We have isolated the cDNA encoding the cytoplasmic domain of a long fo
rm of the mouse PRL receptor (PRL-R). The mRNA for this long form PRL-
R and the three mRNAs encoding short mouse PRL-R that have been previo
usly characterized are all expressed in both the liver and ovary. The
relative amounts of these receptor forms differ between tissues, howev
er. In addition, the structure of one of the short receptor forms may
not be identical in the liver and ovary. Within the ovary, the abundan
ce and sites of synthesis of the four PRL-R mRNAs vary during pregnanc
y. Expression of the two most abundant PRL-R mRNAs increases significa
ntly at midgestation. Expression of PRL-R mRNA is detected in the corp
us luteum throughout pregnancy, while increased receptor mRNA levels a
re evident in the granulosa cells of a subset of Graafian follicles to
ward the end of pregnancy and during lactation. Some differences are a
lso observed in the expression patterns of the individual receptor for
ms. Most notably, one of the short form PRL-R mRNAs is uniquely detect
ed in atretic follicles in early to midgestation.