In this report, we have investigated placental lactogens (placental la
ctogen-I, PL-I; PL-I variant, PL-Iv; PL-II) expressed by differentiate
d Rcho-1 trophoblast cells. A complementary DNA (cDNA) library to diff
erentiated Rcho-1 trophoblast cells was constructed and screened with
probes to detect PLI and PL-II. Sequence analysis of three independent
Rcho-1 PL-I cDNAs indicated that they significantly differed from the
previously reported PL-I sequence but more closely resembled a relate
d cDNA referred to as PL-I mosaic (PL-Im). Upon further analysis, Rcho
-1 PL-I/PL-Im transcripts could be detected in Rcho-1 trophoblast cell
s and normal developing placental tissue; however, the previously repo
rted PL-I transcript could not be identified from the same sources. Gi
ven these results, we reexamined the original PL-I cDNA by PCR and nuc
leotide sequence analyses. The sequence differed from the original rep
ort and was found to be identical to the Rcho-1 PL-I and PL-Im cDNA cl
ones. Thus, PL-I, Rcho-1 PL-I, and PL-Im are equivalent and should be
referred to as PL-I. The PL-I gene was localized to chromosome 17 of t
he rat genome, similar to other PRL family members. Rcho-1 PL-II cDNAs
were identical to the published PL-II sequence, PL-Iv cDNAs were isol
ated from differentiated Rcho-1 cells via an RT-PCR strategy and found
to be identical to previously isolated PL-Iv cDNAs. Rcho-1 PL-I and P
L-II cDNAs were subcloned into the pcDNA3 expression vector and recomb
inant protein produced in HRP-1 cells. Both recombinant Rcho-1 PL-I an
d PL-II proteins significantly stimulated the proliferation of lactoge
n-dependent rat Nb2 lymphoma cells and mouse mammary epithelial cells.
In summary, we show that the Rcho-1 PL-I corresponds to PL-Im and Rch
o-1 PL-IV and PL-II are identical to their previously described placen
tal counterparts. Additionally, both recombinant Rcho-1 PL-I and PL-II
proteins are biologically active.