Park Wee-Sung, Miyano-Kurosaki Naoko, Hayafune Masaaki, Nakajima Emiko, Matsuzaki Tetsuo, Shimada Fumiyuki, Takaku Hiroshi
Department of Industrial Chemistry, Faculty of Engineering, Chiba Institute of Technology, 2-17-1 Tsudanuma, Narashino-shi, Chiba 275-0016, Japan.
Nucleic Acids Res. 2002 Nov 15;30(22):4830-5. doi: 10.1093/nar/gkf627.
The RNA interference (RNAi) phenomenon is a recently observed process in which the introduction of a double-stranded RNA (dsRNA) into a cell causes the specific degradation of a mRNA containing the same sequence. The 21-23 nt guide RNAs, generated by RNase III cleavage from longer dsRNAs, are associated with sequence-specific mRNA degradation. Here, we show that dsRNA specifically suppresses the expression of HIV-1 genes. To study dsRNA-mediated gene interference in HIV-1-infected cells, we have designed six long dsRNAs containing the HIV-1 gag and env genes. HIV-1 replication was totally suppressed in a sequence-specific manner by the dsRNAs in HIV-1-infected cells. Especially, E2 dsRNA containing the major CD4-binding domain sequence of gp120, as the target of the HIV-1 env gene, dramatically inhibited the expression of the HIV-1 p24 antigen in PBMCs for a relatively long time. The dsRNA interference method seems to be a promising new strategy for anti-HIV-1 gene therapeutics.
RNA干扰(RNAi)现象是最近观察到的一种过程,即向细胞中引入双链RNA(dsRNA)会导致含有相同序列的mRNA发生特异性降解。由较长dsRNA经核糖核酸酶III切割产生的21 - 23个核苷酸的引导RNA与序列特异性mRNA降解相关。在此,我们表明dsRNA可特异性抑制HIV - 1基因的表达。为了研究dsRNA介导的HIV - 1感染细胞中的基因干扰,我们设计了六种包含HIV - 1 gag和env基因的长dsRNA。在HIV - 1感染的细胞中,dsRNA以序列特异性方式完全抑制了HIV - 1的复制。特别是,作为HIV - 1 env基因靶点、包含gp120主要CD4结合域序列的E2 dsRNA,在相对较长时间内显著抑制了PBMC中HIV - 1 p24抗原的表达。dsRNA干扰方法似乎是一种有前景的抗HIV - 1基因治疗新策略。