Michael N L, Morrow P, Mosca J, Vahey M, Burke D S, Redfield R R
Department of Retroviral Research, Walter Reed Army Institute of Research, Rockville, Maryland 20850.
J Virol. 1991 Mar;65(3):1291-303. doi: 10.1128/JVI.65.3.1291-1303.1991.
We have analyzed the kinetics of human immunodeficiency virus type 1 (HIV-1) RNA induction in chronically infected T cells and promonocytes. A substantial amount of spliced mRNAs and assembled virions was found in resting cells. Induction increased the steady-state level of total HIV-1 RNA by 4-fold but increased the level of unspliced transcripts by 25-fold. This increase in unspliced RNA was reflected in the amount of virus seen by electron microscopy. These data suggest a mechanism for the induction of HIV-1 RNA in chronically infected cells involving a shift in splicing greatly favoring the stability of unspliced viral RNA with only a modest increase in total viral RNA. Analysis of the relative abundance of transcript classes is critical to the measurement of HIV-1 viral replication kinetics.
我们分析了1型人类免疫缺陷病毒(HIV-1)RNA在慢性感染的T细胞和原单核细胞中的诱导动力学。在静息细胞中发现了大量剪接的mRNA和组装的病毒颗粒。诱导使HIV-1总RNA的稳态水平增加了4倍,但未剪接转录本的水平增加了25倍。未剪接RNA的这种增加反映在电子显微镜下观察到的病毒数量上。这些数据提示了一种慢性感染细胞中HIV-1 RNA诱导的机制,该机制涉及剪接的转变,极大地有利于未剪接病毒RNA的稳定性,而病毒总RNA仅适度增加。转录本类别相对丰度的分析对于测量HIV-1病毒复制动力学至关重要。