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Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders
Author(s): Chang CC, Lee WH, Moser H, Valle D, Gould SJ
Source: NATURE GENETICS    Volume: 15    Issue: 4    Pages: 385-388    Published: APR 1997  
Times Cited: 110     References: 19     
Abstract: The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous diseases lethal in early infancy(1). Although the clinical features of PBD patients may vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins. This cellular phenotype is shared by yeast per mutants, and human orthologues of yeast PEX genes have been shown to be defective in some groups of PBD patients(2,3). We identified a putative human orthologue of ScPEX12 by screening the database of expressed sequence tags for cDNAs capable of encoding a protein similar to yeast Pex12p(4). Although its sequence similarity to yeast Pex12 proteins was limited. PEX12 shared the same subcellular distribution as yeast Pex12p and localized to the peroxisome membrane. PEX12 expression restored peroxisomal protein import in fibroblasts from PBD patients of complement group 3 (CG3) and frameshift mutations in PEX12 were detected in two unrelated CG3 patients. These data demonstrate that mutations in PEX12 are responsible for CG3 of the PBD and that PEX12 plays an essential role in peroxisomal matrix protein import.
Document Type: Article
Language: English
Addresses:
1. JOHNS HOPKINS UNIV, SCH MED, DEPT BIOL CHEM, BALTIMORE, MD 21205 USA
2. JOHNS HOPKINS UNIV, SCH MED, KENNEDY KRIEGER INST, BALTIMORE, MD 21205 USA
3. JOHNS HOPKINS UNIV, SCH MED, HOWARD HUGHES MED INST, BALTIMORE, MD 21205 USA
4. JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
5. JOHNS HOPKINS UNIV, SCH MED, DEPT ANAT & CELL BIOL, BALTIMORE, MD 21205 USA
Publisher: NATURE PUBLISHING CO, 345 PARK AVE SOUTH, NEW YORK, NY 10010-1707
Subject Category: Genetics & Heredity
IDS Number: WQ389
ISSN: 1061-4036
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