EVIDENCE FOR FREQUENT GENE CONVERSION IN THE STEROID 21-HYDROXYLASE P-450(C21) GENE - IMPLICATIONS FOR STEROID 21-HYDROXYLASE DEFICIENCY

Google Scholar
  • 1 January 1988
    • journal article
    • research article
    • Vol. 42  (1) , 17-25
Abstract
Oligonucleotide probes specific for the deleterious mutations harbored in the P-450 (C21)A pseudogene and oligonucleotide probes specific for the corresponding sequences in the B gene were prepared to examine the molecular lesions in the P-450(C21) gene of P-450(C21)-deficient patients. Using these gene-specific probes, we performed Southern blot analyses of genomic DNAs from 11 patients and eight normal individuals. At least one allele of the B gene (the 3.7-kb TaqI fragment) in a patient was inactivated by mutations caused by recombination with the A gene. The A genes in normal individuals and patients seemed to be replaced frequently (i.e., 10/19 individuals) in their 3'' portions by B gene sequences. All of these alterations occurred without changing the characteristic length (3.2kb) of the TaqI fragment of the A gene, a result strongly suggesting that frequent gene conversions and/or intragenic recombinations have happened in the P-450(C21) genes. Densitometric analysis of the autoradiograms from hybridization experiments revealed extensive variation (from one to five copies) in the copy number of the A gene (the 3.2-kb TaqI fragment) whereas that of the B gene (the 3.7-kb TaqI fragment) was relatively constant at two or three copies.