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Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G

Muntau, AC, Mayerhofer, PU, Paton, BC, Kammerer, S and Roscher, AA (2000) Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G Am J Hum Genet, 67. pp. 967-975.

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Abstract

Zellweger cerebro-hepato-renal syndrome is a severe congenital disorder associated with defective peroxisomal biogenesis. At least 23 PEX genes have been reported to be essential for peroxisome biogenesis in various species, indicating the complexity of peroxisomal assembly. Cells from patients with peroxisomal biogenesis disorders have previously been shown to segregate into >/=12 complementation groups. Two patients assigned to complementation group G who had not been linked previously to a specific gene defect were confirmed as displaying a cellular phenotype characterized by a lack of even residual peroxisomal membrane structures. Here we demonstrate that this complementation group is associated with mutations in the PEX3 gene, encoding an integral peroxisomal membrane protein. Homozygous PEX3 mutations, each leading to C-terminal truncation of PEX3, were identified in the two patients, who both suffered from a severe Zellweger syndrome phenotype. One of the mutations involved a single-nucleotide insertion in exon 7, whereas the other was a single-nucleotide substitution eight nucleotides from the normal splice site in the 3' acceptor site of intron 10. Expression of wild-type PEX3 in the mutant cell lines restored peroxisomal biogenesis, whereas transfection of mutated PEX3 cDNA did not. This confirmed that the causative gene had been identified. The observation of peroxisomal formation in the absence of morphologically recognizable peroxisomal membranes challenges the theory that peroxisomes arise exclusively by growth and division from preexisting peroxisomes and establishes PEX3 as a key factor in early human peroxisome synthesis.

Item Type: Article
Authors :
NameEmailORCID
Muntau, ACUNSPECIFIEDUNSPECIFIED
Mayerhofer, PUp.mayerhofer@surrey.ac.ukUNSPECIFIED
Paton, BCUNSPECIFIEDUNSPECIFIED
Kammerer, SUNSPECIFIEDUNSPECIFIED
Roscher, AAUNSPECIFIEDUNSPECIFIED
Date : 2000
Identification Number : 10.1086/303071
Uncontrolled Keywords : Amino Acid Sequence Base Sequence Cell Fusion DNA Mutational Analysis Exons/genetics Fibroblasts Fluorescent Antibody Technique *Genetic Complementation Test Humans Hybrid Cells/metabolism/pathology Infant Infant, Newborn Intracellular Membranes/metabolism/*pathology Introns/genetics Lipoproteins/chemistry/*genetics/metabolism Male Membrane Proteins/chemistry/*genetics/metabolism Mutation/*genetics Peroxisomes/metabolism/*pathology Protein Binding Transfection Zellweger Syndrome/classification/*genetics/*pathology/physiopathology
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 10:42
Last Modified : 17 May 2017 14:51
URI: http://epubs.surrey.ac.uk/id/eprint/828859

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