Hart Steven N, Li Ye, Nakamoto Kaori, Wesselman Chris, Zhong Xiao-bo
Department of Pharmacology, Toxicology, and Therapeutics, The University of Kansas Medical Center, KS 66160, USA.
Drug Metab Pharmacokinet. 2007 Aug;22(4):322-6. doi: 10.2133/dmpk.22.322.
Cytochrome P450 oxidoreductase (POR) is the single flavoprotein which donates electrons to the microsomal cytochrome P450 enzymes for oxidation of their substrates. In this study, we sequenced all 15 exons and the surrounding intronic sequences of POR in 100 human liver samples to identify novel and confirm known genetic polymorphisms in POR. Thirty-four single nucleotide polymorphisms (SNPs) were identified including 9 in the coding exons (5 synonymous and 4 nonsynonymous), 20 in the intronic regions, and 5 in the 3'-UTR. Of these, 9 were novel SNPs, including three nonsynonymous SNPs, SNH313003 (817733G>C; K49N), SNH313020 (848661C>A; L420M), and SNH313029 (849577T>C; L577P) with minor allele frequencies of 0.005, 0.045, and 0.020, respectively. We also confirmed a previously reported non-synonymous SNP rs1057868 (A503V) as well as five synonymous SNPs (G5G, T29T, P129P, S485S, and S572S) all with allele frequencies similar to those previously reported. Structurally, these polymorphisms occur in different regions: SNH313003 (K49N) in the amino-terminal tail, SNH313020 (L420M) in the connecting domain, SNH313029 (L577P) in the NADPH-binding domain, and rs1057868 (A503V) in the FAD binding domain.
细胞色素P450氧化还原酶(POR)是一种单一的黄素蛋白,它将电子传递给微粒体细胞色素P450酶,用于氧化其底物。在本研究中,我们对100份人类肝脏样本中POR的所有15个外显子及其周围的内含子序列进行了测序,以鉴定POR中的新遗传多态性并确认已知的遗传多态性。共鉴定出34个单核苷酸多态性(SNP),其中9个位于编码外显子中(5个同义突变和4个非同义突变),20个位于内含子区域,5个位于3'-UTR。其中,9个是新的SNP,包括3个非同义SNP,即SNH313003(817733G>C;K49N)、SNH313020(848661C>A;L420M)和SNH313029(849577T>C;L577P),其次要等位基因频率分别为0.005、0.045和0.020。我们还确认了先前报道的一个非同义SNP rs1057868(A503V)以及5个同义SNP(G5G、T29T、P129P、S485S和S572S),它们的等位基因频率与先前报道的相似。在结构上,这些多态性发生在不同区域:SNH313003(K49N)位于氨基末端尾巴,SNH313020(L420M)位于连接结构域,SNH313029(L577P)位于NADPH结合结构域,rs1057868(A503V)位于FAD结合结构域。