Genetic variations in NADPH-CYP450 oxidoreductase in a Czech Slavic cohort
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 GM081568
NIGMS NIH HHS - United States
US NIH GM081568
NIGMS NIH HHS - United States
PubMed
25712184
PubMed Central
PMC4662547
DOI
10.2217/pgs.14.169
Knihovny.cz E-resources
- Keywords
- CYP, Czech Slavic population, NADPH-cytochrome, P450 oxidoreductase, P450 reductase, POR, allele frequencies, haplotype, pharmacogenetics,
- MeSH
- DNA genetics MeSH
- Adult MeSH
- Gene Frequency MeSH
- Genetic Variation MeSH
- Haplotypes MeSH
- Polymorphism, Single Nucleotide * MeSH
- Kinetics MeSH
- Cohort Studies MeSH
- Protein Conformation MeSH
- Humans MeSH
- Mutation, Missense MeSH
- Models, Molecular MeSH
- Infant, Newborn MeSH
- Base Sequence MeSH
- Amino Acid Substitution MeSH
- Cytochrome P-450 Enzyme System chemistry genetics metabolism MeSH
- Linkage Disequilibrium MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- DNA MeSH
- POR protein, human MeSH Browser
- Cytochrome P-450 Enzyme System MeSH
AIM: Estimating polymorphic allele frequencies of the NADPH-CYP450 oxidoreductase (POR) gene in a Czech Slavic population. METHODS: The POR gene was analyzed in 322 individuals from a control cohort by sequencing and high resolution melting analysis. RESULTS: We identified seven unreported SNP genetic variations, including two SNPs in the 5' flanking region (g.4965C>T and g.4994G>T), one intronic variant (c.1899-20C>T), one synonymous SNP (p.20Ala=) and three nonsynonymous SNPs (p.Thr29Ser, p.Pro384Leu and p.Thr529Met). The p.Pro384Leu variant exhibited reduced enzymatic activities compared with wild-type. CONCLUSION: New POR variant identification indicates the number of uncommon variants might be specific for each subpopulation being investigated, particularly germane to the singular role that POR plays in providing reducing equivalents to all CYP450s in the endoplasmic reticulum. Original submitted 15 September 2014; Revision submitted 17 November 2014.
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