The genomic clones of human aryl hydrocarbon receptor (Ahr) and Ahr nu
clear translocator (Arnt) were isolated, and the structures of exon-in
tron junctions of these genes were partially determined. Based on the
sequence information, a quantitative RT-PCR analysis was developed, an
d the expression of these genes was studied in various human tissues.
mRNAs for Ahr and Arnt were widely expressed in human tissues and abun
dantly in lung. Individual difference in expression levels of Ahr and
Arnt mRNA was observed in liver, lung and blood. In order to examine w
hether expression levels of Ahr and Arnt were associated with those of
CYP1A1, we studied the expression of these mRNAs in blood among 20 he
althy subjects, taking account of individuals' cigarette smoking habit
s. We found that the expression levels of CYP1A1 appeared to associate
with those of Ahr and Arnt mRNAs (P < 0.06), and also that the expres
sion of Ahr and Arnt was influenced by cigarette smoking. The expressi
on of human Ahr and Arnt is reported here for the first time, providin
g a quantitative RT-PCR analysis as a useful tool for further studies.