Affiliation:
1. Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, 1 and
2. Integrated Imaging Center, Department of Biology, The Johns Hopkins University, Baltimore, Maryland 212182
Abstract
ABSTRACT
Peroxisomes are independent organelles found in virtually all eukaryotic cells. Genetic studies have identified more than 20
PEX
genes that are required for peroxisome biogenesis. The role of most
PEX
gene products, peroxins, remains to be determined, but a variety of studies have established that Pex5p binds the type 1 peroxisomal targeting signal and is the import receptor for most newly synthesized peroxisomal matrix proteins. The steady-state abundance of Pex5p is unaffected in most
pex
mutants of the yeast
Pichia pastoris
but is severely reduced in
pex4
and
pex22
mutants and moderately reduced in
pex1
and
pex6
mutants. We used these subphenotypes to determine the epistatic relationships among several groups of
pex
mutants. Our results demonstrate that Pex4p acts after the peroxisome membrane synthesis factor Pex3p, the Pex5p docking factors Pex13p and Pex14p, the matrix protein import factors Pex8p, Pex10p, and Pex12p, and two other peroxins, Pex2p and Pex17p. Pex22p and the interacting AAA ATPases Pex1p and Pex6p were also found to act after Pex10p. Furthermore, Pex1p and Pex6p were found to act upstream of Pex4p and Pex22p. These results suggest that Pex1p, Pex4p, Pex6p, and Pex22p act late in peroxisomal matrix protein import, after matrix protein translocation. This hypothesis is supported by the phenotypes of the corresponding mutant strains. As has been shown previously for
P. pastoris pex1
,
pex6
, and
pex22
mutant cells, we show here that
pex4Δ
mutant cells contain peroxisomal membrane protein-containing peroxisomes that import residual amounts of peroxisomal matrix proteins.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
143 articles.
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