Bd. Abbott et al., DEVELOPMENTAL EXPRESSION OF 2 MEMBERS OF A NEW CLASS OF TRANSCRIPTIONFACTORS .1. EXPRESSION OF ARYL-HYDROCARBON RECEPTOR IN THE C57BL 6N MOUSE EMBRYO/, Developmental dynamics, 204(2), 1995, pp. 133-143
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcriptio
n factor with a basic region/helix-loop-helix (bHLH) motif. AhR has be
en sequenced and the functional domains defined and there is informati
on on the formation of complexes with other peptides and interactions
with DNA, although these areas continue to be investigated, AhR mediat
es many biological effects such as developmental toxicity, including i
nduction of cleft palate and hydronephrosis, This regulatory protein i
s expressed in embryonic liver and has been immunohistochemically loca
lized in cells of human and mouse secondary palate. The expression of
AhR in embryonic tissues and its ability to disrupt development sugges
ts a significant role for this protein in development, The present stu
dy examines the pattern of AhR expression in the C57BL/6N mouse embryo
from gestation days (GD) 10-16, using in situ hybridization and immun
ohistochemical analysis. AhR mRNA was localized with S-35-RNA antisens
e riboprobe (cAh1 probe, 1.8 Kb amino terminal DNA), AhR protein was l
ocalized with purified monoclonal antibody (RPT-9) raised against the
N-terminal peptide sequence. AhR mRNA and protein were expressed in GD
10-13 neuroepithelium, and as development progressed the levels in br
ain decreased. GD 10-12 embryos also showed AhR in branchial arches, h
eart, somites, and liver, AhR protein and mRNA in heart were highest a
t GD 10-11 and decreased with age. In liver, AhR mRNA and protein leve
ls increased and nuclear localization became more pronounced with gest
ational age. In GD 14-16 embryos levels in liver and adrenal were high
est, but AhR was present in ectoderm, bone, and muscle. AhR expression
was specific for both cell type, organ/tissue, and developmental stag
e, suggesting that this novel ligand-activated transcriptional regulat
or may be important in normal embryonic development. (C) 1995 Wiley-Li
ss, Inc.