He Feng, Jacobson Allan
Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, Massachusetts 01655; email:
Annu Rev Genet. 2015;49:339-66. doi: 10.1146/annurev-genet-112414-054639. Epub 2015 Oct 2.
Nonsense-mediated mRNA decay (NMD) is a eukaryotic surveillance mechanism that monitors cytoplasmic mRNA translation and targets mRNAs undergoing premature translation termination for rapid degradation. From yeasts to humans, activation of NMD requires the function of the three conserved Upf factors: Upf1, Upf2, and Upf3. Here, we summarize the progress in our understanding of the molecular mechanisms of NMD in several model systems and discuss recent experiments that address the roles of Upf1, the principal regulator of NMD, in the initial targeting and final degradation of NMD-susceptible mRNAs. We propose a unified model for NMD in which the Upf factors provide several functions during premature termination, including the stimulation of release factor activity and the dissociation and recycling of ribosomal subunits. In this model, the ultimate degradation of the mRNA is the last step in a complex premature termination process.
无义介导的mRNA衰变(NMD)是一种真核生物监测机制,可监测细胞质mRNA的翻译,并将经历过早翻译终止的mRNA作为靶标进行快速降解。从酵母到人类,NMD的激活需要三种保守的Upf因子发挥作用:Upf1、Upf2和Upf3。在此,我们总结了在几个模型系统中对NMD分子机制的理解进展,并讨论了近期关于NMD主要调节因子Upf1在易受NMD影响的mRNA的初始靶向和最终降解中作用的实验。我们提出了一个NMD的统一模型,其中Upf因子在过早终止过程中发挥多种功能,包括刺激释放因子活性以及核糖体亚基的解离和再循环。在这个模型中,mRNA的最终降解是复杂的过早终止过程的最后一步。