the molecular mechanisms involved in the specific packaging of tRNA3(Lys) into viral particles.
人类免疫缺陷病毒1型(HIV-1)基因组逆转录的引物是tRNA3(Lys)。在HIV-1病毒颗粒组装过程中,tRNA3(Lys)与赖氨酰-tRNA合成酶(LysRS)一起从宿主细胞中摄取,LysRS是一种tRNA结合蛋白,可特异性地将不同的tRNA(Lys)同工受体氨酰化。在人类中,LysRS的细胞质和线粒体形式由单个基因通过可变剪接编码。在这里,我们表明针对全长细胞质酶的多克隆抗体同样识别这两种酶形式。我们制备了针对合成肽的抗体,从而能够区分这两种酶,并发现线粒体LysRS是在病毒颗粒中检测到的LysRS的唯一细胞来源。这些结果为理解tRNA3(Lys)特异性包装到病毒颗粒中的分子机制开辟了新途径。