To determine whether the progesterone receptor (PR) gene is expressed
in rat corpora lutea (CL), PR messenger RNA (mRNA) and protein levels
were examined in CL of both cycling and pregnant rats using in situ hy
bridization, reverse transcription-polymerase chain reaction, and West
ern blotting analyses. During the estrous cycle, levels of luteal PR m
RNA were below the sensitivity of in situ hybridization. Although no s
ignal could be detected in luteal cells, granulosa cells of preovulato
ry follicles of the same ovary expressed PR mRNA at high levels during
the evening of proestrus. Likewise, CL of pregnant rats expressed und
etectable levels of PR mRNA, which remained unchanged throughout pregn
ancy, as determined by in situ hybridization and reverse transcription
-polymerase chain reaction. In addition, no PR protein could be detect
ed in rat CL by Western analysis, indicating that luteal expression of
the PR gene, if any, is negligible. To determine whether the lack of
PR mRNA in the rat CL is due to progesterone-induced down-regulation o
f PR mRNA or to low levels of estrogen, aminoglutethimide was used to
block the synthesis of progesterone in the presence and absence of exo
genous estrogen, and PR mRNA levels were examined in the CL as well as
the placenta. Inhibition of progesterone synthesis did increase PR mR
NA levels in the placenta, and additional estrogen treatment further i
ncreased PR mRNA levels in this tissue. In contrast, neither aminoglut
ethimide alone nor aminoglutethimide plus estrogen induced PR mRNA exp
ression in CL of the same rats. The temperature-sensitive luteal cell
line derived from the rat CL, which produces very low levels of proges
terone, also did not express PR mRNA. These results indicate that the
rat corpus luteum expresses undetectable levels of PR mRNA and protein
, which is not attributable to progesterone-induced down-regulation of
PR mRNA or to a lack of estrogen-induced up-regulation of PR mRNA in
this tissue.