Orphanin FQ or nociceptin (OFQ/N), the heptadecapeptide agonist for the NOP
receptor, is derived by proteolytic processing from a precursor protein, p
reproOFQ/N, Previous studies have reported alternative splicing between exo
ns 3 and 4 of the mouse OFQ/N transcript, which, upon translation, would yi
eld precursor proteins with different C-termini, Using RT-PCR, we identifie
d similar alternative splicing of preproOFQ/N transcripts in humans and rat
s. In addition, we identified two novel human preproOFQ/N splice variants f
rom which exon 2 has been excised and which also undergo alternative splici
ng between exons 3 and 4, Exon 2 contains the translational start site for
preproOFQ/N and encodes the signal peptide sequence. In vitro translation o
f cRNAs lacking exon 2 yields shorter translation products which arise from
an alternative initiator methionine located within exon 3. The resulting p
roteins would lack a signal peptide sequence, which would likely alter thei
r cellular trafficking and processing.