Girod A, Drynda A, Cosset F L, Verdier G, Ronfort C
Centre de Génétique Moléculaire et Cellulaire, Centre National de laRecherche Scientifique UMR 5534, Villeurbanne, France.
J Virol. 1996 Aug;70(8):5651-7. doi: 10.1128/JVI.70.8.5651-5657.1996.
We previously described avian leukosis virus-based packaging cell lines that produce stocks of retroviral vectors in which replication-competent viruses were not detectable. However, following infection of target cells with these retroviral stocks, we recently obtained colonies resulting from the transmission of recombinant genomes. Here, we have analyzed their genetic structure and shown that (i) each of them results from recombination between the packaging- and integration-defective transcomplementing genomes and the retroviral vector; (ii) recombination probably occurred during the reverse transcription step, involving strand switching of the reverse transcription growing point from the infectious retroviral vector to the transcomplementing RNA; and (iii) sequence identity and nonhomologous sequences were both used for the strand switching.
我们之前描述了基于禽白血病病毒的包装细胞系,这些细胞系可产生逆转录病毒载体储备液,在其中未检测到具有复制能力的病毒。然而,在用这些逆转录病毒储备液感染靶细胞后,我们最近获得了由重组基因组传递产生的菌落。在此,我们分析了它们的遗传结构,并表明:(i)它们中的每一个都是由包装缺陷和整合缺陷的反式互补基因组与逆转录病毒载体之间的重组产生的;(ii)重组可能发生在逆转录步骤中,涉及逆转录生长点从感染性逆转录病毒载体到反式互补RNA的链转移;(iii)序列同一性和非同源序列均用于链转移。