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
[31]   Zinc fingers are sticking together [J].
Mackay, JP ;
Crossley, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (01) :1-4
[32]   A new nomenclature for the cytoplasmic ribosomal proteins Saccharomyces cerevisiae [J].
Mager, WH ;
Planta, RJ ;
Ballesta, JPG ;
Lee, JC ;
Mizuta, K ;
Suzuki, K ;
Warner, JR ;
Woolford, J .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4872-4875
[33]   Linking mRNA turnover and translation: Assessing the polyribosomal association of mRNA decay factors and degradative intermediates [J].
Mangus, DA ;
Jacobson, A .
METHODS, 1999, 17 (01) :28-37
[34]   The C-terminal silencing domain of Rap1p is essential for the repression of ribosomal protein genes in response to a defect in the secretory pathway [J].
Mizuta, K ;
Tsujii, R ;
Warner, JR ;
Nishiyama, M .
NUCLEIC ACIDS RESEARCH, 1998, 26 (04) :1063-1069
[35]   ASSOCIATION OF RAP1 BINDING-SITES WITH STRINGENT CONTROL OF RIBOSOMAL-PROTEIN GENE-TRANSCRIPTION IN SACCHAROMYCES-CEREVISIAE [J].
MOEHLE, CM ;
HINNEBUSCH, AG .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (05) :2723-2735
[36]   ASSEMBLY OF 60S RIBOSOMAL-SUBUNITS IS PERTURBED IN TEMPERATURE-SENSITIVE YEAST MUTANTS DEFECTIVE IN RIBOSOMAL-PROTEIN L16 [J].
MORITZ, M ;
PULASKI, BA ;
WOOLFORD, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (11) :5681-5692
[37]   DEADENYLATION OF THE UNSTABLE MESSENGER-RNA ENCODED BY THE YEAST MFA2 GENE LEADS TO DECAPPING FOLLOWED BY 5'-]3' DIGESTION OF THE TRANSCRIPT [J].
MUHLRAD, D ;
DECKER, CJ ;
PARKER, R .
GENES & DEVELOPMENT, 1994, 8 (07) :855-866
[38]  
MUHLRAD D, 1995, MOL CELL BIOL, V15, P2145
[39]   PREMATURE TRANSLATIONAL TERMINATION TRIGGERS MESSENGER-RNA DECAPPING [J].
MUHLRAD, D ;
PARKER, R .
NATURE, 1994, 370 (6490) :578-581
[40]   EFFECTS OF PROGRESSIVE DEPLETION OF TCM1 OR CYH2 MESSENGER-RNA ON SACCHAROMYCES-CEREVISIAE RIBOSOMAL-PROTEIN ACCUMULATION [J].
NAM, HG ;
FRIED, HM .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1535-1544