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

Zellweger cerebro-hepato-renal syndrome is a severe congenital disorder ass ociated with defective peroxisomal biogenesis. At least 23 PEX genes have b een 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 in to greater than or equal to 12 complementation groups. Two patients assigne d to complementation group G who had not been linked previously to a specif ic gene defect were confirmed as displaying a cellular phenotype characteri zed by a lack of even residual peroxisomal membrane structures. Here we dem onstrate that this complementation group is associated with mutations in th e PEX3 gene, encoding an integral peroxisomal membrane protein. Homozygous PEX3 mutations, each leading to C-terminal truncation of PEX3, were identif ied 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 nucleo tides from the normal splice site in the 3' acceptor site of intron 10, Exp ression of wild-type PEX3 in the mutant cell lines restored peroxisomal bio genesis, 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 membr anes 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.