Peroxisomal Membrane Fusion Requires Two Aaa Family Atpases, Pex1p and Pex6p
Open Access
- 21 August 2000
- journal article
- Published by Rockefeller University Press in Journal of Cell Biology
- Vol. 150 (4) , 881-886
Abstract
Two AAA family ATPases, NSF and p97, have been implicated in membrane fusion during assembly and inheritance of organelles of the secretory pathway. We have now investigated the roles of AAA ATPases in membrane fusion during assembly of the peroxisome, an organelle outside the classical secretory system. Here, we show that peroxisomal membrane fusion in the yeast Yarrowia lipolytica requires two AAA ATPases, Pex1p and Pex6p. Release of membrane- associated Pex1p and Pex6p drives the asymmetric priming of two fusion partners. The next step, peroxisome docking, requires release of Pex1p from one partner. Subsequent fusion of the peroxisomal membranes is independent of both Pex1p and Pex6p.Keywords
This publication has 28 references indexed in Scilit:
- Membrane Fusion and ExocytosisAnnual Review of Biochemistry, 1999
- Homotypic vacuolar fusion mediated by t- and v-SNAREsNature, 1997
- Docking of Yeast Vacuoles Is Catalyzed by the Ras-like GTPase Ypt7p after Symmetric Priming by Sec18p (NSF)Journal of Cell Biology, 1997
- Pay32p of the yeast Yarrowia lipolytica is an intraperoxisomal component of the matrix protein translocation machinery.Journal of Cell Biology, 1995
- The formation of golgi stacks from vesiculated golgi membranes requires two distinct fusion eventsCell, 1995
- Role of the PAS1 gene of Pichia pastoris in peroxisome biogenesis.Journal of Cell Biology, 1994
- Mechanisms of intracellular protein transportNature, 1994
- N-ethylmaleimide-sensitive fusion protein: a trimeric ATPase whose hydrolysis of ATP is required for membrane fusion.Journal of Cell Biology, 1994
- Cloning and characterization of PAS5: a gene required for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris.Journal of Cell Biology, 1993
- Distinct biochemical requirements for the budding, targeting, and fusion of ER-derived transport vesicles.Journal of Cell Biology, 1991