Regulation of nonsense-mediated mRNA decay

被引:99
作者
Huang, Lulu [1 ]
Wilkinson, Miles F. [1 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Reprod Med, La Jolla, CA 92093 USA
关键词
EXON-JUNCTION COMPLEX; CAENORHABDITIS-ELEGANS; HUMAN SMG-1; EMBRYONIC-DEVELOPMENT; SURVEILLANCE COMPLEX; CRYSTAL-STRUCTURE; MIRNA EXPRESSION; GENE-EXPRESSION; DIVERSE CLASSES; PROTEIN-KINASE;
D O I
10.1002/wrna.1137
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nonsense-mediated mRNA decay (NMD) is a highly conserved pathway that was originally identified as a RNA surveillance mechanism that degrades aberrant mRNAs harboring premature termination (nonsense) codons. Recently, it was discovered that NMD also regulates normal gene expression. Genome-wide studies showed that ablation of NMD alters the expression of similar to 10% of transcripts in a wide variety of eukaryotes. In general, NMD specifically targets normal transcripts that harbor a stop codon in a premature context. The finding that NMD regulates normal gene expression raises the possibility that NMD itself is subject to regulation. Indeed, recent studies have shown that NMD efficiency varies in different cell types and tissues. NMD is also subject to developmental control in both higher and lower eukaryotic species. Molecular mechanisms have been definedincluding those involving microRNAs and other RNA decay pathwaysthat regulate the magnitude of NMD in some developmental settings. This developmental regulation of NMD appears to have physiological roles, at least in some model systems. In addition to mechanisms that modulate the efficiency of NMD, mechanisms have recently been identified that serve the opposite purpose: to maintain the efficiency of NMD in the face of insults. This buffering is achieved by feedback networks that serve to regulate the stability of NMD factors. The discovery of NMD homeostasis and NMD regulatory mechanisms has important implications for how NMD acts in biological processes and how its magnitude could potentially be manipulated for clinical benefit. WIREs RNA 2012. doi: 10.1002/wrna.1137 For further resources related to this article, please visit the WIREs website.
引用
收藏
页码:807 / 828
页数:22
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