Mechanism and regulation of the nonsense-mediated decay pathway

被引:332
|
作者
Hug, Nele [1 ]
Longman, Dasa [1 ]
Caceres, Javier F. [1 ]
机构
[1] Univ Edinburgh, Western Gen Hosp, Inst Genet & Mol Med, MRC,Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
MESSENGER-RNA DECAY; EXON-JUNCTION COMPLEX; UNFOLDED PROTEIN RESPONSE; NMD FACTORS; SURVEILLANCE MACHINERY; TERMINATION CODONS; QUALITY-CONTROL; AMPLIFIED GENE; CORE COMPLEX; UPF1; BINDING;
D O I
10.1093/nar/gkw010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Nonsense-mediated mRNA decay (NMD) pathway selectively degrades mRNAs harboring premature termination codons (PTCs) but also regulates the abundance of a large number of cellular RNAs. The central role of NMD in the control of gene expression requires the existence of buffering mechanisms that tightly regulate the magnitude of this pathway. Here, we will focus on the mechanism of NMD with an emphasis on the role of RNA helicases in the transition from NMD complexes that recognize a PTC to those that promote mRNA decay. We will also review recent strategies aimed at uncovering novel trans-acting factors and their functional role in the NMD pathway. Finally, we will describe recent progress in the study of the physiological role of the NMD response.
引用
收藏
页码:1483 / 1495
页数:13
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