CYP2D44 polymorphisms in cynomolgus and rhesus macaques

被引:9
作者
Uno, Yasuhiro [1 ]
Uehara, Shotaro [1 ,2 ]
Kohara, Sakae [1 ]
Osada, Naoki [3 ,4 ]
Murayama, Norie [2 ]
Yamazaki, Hiroshi [2 ]
机构
[1] Shin Nippon Biomed Labs Ltd, Pharmacokinet & Bioanal Ctr, Wakayama 6420017, Japan
[2] Showa Pharmaceut Univ, Lab Drug Metab & Pharmacokinet, Machida, Tokyo, Japan
[3] Natl Inst Genet, Dept Populat Genet, Mishima, Shizuoka 411, Japan
[4] Grad Univ Adv Studies SOKENDAI, Dept Genet, Mishima, Shizuoka, Japan
关键词
Cytochrome P450; Genetic polymorphism; Metabolic activity; Monkey; GENETIC-VARIANTS; DRUG-METABOLISM; LIVER;
D O I
10.1007/s11033-015-3863-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macaques, including cynomolgus and rhesus macaques, are important animal species used in drug metabolism studies. CYP2D44 is expressed in cynomolgus macaque liver and encodes a functional drug metabolizing enzyme, metabolizing typical human CYP2D substrates such as bufuralol and dextromethorphan. CYP2D44 is highly homologous to human CYP2D6 that is known to be polymorphic with a large inter-individual variation in metabolic activities, however, genetic polymorphisms have not been investigated in macaque CYP2D44. In the present study, screening of 78 cynomolgus and 40 rhesus macaques found a total of 67 variants, including 64 non-synonymous variants, 1 nonsense mutation, and 2 frameshift mutations, and 1 gene conversion, of which 14, 19, and 15 variants were unique to Indochinese cynomolgus macaques, Indonesian cynomolgus macaques, and Chinese rhesus macaques, respectively. Eleven of the 64 non-synonymous variants were located in substrate recognition sites, the regions important for protein function. By site-directed mutagenesis and metabolic assays, S175N, V185L, A235G, R242G, R245K, and N337D showed substantially decreased activity in bufuralol 1'-hydroxylation as compared with wild-type proteins. Moreover, two null alleles (c.128T > del and c.664G > T) were found in Indonesian cynomolgus macaques, but not in Indochinese cynomolgus macaques or Chinese rhesus macaques. These results suggest that genetic polymorphisms might account for the variability of CYP2D44-dependent metabolism in macaques.
引用
收藏
页码:1149 / 1155
页数:7
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