Wang Z, Kiledjian M
Department of Cell Biology and Neuroscience, Rutgers University, 604 Allison Road, Piscataway, NJ 08854, USA.
Cell. 2001 Dec 14;107(6):751-62. doi: 10.1016/s0092-8674(01)00592-x.
Mechanistic understanding of mammalian mRNA turnover remains incomplete. We demonstrate that the 3' to 5' exoribonuclease decay pathway is a major contributor to mRNA decay both in cells and in cell extract. An exoribonuclease-dependent scavenger decapping activity was identified that follows decay of the mRNA and hydrolyzes the residual cap. The decapping activity is associated with a subset of the exosome proteins in vivo, implying a higher-order degradation complex consisting of exoribonucleases and a decapping activity, which together coordinate the decay of an mRNA. These findings indicate that following deadenylation of mammal mRNA, degradation proceeds by a coupled 3' to 5' exoribonucleolytic activity and subsequent hydrolysis of the cap structure by a scavenger decapping activity.
对哺乳动物mRNA周转的机制理解仍不完整。我们证明,3'至5'外切核糖核酸酶降解途径是细胞和细胞提取物中mRNA降解的主要贡献者。我们鉴定出一种依赖外切核糖核酸酶的清除去帽活性,它在mRNA降解后起作用并水解残留的帽结构。在体内,这种去帽活性与外切体蛋白的一个亚群相关联,这意味着存在一个由外切核糖核酸酶和去帽活性组成的高阶降解复合体,它们共同协调mRNA的降解。这些发现表明,哺乳动物mRNA脱腺苷酸化后,降解通过3'至5'外切核糖核酸酶活性的偶联以及随后由清除去帽活性对帽结构的水解来进行。