Arias Carlos F, Dector Miguel A, Segovia Lorenzo, López Tomás, Camacho Minerva, Isa Pavel, Espinosa Rafaela, López Susana
Departamento de Génetica del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Avenida Universidad 2001, Col. Chamilpa, Cuernavaca, Morelos 62210, Mexico.
Virus Res. 2004 Jun 1;102(1):43-51. doi: 10.1016/j.virusres.2004.01.014.
RNA interference (RNAi) is a double-stranded RNA (dsRNA)-triggered mechanism for suppressing gene expression, which is conserved in evolution and has emerged as a powerful tool to study gene function. Rotaviruses, the leading cause of severe diarrhea in young children, are formed by three concentric layers of protein, and a genome composed of 11 segments of dsRNA. Here, we show that the RNAi machinery can be triggered to silence rotavirus gene expression by sequence-specific short interfering RNAs (siRNAs). RNAi is also useful for the study of the virus-cell interactions, through the silencing of cellular genes that are potentially important for the replication of the virus. Interestingly, while the translation of mRNAs is readily stopped by the RNAi machinery, the viral transcripts involved in virus genome replication do not seem to be susceptible to RNAi. Since gene silencing by RNAi is very efficient and specific, this system could become a novel therapeutic approach for rotavirus and other virus infections, once efficient methods for in vivo delivery of siRNAs are developed. Although the use of RNAi as an antiviral therapeutic tool remains to be demonstrated, there is no doubt that this technology will influence drastically the way postgenomic virus research is conducted.
RNA干扰(RNAi)是一种由双链RNA(dsRNA)触发的抑制基因表达的机制,在进化过程中保守,已成为研究基因功能的强大工具。轮状病毒是幼儿严重腹泻的主要病因,由三层同心蛋白质层和由11段dsRNA组成的基因组构成。在此,我们表明RNAi机制可被序列特异性短干扰RNA(siRNA)触发,从而沉默轮状病毒基因表达。RNAi通过沉默对病毒复制可能重要的细胞基因,对研究病毒-细胞相互作用也很有用。有趣的是,虽然RNAi机制能轻易阻止mRNA的翻译,但参与病毒基因组复制的病毒转录本似乎对RNAi不敏感。由于RNAi介导的基因沉默非常高效且特异,一旦开发出有效的体内递送siRNA的方法,该系统可能成为治疗轮状病毒和其他病毒感染的新方法。尽管将RNAi用作抗病毒治疗工具仍有待证明,但毫无疑问,这项技术将极大地影响后基因组时代病毒研究的开展方式。