期刊
JOURNAL OF CELL BIOLOGY
卷 149, 期 7, 页码 1345-1359出版社
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.149.7.1345
关键词
Zellweger syndrome; membrane biogenesis; protein import; vesicle traffic; peroxisome biogenesis disorders
类别
资金
- NICHD NIH HHS [P01 HD010981, HD10981] Funding Source: Medline
- NIDDK NIH HHS [R01 DK045787, DK45787] Funding Source: Medline
In humans, defects in peroxisome biogenesis are the cause of lethal diseases typified by Zellweger syndrome. Here, we show that inactivating mutations in human PEX3 cause Zellweger syndrome, abrogate peroxisome membrane synthesis, and result in reduced abundance of peroxisomal membrane proteins (PMPs) and/or mislocalization of PMPs to the mitochondria. Previous studies have suggested that PEX3 may traffic through the ER en route to the peroxisome, that the COPI inhibitor, brefeldin A, leads to accumulation of PEX3 in the ER, and that PEX3 overexpression alters the morphology of the ER. However, we were unable to detect PEX3 in the ER at early times after expression. Furthermore, we find that inhibition of COPI function by brefeldin A has no effect on trafficking of PEX3 to peroxisomes and does not inhibit PEX3-mediated peroxisome biogenesis. We also find that inhibition of COPII-dependent membrane traffic by a dominant negative SAR1 mutant fails to block PEX3 transport to peroxisomes and PEX3-mediated peroxisome synthesis. Based on these results, we propose that PEX3 targeting to peroxisomes and PEX3-mediated peroxisome membrane synthesis may occur independently of COPI- and COPII-dependent membrane traffic.
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