Sun Lingling, Mailliot Justine, Schaffitzel Christiane
School of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, UK.
Bristol Engineering Biology Centre BrisEngBio, 24 Tyndall Ave, Bristol BS8 1TQ, UK.
Biomedicines. 2023 Feb 27;11(3):722. doi: 10.3390/biomedicines11030722.
Nonsense-mediated mRNA decay (NMD) is a cellular surveillance mechanism that degrades mRNAs with a premature stop codon, avoiding the synthesis of C-terminally truncated proteins. In addition to faulty mRNAs, NMD recognises ~10% of endogenous transcripts in human cells and downregulates their expression. The up-frameshift proteins are core NMD factors and are conserved from yeast to human in structure and function. In mammals, NMD diversified into different pathways that target different mRNAs employing additional NMD factors. Here, we review our current understanding of molecular mechanisms and cellular roles of NMD pathways and the involvement of more specialised NMD factors. We describe the consequences of mutations in NMD factors leading to neurodevelopmental diseases, and the role of NMD in cancer. We highlight strategies of RNA viruses to evade recognition and decay by the NMD machinery.
无义介导的mRNA降解(NMD)是一种细胞监测机制,可降解带有提前终止密码子的mRNA,避免合成C端截短的蛋白质。除了有缺陷的mRNA外,NMD还能识别约10%的人类细胞内源性转录本并下调其表达。移码上调蛋白是核心NMD因子,在结构和功能上从酵母到人类都具有保守性。在哺乳动物中,NMD分化为不同的途径,利用额外的NMD因子靶向不同的mRNA。在这里,我们综述了目前对NMD途径的分子机制和细胞作用以及更特殊的NMD因子的参与的理解。我们描述了NMD因子突变导致神经发育疾病的后果,以及NMD在癌症中的作用。我们强调了RNA病毒逃避NMD机制识别和降解的策略。