mRNA decay is regulated via sequestration of the conserved 5'-3' exoribonuclease Xrn1 at eisosome in yeast
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28501103
DOI
10.1016/j.ejcb.2017.05.001
PII: S0171-9335(17)30025-0
Knihovny.cz E-zdroje
- Klíčová slova
- Eisosome, Pil1, Plasma membrane compartmentalization, Saccharomyces cerevisiae, Xrn1, mRNA decay regulation,
- 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
- Názvy látek
- exoribonukleasy MeSH
- fosfoproteiny MeSH
- membránové proteiny MeSH
- messenger RNA MeSH
- multiproteinové komplexy MeSH
- PIL1 protein, S cerevisiae MeSH Prohlížeč
- Saccharomyces cerevisiae - proteiny MeSH
- XRN1 protein, S cerevisiae MeSH Prohlížeč
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
Conserved mechanism of Xrn1 regulation by glycolytic flux and protein aggregation
Live cell fluorescence microscopy-an end-to-end workflow for high-throughput image and data analysis
Microdomain Protein Nce102 Is a Local Sensor of Plasma Membrane Sphingolipid Balance
Plasma Membrane Protein Nce102 Modulates Morphology and Function of the Yeast Vacuole
Role of MCC/Eisosome in Fungal Lipid Homeostasis
Long Noncoding RNAs in Yeast Cells and Differentiated Subpopulations of Yeast Colonies and Biofilms