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      Analysis of autophagy activated during changes in carbon source availability in yeast cells

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          Abstract

          Autophagy is a conserved intracellular degradation system in eukaryotes. Recent studies have revealed that autophagy can be induced not only by nitrogen starvation but also by many other stimuli. However, questions persist regarding the types of conditions that induce autophagy, as well as the particular kinds of autophagy that are induced under these specific conditions. In experimental studies, abrupt nutrient changes are often used to induce autophagy. In this study, we investigated autophagy induction in batch culture on low-glucose medium, in which growth of yeast ( Saccharomyces cerevisiae) cells is clearly reflected exclusively by carbon source state. In this medium, cells pass sequentially through three stages: glucose-utilizing, ethanol-utilizing, and ethanol-depleted phases. Using GFP cleavage assay by immunoblotting methods, fluorescence microscopy, and transmission electron microscopy ultrastructural analysis, we found that bulk autophagy and endoplasmic reticulum-phagy are induced starting at the ethanol-utilizing phase, and bulk autophagy is activated to a greater extent in the ethanol-depleted phase. Furthermore, we found that mitophagy is induced by ethanol depletion. Microautophagy occurred after glucose depletion and involved incorporation of cytosolic components and lipid droplets into the vacuolar lumen. Moreover, we observed that autophagy-deficient cells grow more slowly in the ethanol-utilizing phase and exhibit a delay in growth resumption when they are shifted to fresh medium from the ethanol-depleted phase. Our findings suggest that distinct types of autophagy are induced in yeast cells undergoing gradual changes in carbon source availability.

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          Author and article information

          Journal
          J Biol Chem
          J. Biol. Chem
          jbc
          jbc
          JBC
          The Journal of Biological Chemistry
          American Society for Biochemistry and Molecular Biology (11200 Rockville Pike, Suite 302, Rockville, MD 20852-3110, U.S.A. )
          0021-9258
          1083-351X
          5 April 2019
          12 February 2019
          : 294
          : 14
          : 5590-5603
          Affiliations
          [1]From the Cell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, 4259-S2-12 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan
          Author notes
          [1 ] To whom correspondence should be addressed: Cell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology, 4259-S2-12 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan. Tel.: 81-45-924-5113; Fax: 81-45-924-5121; E-mail: yohsumi@ 123456iri.titech.ac.jp .

          Edited by George N. DeMartino

          Article
          PMC6462502 PMC6462502 6462502 RA118.005698
          10.1074/jbc.RA118.005698
          6462502
          30755486
          81437134-4907-4d17-b8a9-34b35f2cc1e5
          © 2019 Iwama and Ohsumi.

          Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.

          History
          : 4 September 2018
          : 5 February 2019
          Funding
          Funded by: MEXT | Japan Society for the Promotion of Science (JSPS) , open-funder-registry 10.13039/501100001691;
          Award ID: JP23000015
          Award ID: JP16H06375
          Award ID: JP17K15245
          Award Recipient : Award Recipient :
          Categories
          Cell Biology

          mitophagy,glucose,ethanol,nutrient starvation,autophagy,yeast,physiology,autophagy-related protein 8 (Atg8),ER-phagy,diauxie

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