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

• Published in: Journal of cell science Vol. 123; no. 19; pp. 3389 - 3400
• Main Authors: Koch, Johannes, Pranjic, Kornelija, Huber, Anja, Ellinger, Adolf, Hartig, Andreas, Kragler, Friedrich, Brocard, Cécile
• Format: Journal Article
• Language: English
• Published: England The Company of Biologists Limited 01.10.2010
• Subjects: Cell Surface Extensions - metabolism; Cell Surface Extensions - pathology; Dynamins; Genetic Engineering; GTP Phosphohydrolases - metabolism; HEK293 Cells; Humans; Membrane Proteins - genetics; Membrane Proteins - metabolism; Microtubule-Associated Proteins - metabolism; Microtubules - metabolism; Mitochondrial Proteins - metabolism; Nicotiana; Peroxisomes - metabolism; Peroxisomes - pathology; Protein Binding; Protein Multimerization; Recombinant Fusion Proteins - genetics; Recombinant Fusion Proteins - metabolism; RNA, Small Interfering - genetics; Saccharomyces cerevisiae
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.064907

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.