Literature DB >> 17362948

Identification of a ghrelin-like peptide in two species of shark, Sphyrna lewini and Carcharhinus melanopterus.

Akatsuki Kawakoshi1, Hiroyuki Kaiya, Larry G Riley, Tetsuya Hirano, E Gordon Grau, Mikiya Miyazato, Hiroshi Hosoda, Kenji Kangawa.   

Abstract

In this study, we identified a ghrelin-like peptide (ghrelin-LP) in two elasmobranchs. The peptide, isoforms and cDNA encoding its precursor were isolated from the stomach of two sharks, the hammerhead (HH) shark (Sphyrna lewini) and the black-tip reef (BTR) shark (Carcharhinus melanopterus). The ghrelin-LP isolated from each shark was found to be 25 amino acids in length and exhibit high sequence homology with each other; only three amino acids were different. As has been shown in tetrapod and teleost fish ghrelins, shark ghrelin-LPs possess two forms that are distinguished by having the third serine residue (Ser) acylated by either octanoic or decanoic acid. The N-terminal four residues (GVSF), known as the active core of ghrelin, are not identical to those of other species (GSSF). Nevertheless, shark ghrelin-LP elevated Ca(2+) levels in CHO cell line expressing the growth hormone secretagogue receptor (GHS-R). Unlike teleosts ghrelin's, shark ghrelin-LPs are not amidated at the C-terminus. Messenger RNA of ghrelin-LP in the HH shark was predominantly expressed in the stomach as seen in other species, followed by the brain, intestine, gill, heart and liver. The nucleotide sequence of the ghrelin-LP gene in the HH shark was characterized to compare organization of the ghrelin gene with those in other species. The size of the HH ghrelin-LP gene was 8541 bp, two to ten times larger than that of other species studied to date. The HH ghrelin-LP gene is composed of five exons and four introns, which is the same as ghrelin genes in mammals, chicken and rainbow trout. In conclusion, the shark ghrelin-LPs identified in this study exhibit many characteristics for ghrelin in terms of peptide modifications, GHS-R activation, tissue distribution, and gene organization; however, it is necessary to further clarify their biological properties such as growth hormone-releasing or orexigenic activity before designating these peptides as ghrelin.

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Year:  2007        PMID: 17362948     DOI: 10.1016/j.ygcen.2006.10.012

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  5 in total

1.  Effects of fasting, temperature, and photoperiod on preproghrelin mRNA expression in Chinese perch.

Authors:  Yi Song; Cheng Zhao; Xu-Fang Liang; Shan He; Changxu Tian; Xiaoyan Cheng; Xiaochen Yuan; Liyuan Lv; Wenjie Guo; Min Xue; Ya-Xiong Tao
Journal:  Fish Physiol Biochem       Date:  2017-03-20       Impact factor: 2.794

2.  Ghrelin cells in the gastrointestinal tract.

Authors:  Ichiro Sakata; Takafumi Sakai
Journal:  Int J Pept       Date:  2010-03-14

Review 3.  Different forms of ghrelin exhibit distinct biological roles in tilapia.

Authors:  Larry G Riley
Journal:  Front Endocrinol (Lausanne)       Date:  2013-09-03       Impact factor: 5.555

4.  Determination of Ghrelin Structure in the Barfin Flounder (Verasper moseri) and Involvement of Ingested Fatty Acids in Ghrelin Acylation.

Authors:  Hiroyuki Kaiya; Tadashi Andoh; Takashi Ichikawa; Noriko Amiya; Kouhei Matsuda; Kenji Kangawa; Mikiya Miyazato
Journal:  Front Endocrinol (Lausanne)       Date:  2013-09-03       Impact factor: 5.555

5.  Ghrelin-like peptide with fatty acid modification and O-glycosylation in the red stingray, Dasyatis akajei.

Authors:  Hiroyuki Kaiya; Shiho Kodama; Koutaro Ishiguro; Kouhei Matsuda; Minoru Uchiyama; Mikiya Miyazato; Kenji Kangawa
Journal:  BMC Biochem       Date:  2009-12-14       Impact factor: 4.059

  5 in total

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