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Translation Initiation Factors eIF3 and HCR1 Control Translation Termination and Stop Codon Read-Through in Yeast Cells

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    SYSNO ASEP0425640
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTranslation Initiation Factors eIF3 and HCR1 Control Translation Termination and Stop Codon Read-Through in Yeast Cells
    Author(s) Beznosková, Petra (MBU-M) RID
    Cuchalová, Lucie (MBU-M)
    Wagner, Susan (MBU-M) RID, ORCID
    Shoemaker, Ch. J. (US)
    Gunišová, Stanislava (MBU-M) RID
    von der Haar, T. (GB)
    Valášek, Leoš Shivaya (MBU-M) RID, ORCID
    Source TitlePLoS Genetics. - : Public Library of Science - ISSN 1553-7404
    Roč. 9, č. 11 (2013)
    Number of pages17 s.
    Languageeng - English
    CountryUS - United States
    KeywordsRNA RECOGNITION MOTIF ; MESSENGER-RNA ; IN-VIVO
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGBP305/12/G034 GA ČR - Czech Science Foundation (CSF)
    Institutional supportMBU-M - RVO:61388971
    UT WOS000330369000042
    DOI10.1371/journal.pgen.1003962
    AnnotationTranslation is divided into initiation, elongation, termination and ribosome recycling. Earlier work implicated several eukaryotic initiation factors (eIFs) in ribosomal recycling in vitro. Here, we uncover roles for HCR1 and eIF3 in translation termination in vivo. A substantial proportion of eIF3, HCR1 and eukaryotic release factor 3 (eRF3) but not eIF5 (a well-defined "initiation-specific" binding partner of eIF3) specifically co-sediments with 80S couples isolated from RNase-treated heavy polysomes in an eRF1-dependent manner, indicating the presence of eIF3 and HCR1 on terminating ribosomes. eIF3 and HCR1 also occur in ribosome-and RNA-free complexes with both eRFs and the recycling factor ABCE1/RLI1. Several eIF3 mutations reduce rates of stop codon read-through and genetically interact with mutant eRFs. In contrast, a slow growing deletion of hcr1 increases read-through and accumulates eRF3 in heavy polysomes in a manner suppressible by overexpressed ABCE1/RLI1. Based on these and other findings we propose that upon stop codon recognition, HCR1 promotes eRF3.GDP ejection from the post-termination complexes to allow binding of its interacting partner ABCE1/RLI1
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2014
Number of the records: 1  

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