Chromosomal localization of human genes for arylamine N-acetyltransferase

Author:

Hickman D1,Risch A1,Buckle V2,Spurr N K3,Jeremiah S J4,McCarthy A2,Sim E1

Affiliation:

1. Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OXI 3QT, U.K.

2. Institute of Molecular Medicine, John Radcliffe Hospital, Oxford OX3 9DU, U.K.

3. ICRF Clare Hall Laboratories, Blanche Lane, Potters Bar, Herts. EN6 3LD, U.K.

4. MRC Human Biochemical Genetics Unit (UCL), The Galton Laboratory, Wolfson House, 4 Stephenson Way, London NW1 2HE, U.K.

Abstract

Arylamine N-acetyltransferase is encoded at two loci, AAC-1 and AAC-2, on human chromosome 8. The products of the two loci are able to catalyse N-acetylation of arylamine carcinogens, such as benzidine and other xenobiotics. AAC-2 is polymorphic and individuals carrying the slow-acetylator phenotype are more susceptible to benzidine-induced bladder cancer. We have identified yeast artificial chromosome clones encoding AAC-1 and AAC-2 and have used the cloned DNAs as fluorescent probes for in situ hybridization. The hybridization patterns allow assignment of AAC-1 and AAC-2 to chromosome 8p21.3-23.1, a region in which deletions have been associated with bladder cancer [Knowles, Shaw and Proctor (1993) Oncogene 8, 1357-1364].

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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