Chromosome mapping of the genes for murine arylamine N-acetyltransferases (NATs), enzymes involved in the metabolism of carcinogens:: identification of a novel upstream noncoding exon for murine Nat2

被引:26
作者
Fakis, G
Boukouvala, S
Buckle, V
Payton, M
Denning, C
Sim, E
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] Univ Oxford, Inst Mol Med, Oxford OX1 3QT, England
[3] Univ Edinburgh, Ctr Genome Res, Edinburgh, Midlothian, Scotland
来源
CYTOGENETICS AND CELL GENETICS | 2000年 / 90卷 / 1-2期
关键词
D O I
10.1159/000015648
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Arylamine N-acetyltransferases (NATs) catalyse acetylation reactions which can result in either detoxification or activation of arylamine carcinogens. The human NAT loci (NAT1, NAT2, and a pseudogene, NATP) have been mapped to human chromosome 8p22, a region frequently deleted in rumours. There are three functional genes in mice (Natl, Nat2, and Nat3) encoding for three NAT isoenzymes. Different alleles at the Nat2 locus are responsible for the acetylation polymorphism identified in different mouse strains. We show that Nat3 is close to Nat1 and Nat2 by screening of a P1 artificial chromosome (PAC) library and provide cytogenetic evidence for co-localisation of the three genes in chromosome region 8 B3.1-B3.3. The Nat region of mouse and human is homologous. We also provide sequence information and a restriction map in the vicinity of Nat1 and Nat2 and describe a noncoding exon located 6 kb upstream of the Nat2 coding region. Copyright (C) 2000 S. Karger AG.
引用
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页码:134 / 138
页数:5
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