Savatier P, Bagnis C, Thoraval P, Poncet D, Belakebi M, Mallet F, Legras C, Cosset F L, Thomas J L, Chebloune Y
Laboratoire de Biologie Cellulaire, INRA, CNRS UA92, Université Claude Bernard Lyon I, Villeurbanne, France.
J Virol. 1989 Feb;63(2):513-22. doi: 10.1128/JVI.63.2.513-522.1989.
We constructed an avian leukosis virus-based packaging cell line, pHF-g, containing Rous-associated virus DNA with several alterations to abolish RNA packaging. One of them is a 52-base-pair deletion encompassing the putative encapsidation signal in the leader region. The 3' long terminal repeat was also removed and replaced by the polyadenylation sequence from the herpes simplex virus thymidine kinase gene. When pHF-g cells were transfected by an avian leukosis virus-based vector, they produced replication-defective virus at high titer but they did not release any replication-competent particles. Proviral DNA was shown to be correctly integrated as well as correctly expressed. Viral RNAs were shown to be correctly translated into gag-related polypeptides.
我们构建了一种基于禽白血病病毒的包装细胞系pHF-g,其包含劳斯相关病毒DNA,并进行了若干改变以消除RNA包装。其中之一是在先导区缺失一个52个碱基对的片段,该片段包含假定的包装信号。3'长末端重复序列也被去除,并用单纯疱疹病毒胸苷激酶基因的聚腺苷酸化序列取代。当用基于禽白血病病毒的载体转染pHF-g细胞时,它们能高滴度产生复制缺陷型病毒,但不释放任何具有复制能力的颗粒。前病毒DNA被证明能正确整合并正确表达。病毒RNA被证明能正确翻译成与gag相关的多肽。