MAPPING AAC1, AAC2 AND AACP, THE GENES FOR ARYLAMINE N-ACETYLTRANSFERASES, CARCINOGEN METABOLIZING ENZYMES ON HUMAN-CHROMOSOME 8P22, A REGION FREQUENTLY DELETED IN TUMORS
N. Matas et al., MAPPING AAC1, AAC2 AND AACP, THE GENES FOR ARYLAMINE N-ACETYLTRANSFERASES, CARCINOGEN METABOLIZING ENZYMES ON HUMAN-CHROMOSOME 8P22, A REGION FREQUENTLY DELETED IN TUMORS, Cytogenetics and cell genetics, 77(3-4), 1997, pp. 290-295
Arylamine N-acetyltransferases (NATs) are encoded at two loci on 8p22,
a region subject to deletions in bladder tumours. The two functional
genes (AAC1 and AAC2 alias NAT1 and NAT2) without introns in the codin
g region, encode enzymes which metabolise carcinogens, including bladd
er carcinogens. They are both multi-allelic and certain alleles have b
een implicated as susceptibility factors in bladder cancer. There is a
third N-acetyltransferase gene, a pseudogene, AACP alias NATP, which
we show is also located on chromosome 8 at the p22 region. We have map
ped a series of YAC clones (ICI and CEPH) containing the NAT genes and
the markers D8S21, an RFLP marker, and D8S261, a microsatellite marke
r. We show that D8S21 is a portion of the coding region of AAC2. The o
rder of genes in this region, covering some 2 Mb, is TEG D8S261-AAC1-A
ACP-AAC2 (D8S21)-CEN. The restriction map also illustrates that there
are likely to be other expressed genes in the region through the ident
ification of CpG islands.