Novina Carl D, Murray Michael F, Dykxhoorn Derek M, Beresford Paul J, Riess Jonathan, Lee Sang-Kyung, Collman Ronald G, Lieberman Judy, Shankar Premlata, Sharp Phillip A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Nat Med. 2002 Jul;8(7):681-6. doi: 10.1038/nm725. Epub 2002 Jun 3.
RNA interference silences gene expression through short interfering 21 23-mer double-strand RNA segments that guide mRNA degradation in a sequence-specific fashion. Here we report that siRNAs inhibit virus production by targeting the mRNAs for either the HIV-1 cellular receptor CD4, the viral structural Gag protein or green fluorescence protein substituted for the Nef regulatory protein. siRNAs effectively inhibit pre- and/or post-integration infection events in the HIV-1 life cycle. Thus, siRNAs may have potential for therapeutic intervention in HIV-1 and other viral infections.
RNA干扰通过短干扰性21 - 23聚体双链RNA片段使基因表达沉默,这些片段以序列特异性方式引导mRNA降解。在此我们报告,小干扰RNA(siRNAs)通过靶向HIV-1细胞受体CD4、病毒结构蛋白Gag或替代Nef调节蛋白的绿色荧光蛋白的mRNA来抑制病毒产生。siRNAs有效抑制HIV-1生命周期中的整合前和/或整合后感染事件。因此,siRNAs可能在HIV-1和其他病毒感染的治疗干预方面具有潜力。