Počet záznamů: 1  

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

  1. 1.
    SYSNO ASEP0425640
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevTranslation Initiation Factors eIF3 and HCR1 Control Translation Termination and Stop Codon Read-Through in Yeast Cells
    Tvůrce(i) 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
    Zdroj.dok.PLoS Genetics. - : Public Library of Science - ISSN 1553-7404
    Roč. 9, č. 11 (2013)
    Poč.str.17 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaRNA RECOGNITION MOTIF ; MESSENGER-RNA ; IN-VIVO
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEPGBP305/12/G034 GA ČR - Grantová agentura ČR
    Institucionální podporaMBU-M - RVO:61388971
    UT WOS000330369000042
    DOI10.1371/journal.pgen.1003962
    AnotaceTranslation 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
    PracovištěMikrobiologický ústav
    KontaktEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Rok sběru2014
Počet záznamů: 1  

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