Pex35 is a regulator of peroxisome abundance

Author:

Yofe Ido1,Soliman Kareem2,Chuartzman Silvia G.1,Morgan Bruce34,Weill Uri1,Yifrach Eden1,Dick Tobias P.4,Cooper Sara J.5,Ejsing Christer S.6,Schuldiner Maya1,Zalckvar Einat1,Thoms Sven2ORCID

Affiliation:

1. Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 7610001, Israel

2. Department of Child and Adolescent Health, University Medical Center, 37075 Göttingen, Germany

3. Department of Cellular Biochemistry, University of Kaiserslautern, 67653 Kaiserslautern, Germany

4. Division of Redox Regulation, ZMBH-DKFZ Alliance, German Cancer Research Center (DKFZ), 69121 Heidelberg, Germany

5. HudsonAlpha Institute for Biotechnology, Huntsville, Alabama 35806, USA

6. Department of Biochemistry and Molecular Biology, VILLUM Center for Bioanalytical Sciences, University of Southern Denmark, 5230 Odense, Denmark

Abstract

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 yet poorly understood. Here we use a high-content microscopy screen to identify novel 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.

Funder

State of Lower-Saxony, Hannover, Germany

European Research Council

Publisher

The Company of Biologists

Subject

Cell Biology

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