A MUTATION LOCATED AT THE 5-BETA SPLICE JUNCTION SEQUENCE OF INTRON-3 IN THE P67(PHOX) GENE CAUSES THE LACK OF P67(PHOX) MESSENGER-RNA IN A PATIENT WITH CHRONIC GRANULOMATOUS-DISEASE

Chronic granulomatous disease (CGD) is due to a functional defect of the O-2(-)-generating NADPH oxidase of neutrophils. Mutations resulting in CGD have been shown to occur in only four genes, thus identifying the main components of the oxidase complex, namely the two subunits of a membrane-bound cytochrome b and two cytosolic factors of activation of 67 kD (p67(phox)) and 47 kD (p47(phox)). The present study deals with the biochemical and genetic analysis of the defect in a patient suffering from a p67(phox)-deficient form of CGD. The p67(phox) deficiency was ascertained by immunochemistry and the ability of recombinant p67(phox) to restore NADPH oxidase activity using a cell-free system of oxidase activation. The cellular extracts from the proband contained no p67(phox) protein and no p67(phox) mRNA when assayed by Western and Northern blot analysis. However, reverse transcription of mRNA and subsequent cDNA amplification by polymerase chain reaction using specific p67(phox) primers showed that trace amounts of a p67(phox) mRNA deleted for exon 3 were synthesized in the patient immortalized B lymphocytes. Sequence analysis of the genomic DNA showed a T-to-C transition at position +2 of intron 3. This point mutation in the consensus 5' splice site of the intron 3 was probably responsible for lack of accumulation of mRNA and also for the skipping of exon 3 detected in the few mRNA molecules that escaped cellular degradation. (C) 1995 by The American Society of Hematology.