The enzymes and control of eukaryotic mRNA turnover

被引:648
作者
Parker, R
Song, HW
机构
[1] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
[2] Univ Arizona, Howard Hughes Med Inst, Tucson, AZ 85721 USA
[3] Inst Mol & Cell Biol, Lab Macromol Struct, Singapore 117609, Singapore
[4] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
关键词
D O I
10.1038/nsmb724
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 degradation of eukaryotic mRNAs plays important roles in the modulation of gene expression, quality control of mRNA biogenesis and antiviral defenses. In the past five years, many of the enzymes involved in this process have been identified and mechanisms that modulate their activities have begun to be identified. In this review, we describe the enzymes of mRNA degradation and their properties. We highlight that there are a variety of enzymes with different specificities, suggesting that individual nucleases act on distinct subpopulations of transcripts within the cell. In several cases, translation factors that bind mRNA inhibit these nucleases. In addition, recent work has begun to identify distinct mRNP complexes that recruit the nucleases to transcripts through different mRNA-interacting proteins. These properties and complexes suggest multiple mechanisms by which mRNA degradation could be regulated.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 106 条
[31]   Killing the messenger: Short RNAs that silence gene expression [J].
Dykxhoorn, DM ;
Novina, CD ;
Sharp, PA .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (06) :457-467
[32]   The DEAD box protein Dhh1 stimulates the decapping enzyme Dcp1 [J].
Fischer, N ;
Weis, K .
EMBO JOURNAL, 2002, 21 (11) :2788-2797
[33]   ELAV proteins stabilize deadenylated intermediates in a novel in vitro mRNA deadenylation/degradation system [J].
Ford, LP ;
Watson, J ;
Keene, JD ;
Wilusz, J .
GENES & DEVELOPMENT, 1999, 13 (02) :188-201
[34]   An mRNA surveillance mechanism that eliminates transcripts lacking termination codons [J].
Frischmeyer, PA ;
van Hoof, A ;
O'Donnell, K ;
Guerrerio, AL ;
Parker, R ;
Dietz, HC .
SCIENCE, 2002, 295 (5563) :2258-2261
[35]  
Fromont-Racine M, 2000, YEAST, V17, P95, DOI 10.1002/1097-0061(20000630)17:2<95::AID-YEA16>3.0.CO
[36]  
2-H
[37]   Interaction between a poly(A)-specific ribonuclease and the 5′ cap influences mRNA deadenylation rates in vitro [J].
Gao, M ;
Fritz, DT ;
Ford, LP ;
Wilusz, J .
MOLECULAR CELL, 2000, 5 (03) :479-488
[38]   Functional organization of the yeast proteome by systematic analysis of protein complexes [J].
Gavin, AC ;
Bösche, M ;
Krause, R ;
Grandi, P ;
Marzioch, M ;
Bauer, A ;
Schultz, J ;
Rick, JM ;
Michon, AM ;
Cruciat, CM ;
Remor, M ;
Höfert, C ;
Schelder, M ;
Brajenovic, M ;
Ruffner, H ;
Merino, A ;
Klein, K ;
Hudak, M ;
Dickson, D ;
Rudi, T ;
Gnau, V ;
Bauch, A ;
Bastuck, S ;
Huhse, B ;
Leutwein, C ;
Heurtier, MA ;
Copley, RR ;
Edelmann, A ;
Querfurth, E ;
Rybin, V ;
Drewes, G ;
Raida, M ;
Bouwmeester, T ;
Bork, P ;
Seraphin, B ;
Kuster, B ;
Neubauer, G ;
Superti-Furga, G .
NATURE, 2002, 415 (6868) :141-147
[39]   Posttranscriptional regulation of the RAD5 DNA repair gene by the Dun1 kinase and the Pan2-Pan3 poly(A)-nuclease complex contributes to survival of replication blocks [J].
Hammet, A ;
Pike, BL ;
Heierhorst, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) :22469-22474
[40]   IDENTIFICATION OF A NOVEL COMPONENT OF THE NONSENSE-MEDIATED MESSENGER-RNA DECAY PATHWAY BY USE OF AN INTERACTING PROTEIN SCREEN [J].
HE, F ;
JACOBSON, A .
GENES & DEVELOPMENT, 1995, 9 (04) :437-454