Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease

被引:330
作者
Khajavi, Mehrdad
Inoue, Ken
Lupski, James R.
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Natl Ctr Neurol Psychiat, Natl Inst Neurosci, Dept Mental Retardat & Birth Defect Res, Tokyo, Japan
[3] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Houston, TX 77030 USA
关键词
premature termination codons; nonsense-mediated decay; genotype-phenotype correlations;
D O I
10.1038/sj.ejhg.5201649
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 decay (NMD) pathway is an mRNA surveillance system that typically degrades transcripts containing premature termination codons (PTCs) in order to prevent translation of unnecessary or aberrant transcripts. Failure to eliminate these mRNAs with PTCs may result in the synthesis of abnormal proteins that can be toxic to cells through dominant-negative or gain-of-function effects. Recent studies have expanded our understanding of the mechanism by which nonsense transcripts are recognized and targeted for decay. Here, we review the physiological role of this surveillance pathway, its implications for human diseases, and why knowledge of NMD is important to an understanding of genotype-phenotype correlations in various genetic disorders.
引用
收藏
页码:1074 / 1081
页数:8
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