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mRNA decay is regulated via sequestration of the conserved 5'-3' exoribonuclease Xrn1 at eisosome in yeast
K. Vaškovičová, T. Awadová, P. Veselá, M. Balážová, M. Opekarová, J. Malinsky,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články
- MeSH
- buněčná membrána genetika metabolismus MeSH
- cytoplazma genetika metabolismus MeSH
- exoribonukleasy genetika metabolismus MeSH
- fosfoproteiny genetika metabolismus MeSH
- membránové mikrodomény genetika metabolismus MeSH
- membránové proteiny genetika metabolismus MeSH
- messenger RNA metabolismus MeSH
- multiproteinové komplexy genetika metabolismus MeSH
- Saccharomyces cerevisiae - proteiny genetika metabolismus MeSH
- Saccharomyces cerevisiae genetika metabolismus MeSH
- stabilita RNA genetika MeSH
- Publikační typ
- časopisecké články MeSH
We describe a novel mechanism of mRNA decay regulation, which takes place under the conditions of glucose deprivation in the yeast Saccharomyces cerevisiae. The regulation is based on temporally stable sequestration of the main 5'-3' mRNA exoribonuclease Xrn1 at the eisosome, a plasma membrane-associated protein complex organizing a specialized membrane microdomain. As documented by monitoring the decay of a specific mRNA substrate in time, Xrn1-mediated mRNA degradation ceases during the accumulation of Xrn1 at eisosome, but the eisosome-associated Xrn1 retains its functionality and can be re-activated when released to cytoplasm following the addition of glucose. In cells lacking the eisosome organizer Pil1, Xrn1 does not associate with the plasma membrane and its activity is preserved till the stationary phase. Thus, properly assembled eisosome is necessary for this kind of Xrn1 regulation, which occurs in a liquid culture as well as in a differentiated colony.
Citace poskytuje Crossref.org
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