Please use this identifier to cite or link to this item: https://doi.org/10.1097/00008571-199808000-00003
Title: Detection of mutations and polymorphism of N-acetyltransferase 1 gene in Indian, Malay and Chinese populations
Authors: Zhao, B. 
Lee, E.J.D.
Yeoh, P.N.
Gong, N.H.
Keywords: Chinese
Indians
Malays
N-acetyltransferase-1
Polymorphism
Issue Date: 1998
Citation: Zhao, B., Lee, E.J.D., Yeoh, P.N., Gong, N.H. (1998). Detection of mutations and polymorphism of N-acetyltransferase 1 gene in Indian, Malay and Chinese populations. Pharmacogenetics 8 (4) : 299-304. ScholarBank@NUS Repository. https://doi.org/10.1097/00008571-199808000-00003
Abstract: The xenobiotic metabolizing enzymes N-acetyltransferases (NATs) are important for the biotransformation and/or bioactivation of drugs and carcinogens. NATs are coded for in humans by two distinct genes, designated NAT1 and NAT2. NAT1, which was originally thought to be monomorphic, was recently reported to exhibit variation in human populations. Recent studies suggested that a genetic polymorphism of NAT1 may be associated with colorectal cancer risk. The distributions of NAT1 allele and genotype frequencies in unrelated individuals among Indian (n = 140), Malay (n = 122) and Chinese (n = 181) populations in Singapore were characterized by polymerase chain reaction-restriction fragment length polymorphism and allele-specific-polymerase chain reaction. The allelic frequencies of NAT1*3, NAT1*4, NAT1*10 and NAT1*11 among Indians were 0.3, 0.5, 0.17 and 0.27 and 0.02, respectively. The corresponding NAT1 allelic frequencies in Malays were 0.29, 0,30, 0.33 and 0.02, respectively, and were similar to those in Chinese in the region. The allelic frequencies of NAT1*3, NAT1*4, NAT1*10 and NAT1*11 among Chinese were 0.33, 0.35, 0.30 and 0.02, respectively. These findings are of importance for the determination of cancer risk in these populations. In addition, nucleotide changes at positions 350-351 (GG to CC) and 497-449 (GGG to CCC) of the NAT1 gene were not found in the alleles of the populations studied.
Source Title: Pharmacogenetics
URI: http://scholarbank.nus.edu.sg/handle/10635/116289
ISSN: 0960314X
DOI: 10.1097/00008571-199808000-00003
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