Genetic variations in NADPH-CYP450 oxidoreductase in a Czech Slavic cohort

Author:

Tomková Mária1,Panda Satya Prakash2,Šeda Ondřej3,Baxová Alice3,Hůlková Martina1,Siler Masters Bettie Sue2,Martásek Pavel1

Affiliation:

1. Department of Pediatrics, First Faculty of Medicine, Charles University, 128 08 Prague, Czech Republic

2. Department of Biochemistry, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA

3. Institute of Biology & Medical Genetics, First Faculty of Medicine, Charles University, 12800 Prague, Czech Republic

Abstract

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

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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