Overexpression of truncated Nmd3p inhibits protein synthesis in yeast

被引:28
作者
Belk, JP [1 ]
He, F [1 ]
Jacobson, A [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01655 USA
关键词
mRNA; nonsense-mediated mRNA decay; ribosome; rRNA processing;
D O I
10.1017/S1355838299990027
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 yeast NMD3 gene was identified in a two-hybrid screen using the nonsense-mediated mRNA decay factor, Upf1p, as bait. NMD3 was shown to encode an essential, highly conserved protein that associated principally with free 60S ribosomal subunits. Overexpression of a truncated form of Nmd3p, lacking 100 C-terminal amino acids and most of its Upf1p-interacting domain, had dominant-negative effects on both cell growth and protein synthesis and promoted the formation of polyribosome half-mers. These effects were eliminated by truncation of an additional 100 amino acids from Nmd3p. Overexpression of the nmd3 Delta 100 allele also led to increased synthesis and destabilization of some ribosomal protein mRNAs, and increased synthesis and altered processing of 35S pre-rRNA. Our data suggest that Nmd3p has a role in the formation, function, or maintenance of the 60S ribosomal subunit and may provide a link for Upf1p to 80S monosomes.
引用
收藏
页码:1055 / 1070
页数:16
相关论文
共 61 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Relationship between yeast polyribosomes and Upf proteins required for nonsense mRNA decay [J].
Atkin, AL ;
Schenkman, LR ;
Eastham, M ;
Dahlseid, JN ;
Lelivelt, MJ ;
Culbertson, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (35) :22163-22172
[3]  
ATKIN AL, 1995, MOL BIOL CELL, V6, P611
[4]   An essential component of the decapping enzyme required for normal rates of mRNA turnover [J].
Beelman, CA ;
Stevens, A ;
Caponigro, G ;
LaGrandeur, TE ;
Hatfield, L ;
Fortner, DM ;
Parker, R .
NATURE, 1996, 382 (6592) :642-646
[5]  
BOORSTEIN WR, 1989, METHOD ENZYMOL, V180, P347
[6]   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
[7]  
CZAPLINSKI K, 1995, RNA, V1, P610
[8]   The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs [J].
Czaplinski, K ;
Ruiz-Echevarria, MJ ;
Paushkin, SV ;
Han, X ;
Weng, YM ;
Perlick, HA ;
Dietz, HC ;
Ter-Avanesyan, MD ;
Peltz, SW .
GENES & DEVELOPMENT, 1998, 12 (11) :1665-1677
[9]   MECHANISMS OF MESSENGER-RNA DEGRADATION IN EUKARYOTES [J].
DECKER, CJ ;
PARKER, R .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (08) :336-340
[10]   A TURNOVER PATHWAY FOR BOTH STABLE AND UNSTABLE MESSENGER-RNAS IN YEAST - EVIDENCE FOR A REQUIREMENT FOR DEADENYLATION [J].
DECKER, CJ ;
PARKER, R .
GENES & DEVELOPMENT, 1993, 7 (08) :1632-1643