Lee M S, Craigie R
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9823-7. doi: 10.1073/pnas.91.21.9823.
An essential step in the retrovirus life cycle is integration of a DNA copy of the viral genome into a host chromosome. After reverse transcription, there can be a delay of many hours before the viral DNA is integrated. It is important for the retrovirus to ensure that the viral DNA does not integrate into itself during this period; such autointegration is a suicidal process that would result in destruction of the viral genome. Understanding of the mechanism that blocks autointegration of the viral DNA may lead to insights into how to inhibit viral replication by inducing the viral DNA to autointegrate. Evidence is presented in this report that viral nucleoprotein complexes isolated from cells infected with Moloney murine leukemia virus exhibit a barrier to autointegration. The barrier can be disrupted by high salt treatment and, subsequently, restored by addition of factors provided by a host cell extract. Our data indicate an involvement of host machinery in protecting retroviral DNA from autointegration.
逆转录病毒生命周期中的一个关键步骤是将病毒基因组的DNA拷贝整合到宿主染色体中。逆转录后,病毒DNA整合之前可能会有长达数小时的延迟。对于逆转录病毒来说,确保在此期间病毒DNA不会自身整合非常重要;这种自身整合是一个自杀过程,会导致病毒基因组的破坏。了解阻止病毒DNA自身整合的机制可能会为如何通过诱导病毒DNA自身整合来抑制病毒复制提供思路。本报告提供的证据表明,从感染莫洛尼氏鼠白血病病毒的细胞中分离出的病毒核蛋白复合物对自身整合具有屏障作用。该屏障可通过高盐处理破坏,随后通过添加宿主细胞提取物提供的因子得以恢复。我们的数据表明宿主机制参与保护逆转录病毒DNA免受自身整合。