Literature DB >> 10445880

Overexpression of truncated Nmd3p inhibits protein synthesis in yeast.

J P Belk1, F He, A Jacobson.   

Abstract

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 nmd3delta100 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.

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Year:  1999        PMID: 10445880      PMCID: PMC1369829          DOI: 10.1017/s1355838299990027

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  56 in total

Review 1.  Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells.

Authors:  A Jacobson; S W Peltz
Journal:  Annu Rev Biochem       Date:  1996       Impact factor: 23.643

2.  RRP5 is required for formation of both 18S and 5.8S rRNA in yeast.

Authors:  J Venema; D Tollervey
Journal:  EMBO J       Date:  1996-10-15       Impact factor: 11.598

3.  Yeast virus propagation depends critically on free 60S ribosomal subunit concentration.

Authors:  Y Ohtake; R B Wickner
Journal:  Mol Cell Biol       Date:  1995-05       Impact factor: 4.272

4.  An essential component of the decapping enzyme required for normal rates of mRNA turnover.

Authors:  C A Beelman; A Stevens; G Caponigro; T E LaGrandeur; L Hatfield; D M Fortner; R Parker
Journal:  Nature       Date:  1996-08-15       Impact factor: 49.962

5.  Identification of an additional gene required for eukaryotic nonsense mRNA turnover.

Authors:  B S Lee; M R Culbertson
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

6.  The majority of yeast UPF1 co-localizes with polyribosomes in the cytoplasm.

Authors:  A L Atkin; N Altamura; P Leeds; M R Culbertson
Journal:  Mol Biol Cell       Date:  1995-05       Impact factor: 4.138

7.  Identification and characterization of mutations in the UPF1 gene that affect nonsense suppression and the formation of the Upf protein complex but not mRNA turnover.

Authors:  Y Weng; K Czaplinski; S W Peltz
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

8.  Turnover mechanisms of the stable yeast PGK1 mRNA.

Authors:  D Muhlrad; C J Decker; R Parker
Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

9.  Interaction between Nmd2p and Upf1p is required for activity but not for dominant-negative inhibition of the nonsense-mediated mRNA decay pathway in yeast.

Authors:  F He; A H Brown; A Jacobson
Journal:  RNA       Date:  1996-02       Impact factor: 4.942

10.  Purification and characterization of the Upf1 protein: a factor involved in translation and mRNA degradation.

Authors:  K Czaplinski; Y Weng; K W Hagan; S W Peltz
Journal:  RNA       Date:  1995-08       Impact factor: 4.942

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  22 in total

1.  Nascent 60S ribosomal subunits enter the free pool bound by Nmd3p.

Authors:  J H Ho; G Kallstrom; A W Johnson
Journal:  RNA       Date:  2000-11       Impact factor: 4.942

2.  Eukaryote-specific domains in translation initiation factors: implications for translation regulation and evolution of the translation system.

Authors:  L Aravind; E V Koonin
Journal:  Genome Res       Date:  2000-08       Impact factor: 9.043

3.  Ribosomal protein L33 is required for ribosome biogenesis, subunit joining, and repression of GCN4 translation.

Authors:  Pilar Martín-Marcos; Alan G Hinnebusch; Mercedes Tamame
Journal:  Mol Cell Biol       Date:  2007-06-04       Impact factor: 4.272

4.  Upf1p, Nmd2p, and Upf3p regulate the decapping and exonucleolytic degradation of both nonsense-containing mRNAs and wild-type mRNAs.

Authors:  F He; A Jacobson
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

5.  Dominant mutations in the late 40S biogenesis factor Ltv1 affect cytoplasmic maturation of the small ribosomal subunit in Saccharomyces cerevisiae.

Authors:  Claire A Fassio; Brett J Schofield; Robert M Seiser; Arlen W Johnson; Deborah E Lycan
Journal:  Genetics       Date:  2010-03-09       Impact factor: 4.562

6.  Ltv1 is required for efficient nuclear export of the ribosomal small subunit in Saccharomyces cerevisiae.

Authors:  Robert M Seiser; Alexandra E Sundberg; Bethany J Wollam; Pamela Zobel-Thropp; Katherine Baldwin; Maxwell D Spector; Deborah E Lycan
Journal:  Genetics       Date:  2006-08-03       Impact factor: 4.562

7.  Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p.

Authors:  O Gadal; D Strauss; J Kessl; B Trumpower; D Tollervey; E Hurt
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

8.  Ribosomal protein L35 is required for 27SB pre-rRNA processing in Saccharomyces cerevisiae.

Authors:  Reyes Babiano; Jesús de la Cruz
Journal:  Nucleic Acids Res       Date:  2010-04-14       Impact factor: 16.971

9.  The putative GTPases Nog1p and Lsg1p are required for 60S ribosomal subunit biogenesis and are localized to the nucleus and cytoplasm, respectively.

Authors:  George Kallstrom; John Hedges; Arlen Johnson
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

10.  Coordinated nuclear export of 60S ribosomal subunits and NMD3 in vertebrates.

Authors:  Christopher R Trotta; Elsebet Lund; Lawrence Kahan; Arlen W Johnson; James E Dahlberg
Journal:  EMBO J       Date:  2003-06-02       Impact factor: 11.598

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