Uno Yasuhiro, Jikuya Shiori, Noda Yutaro, Oguchi Asuka, Murayama Norie, Kawaguchi Hiroaki, Tsukiyama-Kohara Kyoko, Yamazaki Hiroshi
Department of Basic Veterinary Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima-city, Kagoshima 890-0065, Japan.
Department of Basic Veterinary Science, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima-city, Kagoshima 890-0065, Japan.
Comp Biochem Physiol C Toxicol Pharmacol. 2023 May;267:109579. doi: 10.1016/j.cbpc.2023.109579. Epub 2023 Feb 22.
Novel cytochrome P450 3A5 (CYP3A5) cDNA in tree shrews (which are non-rodent primate-like species) and pig CYP3A227 cDNA were identified, along with known pig CYP3A22, CYP3A29, and CYP3A46 cDNAs. All five cDNAs contained open reading frames encoding a polypeptide of 503 amino acids that shared high sequence identity (72-78 %) with human CYP3A4 and were more closely related to human CYP3As than rat CYP3As by phylogenetic analysis. CYP3A5 was the only CYP3A in the tree shrew genome, but pig CYP3A genes formed a CYP3A gene cluster in the genomic region corresponding to that of human CYP3A genes. Tree shrew CYP3A5 mRNA was predominantly expressed in liver and small intestine, among the tissues analyzed, whereas pig CYP3A227 mRNA was most abundantly expressed in jejunum, followed by liver. Metabolic assays established that tree shrew CYP3A5 and pig CYP3A proteins heterologously expressed in Escherichia coli metabolized typical human CYP3A4 substrates nifedipine and midazolam. These results suggest that novel tree shrew CYP3A5 and pig CYP3A227 were functional enzymes able to metabolize human CYP3A4 substrates in liver and small intestine, similar to human CYP3A4, although pig CYP3A227 mRNA was minimally expressed in all tissues analyzed.
在树鼩(一种非啮齿类灵长类动物样物种)中鉴定出了新型细胞色素P450 3A5(CYP3A5)cDNA,以及猪的CYP3A227 cDNA,同时还鉴定出了已知的猪CYP3A22、CYP3A29和CYP3A46 cDNA。所有这五个cDNA都包含开放阅读框,编码一个由503个氨基酸组成的多肽,该多肽与人类CYP3A4具有高度的序列同一性(72 - 78%),并且通过系统发育分析表明,与大鼠CYP3A相比,它们与人类CYP3A的关系更为密切。CYP3A5是树鼩基因组中唯一的CYP3A,但猪的CYP3A基因在与人类CYP3A基因相对应的基因组区域形成了一个CYP3A基因簇。在所分析的组织中,树鼩CYP3A5 mRNA主要在肝脏和小肠中表达,而猪CYP3A227 mRNA在空肠中表达最为丰富,其次是肝脏。代谢试验证实,在大肠杆菌中异源表达的树鼩CYP3A5和猪CYP3A蛋白能够代谢典型的人类CYP3A4底物硝苯地平和咪达唑仑。这些结果表明,新型树鼩CYP3A5和猪CYP3A227是能够在肝脏和小肠中代谢人类CYP3A4底物的功能性酶,与人类CYP3A4相似,尽管猪CYP3A227 mRNA在所有分析的组织中表达量极低。