Identifying the right stop:: determining how the surveillance complex recognizes and degrades an aberrant mRNA

被引:120
作者
Ruiz-Echevarría, MJ
González, CI
Peltz, SW
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol Genet & Microbiol, Piscataway, NJ 08854 USA
[2] Canc Inst New Jersey, Piscataway, NJ 08854 USA
关键词
cis-acting stability elements; cis-acting instability elements; mRNA decay; nonsense mutations; translation termination;
D O I
10.1093/emboj/17.2.575
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 mRNA decay (NMD) pathway functions by checking whether translation termination has occurred prematurely and subsequently degrading the aberrant mRNAs, In Saccharomyces cerevisiae, it has been proposed that a surveillance complex scans 3' of the premature termination codon and searches for the downstream element (DSE), whose recognition by the complex identifies the transcript as aberrant and promotes its rapid decay, The results presented here suggest that translation termination is important for assembly of the surveillance complex, Neither the activity of the initiation ternary complex after premature translation termination has occurred nor the elongation phase of translation are essential for the activity of the NMD pathway, Once assembled, the surveillance complex is active for searching and recognizing a DSE for similar to 200 nt 3' of the stop codon, We have also identified a stabilizer sequence (STE) in the GCN4 leader region that inactivates the NMD pathway, Inactivation of the NMD pathway, as a consequence of either the DSE being too far from a stop codon or the presence of the STE, can be circumvented by inserting sequences containing a new translation initiation/termination cycle immediately 5' of the DSE, Further, the results indicate that the STE functions in the context of the GCN4 transcript to inactivate the NMD pathway.
引用
收藏
页码:575 / 589
页数:15
相关论文
共 58 条
[1]  
ABASTADO JP, 1991, NEW BIOL, V3, P511
[2]   SUPPRESSION OF RIBOSOMAL REINITIATION AT UPSTREAM OPEN READING FRAMES IN AMINO ACID-STARVED CELLS FORMS THE BASIS FOR GCN4 TRANSLATIONAL CONTROL [J].
ABASTADO, JP ;
MILLER, PF ;
JACKSON, BM ;
HINNEBUSCH, AG .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :486-496
[3]   SELECTIVE DESTABILIZATION OF SHORT-LIVED MESSENGER-RNAS WITH THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AU-RICH 3' NONCODING REGION IS MEDIATED BY A COTRANSLATIONAL MECHANISM [J].
AHARON, T ;
SCHNEIDER, RJ .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (03) :1971-1980
[4]   The catalytic subunit of protein phosphatase 2A associates with the translation termination factor eRF1 [J].
Andjelkovic, N ;
Zolnierowicz, S ;
VanHoof, C ;
Goris, J ;
Hemmings, BA .
EMBO JOURNAL, 1996, 15 (24) :7156-7167
[5]  
Ausubel F.M., 1992, CURRENT PROTOCOLS MO
[6]  
BEELMAN CA, 1994, J BIOL CHEM, V269, P9687
[7]  
Cao JH, 1996, MOL CELL BIOL, V16, P7109
[8]   Mechanisms and control of mRNA turnover in Saccharomyces cerevisiae [J].
Caponigro, G ;
Parker, R .
MICROBIOLOGICAL REVIEWS, 1996, 60 (01) :233-+
[9]  
Clemens MJ, 1996, TRANSLATIONAL CONTRO, P139
[10]   IDENTIFICATION AND CHARACTERIZATION OF GENES THAT ARE REQUIRED FOR THE ACCELERATED DEGRADATION OF MESSENGER-RNAS CONTAINING A PREMATURE TRANSLATIONAL TERMINATION CODON [J].
CUI, Y ;
HAGAN, KW ;
ZHANG, SA ;
PELTZ, SW .
GENES & DEVELOPMENT, 1995, 9 (04) :423-436