Trans-translation:: The tmRNA-mediated surveillance mechanism for ribosome rescue, directed protein degradation, and nonstop mRNA decay

被引:70
作者
Dulebohn, Daniel
Choy, Jennifer
Sundermeier, Thomas
Okan, Nihal
Karzai, A. Wali [1 ]
机构
[1] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Ctr Infect Dis, Stony Brook, NY 11794 USA
关键词
D O I
10.1021/bi6026055
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 accurate flow of genetic information from DNA to RNA to protein is essential for all living organisms. An astonishing array of quality-assurance mechanisms have evolved to ensure that high degree of fidelity is maintained at every stage of this process. One of the most fascinating quality-control mechanisms involves tmRNA, also known as SsrA or 10Sa RNA. tmRNA is a versatile and highly conserved bacterial molecule endowed with the combined structural and functional properties of both a tRNA and a mRNA. The tmRNA system orchestrates three key biological functions: (1) recognition and rescue of ribosomes stalled on aberrant mRNAs, (2) disposal of the causative defective mRNAs, and (3) addition of a degradation tag to ribosome-associated protein fragments for directed proteolysis. Although not essential in Escherichia coli, tmRNA activity is essential for bacterial survival under adverse conditions and for virulence in some, and perhaps all, pathogenic bacteria. Recent evidence suggests that in addition to its quality-control function the tmRNA system might also play a key regulatory role in certain physiological pathways. This review will focus on recent advances in our understanding of the structural properties, mechanistic details, and physiological significance of this unique RNA and its principal protein partners.
引用
收藏
页码:4681 / 4693
页数:13
相关论文
共 102 条
[1]   SsrA-mediated tagging and proteolysis of Lacl and its role in the regulation of lac operon [J].
Abo, T ;
Inada, T ;
Ogawa, A ;
Aiba, H .
EMBO JOURNAL, 2000, 19 (14) :3762-3769
[2]   3-DIMENSIONAL STRUCTURE OF THE RIBOSOMAL TRANSLOCASE - ELONGATION-FACTOR-G FROM THERMUS-THERMOPHILUS [J].
AEVARSSON, A ;
BRAZHNIKOV, E ;
GARBER, M ;
ZHELTONOSOVA, J ;
CHIRGADZE, Y ;
AL-KARADAGHI, S ;
SVENSSON, LA ;
LILJAS, A .
EMBO JOURNAL, 1994, 13 (16) :3669-3677
[3]   10Sa RNA complements the temperature-sensitive phenotype caused by a mutation in the phosphoribosyl pyrophosphate synthetase (prs) gene in Escherichia coli [J].
Ando, H ;
Kitabatake, M ;
Inokuchi, H .
GENES & GENETIC SYSTEMS, 1996, 71 (01) :47-50
[4]   ATP-dependent proteases of bacteria: recognition logic and operating principles [J].
Baker, Tania A. ;
Sauer, Robert T. .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (12) :647-653
[5]   Kinetic parameters for tmRNA binding to alanyl-tRNA synthetase and elongation factor Tu from Escherichia coli [J].
Barends, S ;
Wower, J ;
Kraal, B .
BIOCHEMISTRY, 2000, 39 (10) :2652-2658
[6]   Functional evidence for D- and T-loop interactions in tmRNA [J].
Barends, S ;
Björk, K ;
Gultyaev, AP ;
de Smit, MH ;
Pleij, CWA ;
Kraal, B .
FEBS LETTERS, 2002, 514 (01) :78-83
[7]   Simultaneous and functional binding of SmpB and EF-Tu • GTP to the alanyl acceptor arm of tmRNA [J].
Barends, S ;
Karzai, AW ;
Sauer, RT ;
Wower, J ;
Kraal, B .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 314 (01) :9-21
[8]  
BAUMLER AJ, 1994, INFECT IMMUN, V62, P1623
[9]   X-ray crystal structures of 70S ribosome functional complexes [J].
Cate, JH ;
Yusupov, MM ;
Yusupova, GZ ;
Earnest, TN ;
Noller, HF .
SCIENCE, 1999, 285 (5436) :2095-2104
[10]   Strong selective pressure to use G:U to mark an RNA acceptor stem for alanine [J].
Chihade, JW ;
Hayashibara, K ;
Shiba, K ;
Schimmel, P .
BIOCHEMISTRY, 1998, 37 (25) :9193-9202