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 catal
yse N-acetylation of arylamine carcinogens, such as benzidine and othe
r 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 encodin
g 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 delet
ions have been associated with bladder cancer [Knowles, Shaw and Proct
or (1993) Oncogene 8, 1357-1364].