| First Author | Danielson PB | Year | 2001 |
| Journal | J Biol Chem | Volume | 276 |
| Issue | 25 | Pages | 22114-9 |
| PubMed ID | 11290742 | Mgi Jnum | J:70123 |
| Mgi Id | MGI:2136478 | Doi | 10.1074/jbc.M011741200 |
| Citation | Danielson PB, et al. (2001) Sturgeon orphanin, a molecular 'fossil' that bridges the gap between the opioids and orphanin FQ/nociceptin. J Biol Chem 276(25):22114-9 |
| abstractText | The elucidation of the cDNA sequence for sturgeon proorphanin provides a unique window for interpreting the evolutionary history of the opioid/orphanin gene family. The molecular 'fossil' status of this precursor can be seen in several ancestral sequence characteristics that point to its origin as a duplication of either a prodynorphin- or proenkephalin-like gene. The sturgeon proorphanin cDNA encodes a precursor protein of 194 residues, and the orphanin heptadecapeptide itself binds not only the opioid receptor-like 1 (ORL1) receptor but also the classical (mu, kappa, and delta) opioid receptors with near equal affinity. Allowing for this broad receptor specificity are several amino acid substitutions at key positions in the heptadecapeptide sequence, relative to its mammalian orthologs, that have been linked by amino acid scans and site-directed mutagenic studies to the exclusion of mammalian orphanin FQ/nociceptin from classic opioid ligands (i.e. F1Y and L14W). The unique receptor binding profile of sturgeon orphanin not only provides insight into the evolutionary history of the opioid and opioid-related peptides but also provides an ideal context in which to investigate the underlying mechanisms by which novel and often divergent physiological functions arise in receptor-ligand systems. |
