Počet záznamů: 1  

Yeast phospholipase C is required for stability of casein kinase I Yck2p and expression of hexose transporters

  1. 1.
    SYSNO ASEP0483264
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevYeast phospholipase C is required for stability of casein kinase I Yck2p and expression of hexose transporters
    Tvůrce(i) Zhang, T. (US)
    Galdieri, L. (US)
    Hašek, Jiří (MBU-M) RID, ORCID
    Vančura, A. (US)
    Číslo článkufnx227
    Zdroj.dok.FEMS Microbiology Letters. - : Oxford University Press - ISSN 0378-1097
    Roč. 364, č. 22 (2017)
    Poč.str.8 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovaphospholipase C ; casein kinase I ; hexose transporters
    Vědní obor RIVEE - Mikrobiologie, virologie
    Obor OECDMicrobiology
    CEPGA16-05497S GA ČR - Grantová agentura ČR
    Institucionální podporaMBU-M - RVO:61388971
    UT WOS000416731600010
    DOI10.1093/femsle/fnx227
    AnotacePhospholipase C (Plc1p) in Saccharomyces cerevisiae is required for normal degradation of repressor Mth1p and expression of the HXT genes encoding cell membrane transporters of glucose. Plc1p is also required for normal localization of glucose transporters to the cell membrane. Consequently, plc1 Delta cells display histone hypoacetylation and transcriptional defects due to reduced uptake and metabolism of glucose to acetyl-CoA, a substrate for histone acetyltransferases. In the presence of glucose, Mth1p is phosphorylated by casein kinase I Yck1/2p, ubiquitinated by the SCFGrr1 complex and degraded by the proteasome. Here, we show that while Plc1p does not affect the function of the SCFGrr1 complex or the proteasome, it is required for normal protein level of Yck2p. Since stability of Yck1/2p is regulated by a glucose-dependent mechanism, PLC1 inactivation results in destabilization of Yck1/2p and defect in Mth1p degradation. Based on our results and published data, we propose a model in which plc1 Delta mutation causes increased internalization of glucose transporters, decreased transport of glucose into the cells, and consequently decreased stability of Yck1/2p, increased stability of Mth1p and decreased expression of the HXT genes.
    PracovištěMikrobiologický ústav
    KontaktEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Rok sběru2018
Počet záznamů: 1  

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