Pex35 is a regulator of peroxisome abundance

  • Ido Yofe
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Kareem Soliman
    University Medical Center 2 Department of Child and Adolescent Health , , Göttingen 37075 , Germany
  • Silvia G. Chuartzman
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Bruce Morgan
    University of Kaiserslautern 3 Department of Cellular Biochemistry , , Kaiserslautern 67653 , Germany
  • Uri Weill
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Eden Yifrach
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Tobias P. Dick
    ZMBH-DKFZ Alliance, German Cancer Research Center (DKFZ) 4 Division of Redox Regulation , , Heidelberg 69121 , Germany
  • Sara J. Cooper
    HudsonAlpha Institute for Biotechnology 5 , Huntsville, AL 35806 , USA
  • Christer S. Ejsing
    VILLUM Center for Bioanalytical Sciences, University of Southern Denmark 6 Department of Biochemistry and Molecular Biology , , Odense 5230 , Denmark
  • Maya Schuldiner
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Einat Zalckvar
    Weizmann Institute of Science 1 Department of Molecular Genetics , , Rehovot 7610001 , Israel
  • Sven Thoms
    University Medical Center 2 Department of Child and Adolescent Health , , Göttingen 37075 , Germany

書誌事項

公開日
2017-02-15
権利情報
  • http://www.biologists.com/user-licence-1-1/
DOI
  • 10.1242/jcs.187914
公開者
The Company of Biologists

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説明

<jats:title>ABSTRACT</jats:title> <jats:p>Peroxisomes are cellular organelles with vital functions in lipid, amino acid and redox metabolism. The cellular formation and dynamics of peroxisomes are governed by PEX genes; however, the regulation of peroxisome abundance is still poorly understood. Here, we use a high-content microscopy screen in Saccharomyces cerevisiae to identify new regulators of peroxisome size and abundance. Our screen led to the identification of a previously uncharacterized gene, which we term PEX35, which affects peroxisome abundance. PEX35 encodes a peroxisomal membrane protein, a remote homolog to several curvature-generating human proteins. We systematically characterized the genetic and physical interactome as well as the metabolome of mutants in PEX35, and we found that Pex35 functionally interacts with the vesicle-budding-inducer Arf1. Our results highlight the functional interaction between peroxisomes and the secretory pathway.</jats:p>

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