Steroid receptor coactivator-1 (SRC-1) family members interact with steroid
receptors, including estrogen receptor alpha (ER alpha) and progesterone r
eceptor (PR), to enhance ligand-dependent transcription. However, the expre
ssion of ER alpha and SRC-1 was found to be segregated in distinct subsets
of cells within the epithelium of the estrogen-responsive rat mammary gland
. This finding was in contrast to the finding for the stroma, where signifi
cant numbers of cells coexpressed ER alpha and SRC-1. Treatment of animals
with estrogen induced PR expression in the ER alpha-expressing mammary epit
helial cells in the absence of detectable SRC-1 and did not affect the segr
egated pattern of SRC-1 and ER alpha expression. PR was neither expressed n
or induced by estrogen treatment in stroma, despite the coexpression of ER
alpha and SRC-1, These results suggest that SRC-1 is not necessary for ER a
lpha-mediated induction of PR in mammary epithelial cells and is also not s
ufficient, for PR induction in stromal cells expressing both ER alpha and S
RC-1. Furthermore, the expression of SRC-1 in a subpopulation of mammary ep
ithelial cells distinct from those expressing ER alpha or PR raises the pos
sibility that SRC-1 has cell type-specific functions other than simply to a
ct as coactivator for ER alpha or PR in the mammary epithelium.