Abstract
CYP3, the gene which encodes the hepatic cytochrome P450pcn1, the isozyme responsible for the metabolic oxidation of the calcium channel-blocking drug nifedipine, has recently been mapped to human chromosome 7 using somatic cell hybrids. Using multilocus linkage analysis in CEPH families, we examined the linkage of a cDNA probe (hPCN1) for CYP3 to the oncogene MET, the pro-alpha 2(1) collagen gene COL1A2, and the T-cell receptor beta-chain gene TCRB, together with three arbitrary loci D7S8, D7S13, and D7S16, defined by the anonymous DNA probes pJ3.11, pB79a, and p7C22, respectively. From 70 CEPH parents screened with a StyI RFLP for hPCN1, four informative families were found each with both parental and maternal grandparents and 6-11 children per family. Tight linkage emerged between CYP3 and COL1A2, with a maximum combined lod score of 5.72 at theta = 0, suggesting the most likely subchromosomal localization of CYP3 is 7q21.3-q22.1.
Original language | English |
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Pages (from-to) | 280-4 |
Number of pages | 5 |
Journal | American Journal of Human Genetics |
Volume | 43 |
Issue number | 3 |
Publication status | Published - Sept 1988 |
Keywords
- Chromosomes, Human, Pair 7
- Cloning, Molecular
- Collagen
- Cytochrome P-450 CYP3A
- Cytochrome P-450 Enzyme System
- Female
- Genetic Linkage
- Humans
- Male
- Mixed Function Oxygenases
- Nifedipine
- Pedigree
- Polymorphism, Restriction Fragment Length