Déctor Miguel Angel, Romero Pedro, López Susana, Arias Carlos F
Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Av. Universidad 2001, Cuernavaca, Morelos 62210, Mexico.
EMBO Rep. 2002 Dec;3(12):1175-80. doi: 10.1093/embo-reports/kvf234. Epub 2002 Nov 21.
RNA interference is an evolutionarily conserved double-stranded RNA-triggered mechanism for suppressing gene expression. Rotaviruses, the leading cause of severe diarrhea in young children, are formed by three concentric layers of protein, from which the spike protein VP4 projects. Here, we show that a small interfering RNA corresponding to the VP4 gene efficiently inhibits the synthesis of this protein in virus-infected cells. A large proportion of infected cells had no detectable VP4 and the yield of viral progeny was reduced. Most of the virus particles purified from these cells were triple-layered, but lacked VP4, and were poorly infectious. We also show that VP4 might not be required for the last step of virus morphogenesis. The VP4 gene silencing was specific, since the synthesis of VP4 from rotavirus strains that differ in the target sequence was not affected. These findings offer the possibility of carrying out reverse genetics in rotaviruses.
RNA干扰是一种由双链RNA触发的、在进化上保守的基因表达抑制机制。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组成,刺突蛋白VP4从其中伸出。在此,我们表明,与VP4基因对应的小干扰RNA能有效抑制病毒感染细胞中该蛋白的合成。很大一部分受感染细胞检测不到VP4,病毒子代产量降低。从这些细胞中纯化出的大多数病毒颗粒是三层的,但缺乏VP4,且感染性很差。我们还表明,病毒形态发生的最后一步可能不需要VP4。VP4基因沉默具有特异性,因为来自靶序列不同的轮状病毒株的VP4合成不受影响。这些发现为在轮状病毒中进行反向遗传学研究提供了可能性。