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Nonsense-mediated mRNA decay in human cells: mechanistic insights, functions beyond quality control and the double-life of NMD factors
被引:265
作者:
Nicholson, Pamela
[1
]
Yepiskoposyan, Hasmik
[1
]
Metze, Stefanie
[1
]
Orozco, Rodolfo Zamudio
[1
]
Kleinschmidt, Nicole
[1
]
Muehlemann, Oliver
[1
]
机构:
[1] Univ Bern, Inst Cell Biol, CH-3012 Bern, Switzerland
基金:
瑞士国家科学基金会;
欧洲研究理事会;
关键词:
NMD;
Nonsense mRNA surveillance;
Post-transcriptional gene regulation;
PTC;
mRNA turnover;
EXON-JUNCTION COMPLEX;
IMMUNODEFICIENCY-VIRUS TYPE-1;
INSERTION-SEQUENCE-BINDING;
HISTONE GENE-EXPRESSION;
REPEAT-CONTAINING RNA;
BETA-GLOBIN GENE;
P-BODY FORMATION;
SACCHAROMYCES-CEREVISIAE;
TRANSLATION TERMINATION;
CAENORHABDITIS-ELEGANS;
D O I:
10.1007/s00018-009-0177-1
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:
Nonsense-mediated decay is well known by the lucid definition of being a RNA surveillance mechanism that ensures the speedy degradation of mRNAs containing premature translation termination codons. However, as we review here, NMD is far from being a simple quality control mechanism; it also regulates the stability of many wild-type transcripts. We summarise the abundance of research that has characterised each of the NMD factors and present a unified model for the recognition of NMD substrates. The contentious issue of how and where NMD occurs is also discussed, particularly with regard to P-bodies and SMG6-driven endonucleolytic degradation. In recent years, the discovery of additional functions played by several of the NMD factors has further complicated the picture. Therefore, we also review the reported roles of UPF1, SMG1 and SMG6 in other cellular processes.
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页码:677 / 700
页数:24
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