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Mitochondrial anchorage and fusion contribute to mitochondrial inheritance and quality control in the budding yeast Saccharomyces cerevisiae
Authors:Ryo Higuchi-Sanabria  Joseph K Charalel  Matheus P Viana  Enrique J Garcia  Cierra N Sing  Andrea Koenigsberg  Theresa C Swayne  Jason D Vevea  Istvan R Boldogh  Susanne M Rafelski  Liza A Pon
Institution:University of Colorado, Boulder;aDepartment of Pathology and Cell Biology, Columbia University, New York, NY 10032;cHerbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032;bDepartment of Developmental and Cell Biology and Center for Complex Biological Systems, University of California, Irvine, Irvine, CA 92697
Abstract:Higher-functioning mitochondria that are more reduced and have less ROS are anchored in the yeast bud tip by the Dsl1-family protein Mmr1p. Here we report a role for mitochondrial fusion in bud-tip anchorage of mitochondria. Fluorescence loss in photobleaching (FLIP) and network analysis experiments revealed that mitochondria in large buds are a continuous reticulum that is physically distinct from mitochondria in mother cells. FLIP studies also showed that mitochondria that enter the bud can fuse with mitochondria that are anchored in the bud tip. In addition, loss of fusion and mitochondrial DNA (mtDNA) by deletion of mitochondrial outer or inner membrane fusion proteins (Fzo1p or Mgm1p) leads to decreased accumulation of mitochondria at the bud tip and inheritance of fitter mitochondria by buds compared with cells with no mtDNA. Conversely, increasing the accumulation and anchorage of mitochondria in the bud tip by overexpression of MMR1 results in inheritance of less-fit mitochondria by buds and decreased replicative lifespan and healthspan. Thus quantity and quality of mitochondrial inheritance are ensured by two opposing processes: bud-tip anchorage by mitochondrial fusion and Mmr1p, which favors bulk inheritance; and quality control mechanisms that promote segregation of fitter mitochondria to the bud.
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