4.2 Article

Purification, cDNA cloning, and characterization of ghrelin in channel catfish, Ictalurus punctatus

Journal

GENERAL AND COMPARATIVE ENDOCRINOLOGY
Volume 143, Issue 3, Pages 201-210

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygcen.2005.03.012

Keywords

catfish; ghrelin; purification; cDNA cloning; GH; expression; real-time PCR

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The ghrelin peptide and cDNA encoding precursor protein were isolated from the stomach of a channel catfish, Ictalurus punctatus. Catfish ghrelin is a 22-amino acid peptide with a sequence of GSSFLSPTQKPQNRGDRKPPRV. The third serine residue has been modified by n-decanoic acid and unsaturated fatty acids; however, an octanoylated form could not be identified. The carboxyl end of the peptide possessed an amide structure. A Gly-extended, non-amidated 23-amino acid ghrelin (ghrelin-Gly) was also isolated. Real-time quantitative PCR analysis revealed high levels of gene expression in the stomach and moderate levels in the pancreas and gall bladder. Intraperitoneal (IP) injection of ghrelin increased plasma GH levels in the catfish, but the effect of ghrelin-Gly was more potent than that of amidated ghrelin. Furthermore, IP injection with both amidated ghrelin and ghrelin-Gly caused a significant increase in pituitary GH mRNA expression over a 3-h period. These results indicate that ghrelin is present in catfish and stimulates GH gene expression and GH release in channel catfish. (c) 2005 Elsevier Inc. All rights reserved.

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