McLennan Alexander G
School of Biological Sciences, University of Liverpool, Crown Street, Liverpool, L69 7ZB, UK.
Trends Biochem Sci. 2007 Jul;32(7):297-9. doi: 10.1016/j.tibs.2007.05.001. Epub 2007 May 10.
Cellular infection by vaccinia virus involves the controlled degradation of early, intermediate and late viral mRNAs, and increased turnover of host mRNAs. A new study has identified a key mediator of both these processes. A Nudix hydrolase encoded by the viral D10 gene decaps these mRNAs, thus targeting them for destruction independently of cellular systems. This finding has several implications for virus evolution and the regulation of RNA decapping.
痘苗病毒的细胞感染涉及早期、中期和晚期病毒mRNA的可控降解,以及宿主mRNA周转的增加。一项新研究已确定了这两个过程的关键介质。病毒D10基因编码的一种Nudix水解酶使这些mRNA脱帽,从而使其独立于细胞系统而被靶向破坏。这一发现对病毒进化和RNA脱帽调控有若干影响。