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J. Biol. Chem., Vol. 263, Issue 18, 9001-9006, 06, 1988
NE Cooke, J Ray, JG Emery and SA Liebhaber
We have sought direct evidence for the in vivo expression of the human
growth hormone-variant (hGH-V) gene by screening a placental cDNA library
with a hGH-V-specific oligonucleotide. Nine independent hGH-V cDNA clones
were isolated and analyzed, and three distinct species were detected. Five
of these hGH-V cDNAs represent mRNAs spliced and processed in a pattern
analogous to that of the highly homologous human growth hormone and human
chorionic somatomammotropin gene transcripts. Each of the remaining four
hGH-V cDNAs contains an additional segment of 253 nucleotides corresponding
in position and sequence to the fourth intron of the hGH-V gene. In
addition, one of the mRNAs in this second group uses an alternative
downstream polyadenylation site. The alternatively spliced hGH-V mRNA,
which we refer to as hGH-V2 mRNA, constitutes approximately 30% of the
hGH-V transcripts both in the human term placenta and in a stable mouse
fibroblast line expressing the transfected hGH-V gene. The placental
expression of the hGH-V gene is specific to villous tissue. The hGH-V2 mRNA
is predicted to encode a protein which substitutes the 65 carboxyl-terminal
amino acids of hGH-V with a new 104-residue carboxyl terminus resulting in
significant divergence in their relative physical properties. The
alternative splicing of the hGH-V transcripts to hGH-V and hGH-V2 mRNAs
expands the potential complexity of the hGH-V gene's role in normal
placental function.
Two distinct species of human growth hormone-variant mRNA in the human placenta predict the expression of novel growth hormone proteins
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
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