PEX11 family members are membrane elongation factors that coordinate peroxisome proliferation and maintenance

Author:

Koch Johannes1,Pranjic Kornelija1,Huber Anja1,Ellinger Adolf2,Hartig Andreas1,Kragler Friedrich1,Brocard Cécile1

Affiliation:

1. Max F. Perutz Laboratories, Center of Molecular Biology, University of Vienna, Department of Biochemistry and Cell Biology, Dr Bohr-Gasse 9, 1030, Vienna, Austria

2. Department of Cell Biology and Ultrastructure Research, Center for Anatomy and Cell Biology, Medical University of Vienna, Schwarzspanierstrasse 17, 1090, Vienna, Austria

Abstract

Dynamic changes of membrane structure are intrinsic to organelle morphogenesis and homeostasis. Ectopic expression of proteins of the PEX11 family from yeast, plant or human lead to the formation of juxtaposed elongated peroxisomes (JEPs),which is evocative of an evolutionary conserved function of these proteins in membrane tubulation. Microscopic examinations reveal that JEPs are composed of independent elongated peroxisomes with heterogeneous distribution of matrix proteins. We established the homo- and heterodimerization properties of the human PEX11 proteins and their interaction with the fission factor hFis1, which is known to recruit the GTPase DRP1 to the peroxisomal membrane. We show that excess of hFis1 but not of DRP1 is sufficient to fragment JEPs into normal round-shaped organelles, and illustrate the requirement of microtubules for JEP formation. Our results demonstrate that PEX11-induced JEPs represent intermediates in the process of peroxisome membrane proliferation and that hFis1 is the limiting factor for progression. Hence, we propose a model for a conserved role of PEX11 proteins in peroxisome maintenance through peroxisome polarization, membrane elongation and segregation.

Publisher

The Company of Biologists

Subject

Cell Biology

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