| Literature DB >> 14981078 |
Marleen Otzen1, Uta Perband, Dongyuan Wang, Richard J S Baerends, Wolf H Kunau, Marten Veenhuis, Ida J Van der Klei.
Abstract
We have cloned and characterized the Hansenula polymorpha PEX19 gene. In cells of a pex19 disruption strain (Hppex19), induced on methanol, peroxisome structures were not detectable; peroxisomal matrix proteins accumulated in the cytosol, whereas peroxisomal membrane proteins (PMPs) were mislocalized to the cytosol (Pex3p) and mitochondria (Pex14p) or strongly reduced to undetectable levels (Pex10p). The defect in peroxisome formation in Hppex19 cells was largely suppressed upon overproduction of HpPex3p or a fusion protein that consisted of the first 50 N-terminal amino acids of Pex3p and GFP. In these cells PMPs were again correctly sorted to peroxisomal structures, which also harbored peroxisomal matrix proteins. In Saccharomyces cerevisiae pex19 cells overproduction of ScPex3p led to the formation of numerous vesicles that contained PMPs but lacked the major matrix protein thiolase. Taken together, our data are consistent with a function of Pex19p in membrane protein assembly and function.Entities:
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Year: 2004 PMID: 14981078 DOI: 10.1074/jbc.M314275200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157