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Dispersion of Endoplasmic Reticulum-associated Compartments by 4-phenyl Butyric Acid in Yeast Cells.
Mai, Thanh Chi; Ishiwata-Kimata, Yuki; Le, Quynh Giang; Kido, Hiroyuki; Kimata, Yukio.
Afiliación
  • Mai TC; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology.
  • Ishiwata-Kimata Y; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology.
  • Le QG; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology.
  • Kido H; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology.
  • Kimata Y; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology.
Cell Struct Funct ; 44(2): 173-182, 2019 Nov 23.
Article en En | MEDLINE | ID: mdl-31619600
In yeast Saccharomyces cerevisiae cells, some aberrant multimembrane-spanning proteins are not transported to the cell surface but form and are accumulated in endoplasmic reticulum (ER)-derived subcompartments, known as the ER-associated compartments (ERACs), which are observed as puncta under fluorescence microscopy. Here we show that a mutant of the cell surface protein Pma1, Pma1-2308, was accumulated in the ERACs, as well as the heterologously expressed mammalian cystic fibrosis transmembrane conductance regulator (CFTR), in yeast cells. Pma1-2308 and CFTR were located on the same ERACs. We also note that treatment of cells with 4-phenyl butyric acid (4-PBA) compromised the ERAC formation by Pma1-2308 and CFTR, suggesting that 4-PBA exerts a chaperone-like function in yeast cells. Intriguingly, unlike ER stress induced by the canonical ER stressor tunicamycin, ER stress that was induced by Pma1-2308 was aggravated by 4-PBA. We assume that this observation demonstrates a beneficial aspect of ERACs, and thus propose that the ERACs are formed through aggregation of aberrant transmembrane proteins and work as the accumulation sites of multiple ERAC-forming proteins for their sequestration.Key words: protein aggregation, organelle, unfolded protein response, ER stress, 4-PBA.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenilbutiratos / Saccharomyces cerevisiae / Retículo Endoplásmico Tipo de estudio: Risk_factors_studies Idioma: En Revista: Cell Struct Funct Año: 2019 Tipo del documento: Article Pais de publicación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenilbutiratos / Saccharomyces cerevisiae / Retículo Endoplásmico Tipo de estudio: Risk_factors_studies Idioma: En Revista: Cell Struct Funct Año: 2019 Tipo del documento: Article Pais de publicación: Japón