Literature DB >> 10440865

Should we kill the messenger? The role of the surveillance complex in translation termination and mRNA turnover.

K Czaplinski1, M J Ruiz-Echevarria, C I González, S W Peltz.   

Abstract

Eukaryotes have evolved conserved mechanisms to rid cells of faulty gene products that can interfere with cell function. mRNA surveillance is an example of a pathway that monitors the translation termination process and promotes degradation of transcripts harboring premature translation termination codons. Studies on the mechanism of mRNA surveillance in yeast and humans suggest a common mechanism where a "surveillance complex" monitors the translation process and determines whether translation termination has occurred at the correct position within the mRNA. A model will be presented that suggests that the surveillance complex assesses translation termination by monitoring the transition of an RNP as it is converted from a nuclear to a cytoplasmic form during the initial rounds of translation. Copyright 1999 John Wiley & Sons, Inc.

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Year:  1999        PMID: 10440865     DOI: 10.1002/(SICI)1521-1878(199908)21:8<685::AID-BIES8>3.0.CO;2-4

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  41 in total

1.  Recognition of yeast mRNAs as "nonsense containing" leads to both inhibition of mRNA translation and mRNA degradation: implications for the control of mRNA decapping.

Authors:  D Muhlrad; R Parker
Journal:  Mol Biol Cell       Date:  1999-11       Impact factor: 4.138

2.  Aberrant mRNAs with extended 3' UTRs are substrates for rapid degradation by mRNA surveillance.

Authors:  D Muhlrad; R Parker
Journal:  RNA       Date:  1999-10       Impact factor: 4.942

3.  Splicing and 3' end formation in the definition of nonsense-mediated decay-competent human beta-globin mRNPs.

Authors:  G Neu-Yilik; N H Gehring; R Thermann; U Frede; M W Hentze; A E Kulozik
Journal:  EMBO J       Date:  2001-02-01       Impact factor: 11.598

4.  The Y14 protein communicates to the cytoplasm the position of exon-exon junctions.

Authors:  V N Kim; J Yong; N Kataoka; L Abel; M D Diem; G Dreyfuss
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

5.  Kinetics of ribosomal pausing during programmed -1 translational frameshifting.

Authors:  J D Lopinski; J D Dinman; J A Bruenn
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

Review 6.  Upstream open reading frames as regulators of mRNA translation.

Authors:  D R Morris; A P Geballe
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

7.  Regulation of calpain and calpastatin in differentiating myoblasts: mRNA levels, protein synthesis and stability.

Authors:  S Barnoy; L Supino-Rosin; N S Kosower
Journal:  Biochem J       Date:  2000-10-15       Impact factor: 3.857

8.  Nonsense-mediated decay mutants do not affect programmed -1 frameshifting.

Authors:  L Bidou; G Stahl; I Hatin; O Namy; J P Rousset; P J Farabaugh
Journal:  RNA       Date:  2000-07       Impact factor: 4.942

9.  Complex regulation of the human gene for the Z-DNA binding protein DLM-1.

Authors:  Stefan Rothenburg; Thomas Schwartz; Friedrich Koch-Nolte; Friedrich Haag
Journal:  Nucleic Acids Res       Date:  2002-02-15       Impact factor: 16.971

10.  Mtt1 is a Upf1-like helicase that interacts with the translation termination factors and whose overexpression can modulate termination efficiency.

Authors:  K Czaplinski; N Majlesi; T Banerjee; S W Peltz
Journal:  RNA       Date:  2000-05       Impact factor: 4.942

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