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Departments of Zoology (H.Z., M.H., Y.J., A.O.L.W.) and Chemistry and Open Laboratory of Chemical Biology (K.H.S., Y.Y.), The University of Hong Kong, Hong Kong SAR, Peoples Republic of China
Address all correspondence and requests for reprints to: Anderson O. L. Wong, Department of Zoology, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, P.R. China. E-mail: olwong{at}hkucc.hku.hk.
Pituitary adenylate cyclase-activating polypeptide (PACAP) has been proposed to be the ancestral GHRH. Recently, using grass carp as a model for modern-day bony fish, we demonstrated that PACAP nerve fibers are present in close proximity to carp somatotrophs, and mammalian PACAPs can induce GH secretion in carp pituitary cells. To further examine the role of PACAP as a GH-releasing factor in fish, the structural identity of grass carp PACAP was established by molecular cloning. The newly cloned PACAP was found to be a single-copy gene and expressed in the brain but not other tissues. The mature peptides of PACAP, namely PACAP27 and PACAP38, were synthesized. As revealed by nuclear magnetic resonance spectroscopies, carp PACAP38 is composed of a flexible N terminal from His1 to Ile5, an extended central helix from Phe6 to Val26, and a short helical tail in the C terminal from Arg29 to Arg34. The C-terminal helix is located after a hinge region at Leu27 to Gly28 and is absent in the solution structures of PACAP27. The two forms of PACAPs were effective in elevating GH release and GH transcript expression in grass carp pituitary cells. These stimulatory effects occurred with parallel rises in cAMP and Ca2+ entry via voltage-sensitive Ca2+ channels in carp somatotrophs. The present study represents the first report for solution structures of nonmammalian PACAPs and provides evidence that a brain-specific isoform of PACAP in fish can stimulate GH synthesis and release at the pituitary level, presumably by activating the appropriate postreceptor signaling mechanisms.
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