Genetic polymorphisms of glycine N-acyltransferase in Japanese individuals

Drug Metabolism and Pharmacokinetics

Volumn 24, Issue 1, 2009, Pages 114-117

  Yamamoto, Akiko ^a   Nonen, Shinpei ^a   Fukuda, Tsuyoshi ^a,b   Yamazaki, Hiroshi ^c   Azuma, Junichi ^a  

^a OSAKA UNIVERSITY   (Japan)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c SHOWA PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Glycine N acyltransferase; Japanese; Nonsynonymous; Novel SNP

Indexed keywords

ACYLTRANSFERASE; ADENINE; GENOMIC DNA; GLYCINE N ACETYLTRANSFERASE; GUANINE; THYMINE; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CAUCASIAN; CONTROLLED STUDY; ENZYME POLYMORPHISM; EXON; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC VARIABILITY; GENOTYPE; HUMAN; INTRON; JAPANESE; MALE; NORMAL HUMAN; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 67649321880     PISSN: 13474367     EISSN: 18800920     Source Type: Journal    
DOI: 10.2133/dmpk.24.114     Document Type: Article

References (14)

1. Swinney, R., Hsu, S. and Tomlinson, G.: Phase I and Phase II enzyme polymorphisms and childhood cancer. J. Investig. Med., 54: 303-320 (2006).
2. Killinberg, P. G., Davidson, E. D. and Webster, L. T.: Evidence for a medium-chain fatty acid: coenzyme A ligase (adenosine monophosphate) that activates salicylate. Mol. Pharmacol., 7: 260-268 (1971).
3. Brusilow, S. W., Valle, D. L. and Batshaw, M. L.: New pathways of nitrogen excretion in inborn errors of urea synthesis. Lancet, 2: 452-454 (1979).
4. Gatley, S. J. and Sherratt, H. S. A.: The synthesis of hippurate from benzoate and glycine by rat liver mitochondria: submitochondrial localization and kinetics. Biochem. J., 166: 39-47 (1977).
5. Vessey, D. A. and Hu, J.: Isolation from bovine liver mitochondria and characterization of three distinct carboxylic acid: CoA ligases with activity toward xenobiotics. J. Biochem. Toxicol., 10: 329-337 (1995).
6. Mawal, Y., Paradis, K. and Qureshi, I. A.: Developmental profile of mitochondrial glycine N-acyltransferase in human liver. J. Pediatr., 130: 1003-1007 (1997).
7. Webster, L. T. Jr., Siddiqui, U. A., Lucas, S. V., Strong, J. M. and Mieyal, J. J.: Identification of separate acyl-CoA: glycine and acyl-CoA: L-glutamine N-acyltransferase activities in mitochondrial fractions from liver of Rhesus monkey and man. J. Biol. Chem., 251: 3352-3358 (1976).
8. Kelley, M. and Vessey, D. A.: Characterization of the acyl-CoA: amino acid N-acyltransferases form primate liver mitochondria. J. Biochem. Toxicol., 9: 153-158 (1994).
9. Tanaka, K. and Isselbacher, K. J.: The isolation and identification of N-isovalerylglycine from urine of patients with isovaleric acidemia. J. Biol. Chem., 242: 2966-2972 (1967).
10. Hutt, A. J. and Caldwell, J.: Amino acid conjugation. In Mulder, G. J. (ed.): Conjugation Reactions in Drug Metabolism, London, Taylor and Francis, 1990, pp. 273-305.
11. Tremblay, G. C. and Qureshi, I. A.: The biochemistry and toxicology of benzoic acid metabolism and its relationship to the elimination of waste nitrogen. Pharmacol. Ther., 60: 63-90 (1993).
12. Levy, G.: Pharmacokinetics of salicylate elimination in man. J. Pharm. Sci., 54: 959-967 (1965).
13. Inoue, K., Yamazaki, H., Imiya, K., Akasaka, S., Guengerich, F. P. and Shimada, T.: Relationship between CYP2C9 and 2C19 genotypes and tolbutamide methyl hydroxylation and S-mephenytoin 4′-hydroxylation activities in livers of Japanese and Caucasian populations. Pharmacogenetics, 7: 103-113 (1997).
14. Yamaori, S., Yamazaki, H., Iwano, S., Kiyotani, K., Matsumura, K., Saito, T., Parkinson, A., Nakagawa, K. and Kamataki, T.: Ethnic differences between Japanese and Caucasians in the expression levels of mRNAs for CYP3A4, CYP3A5 and CYP3A7: lack of co-regulation of the expression of CYP3A in Japanese livers. Xenobiotica, 35: 69-83 (2005).