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逆转录病毒包装细胞系的重新设计,以避免重组导致辅助病毒产生。

Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production.

作者信息

Miller A D, Buttimore C

出版信息

Mol Cell Biol. 1986 Aug;6(8):2895-902. doi: 10.1128/mcb.6.8.2895-2902.1986.

Abstract

Retrovirus vectors can be made in the absence of helper virus by using retrovirus packaging cell lines. Helper-free virus is critical for a variety of gene transfer studies. The most useful packaging cell lines contain helper virus DNA from which the signal required for packaging of the viral RNA genome into virions has been deleted. However, we showed that the ability to package virus is conferred at very low frequency to cells infected with virus from these packaging cell lines, presumably by low-frequency transmission of the deleted virus genome. In addition, these packaging cell lines can interact with some retroviral vectors to yield replication-competent virus. We constructed packaging cell lines containing helper virus DNA that had several alterations in addition to deletion of the packaging signal. The new packaging cells retained the useful features of previously available lines but did not yield helper virus after introduction of any of the vectors tested, and transfer of the packaging function was not detected.

摘要

通过使用逆转录病毒包装细胞系,可以在没有辅助病毒的情况下制备逆转录病毒载体。无辅助病毒对于各种基因转移研究至关重要。最有用的包装细胞系包含辅助病毒DNA,其中将病毒RNA基因组包装到病毒颗粒中所需的信号已被删除。然而,我们发现,从这些包装细胞系感染病毒的细胞以极低频率获得包装病毒的能力,推测是由于缺失的病毒基因组发生了低频传递。此外,这些包装细胞系可与某些逆转录病毒载体相互作用,产生具有复制能力的病毒。我们构建了包含辅助病毒DNA的包装细胞系,除了删除包装信号外,该DNA还有几处改变。新的包装细胞保留了先前可用细胞系的有用特性,但在引入任何测试载体后都不会产生辅助病毒,并且未检测到包装功能的转移。

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