Jd. Lin et al., 3 NEW MEMBERS OF THE MOUSE PROLACTIN GROWTH-HORMONE FAMILY ARE HOMOLOGOUS TO PROTEINS EXPRESSED IN THE RAT, Endocrinology, 138(12), 1997, pp. 5541-5549
A search of a mouse expressed sequence tag database for novel messenge
r RNAs (mRNAs) in the PRL/GH family has identified three clones that a
re homologous to the rat PRL-like protein A (PLP-A), PRL-like protein
B (PLP-B), and decidual/trophoblast PRL-related protein (d/tPRP). Full
-length complementary DNA clones for each of these three mouse mRNAs h
ave been sequenced. Mouse PLP-A is predicted to be synthesized as a pr
ecursor of 227 residues and secreted as a glycoprotein of 196 amino ac
ids; the secreted protein shares 78% identity with rat PLP-A. The open
reading frame for mouse PLP-B encodes a protein of 230 residues; the
putative mature glycoprotein of 201 amino acids is 66% identical to ra
t PLP-B. The third mouse complementary DNA clone encodes a precursor p
rotein of 240 residues and a secreted glycoprotein of 211 amino acids
with 64% identity to rat d/tPRP. All three mouse mRNAs are expressed s
pecifically in the placenta or decidua. The highest levels of the PLP-
A mRNA are detected on day 12, at which time expression is localized t
o a subset of trophoblast giant cells, especially those cells that lin
e maternal blood sinuses. PLP-B mRNA. levels are high on day 10 in dec
idual cells and on day 12 in spongiotrophoblasts. The mRNA similar to
rat d/tPRP is present at high levels even earlier in gestation (day 8)
and is localized to the decidual layer. The identification of PRL-rel
ated mRNAs in common between the mouse and rat indicates that the enco
ded hormones are evolutionarily conserved and, therefore, likely to pl
ay important roles in reproductive physiology.