251. Molecular cloning of a proglucagon in a cyprinid fish (Schizothorax prenanti): mRNA tissue distribution and quantification during periprandial changes and fasting
- Author
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Defang Chen, Xin Zhang, Hu Chen, Jin Hao, Tao Wang, Yundi Gao, Dengyue Yuan, Fangjun Lin, Ju Liu, Hongwei Wu, and Zhiqiong Li
- Subjects
Cloning ,medicine.medical_specialty ,Vertebrate ,Aquatic Science ,Proglucagon ,Biology ,biology.organism_classification ,Glucagon ,Energy homeostasis ,Schizothorax prenanti ,Cell biology ,Oxyntomodulin ,chemistry.chemical_compound ,Endocrinology ,chemistry ,Internal medicine ,Complementary DNA ,biology.animal ,medicine - Abstract
Proglucagon is the precursor for several peptides: glucagon, glicentin, oxyntomodulin and at least one glucagon-like peptide. Previous reports indicated that proglucagon-derived peptides are important in regulating feeding and energy homeostasis in both mammals and fish. In the present study, a 504 bp cDNA fragment encoding a highly conserved proglucagon in a cyprinid fish ( Schizothorax prenanti ) was amplified by homologous cloning. Tissue expression profiles of proglucagon showed that S. prenanti proglucagon had a broad tissue distribution, but was expressed primarily in the intestine and brain. Proglucagon mRNA levels significantly increased after feeding in the hypothalamus and intestine, while levels were dramatically reduced during a week of food deprivation and increased upon refeeding. Proglucagon mRNA expression changes in the hypothalamus and intestine responded to the altered feeding status and suggest that proglucagon is involved in the regulation of feeding and energy in S. prenanti . Statement of relevance In the present study, we deal with the molecular, distribution expressions and mRNA quantification during periprandial, fasting and refeeding in lower vertebrate Ya-fish ( S. prenanti ). S. prenanti is an endemic cold temperate fish in the southwest of China valuable in both aquaculture and research. However, slow growth rate has been recognized as a major problem in S. prenanti farming, increasing the final production cost. Studies concerning the expression of genes related to feeding and growth regulation have been conducted for this species in our laboratory. Recently, a growing number of homologues of mammalian appetite-regulating peptides and their receptors have been characterized in fish. Proglucagon is the precursor for several peptides: glucagon, glicentin, oxyntomodulin and at least one glucagon-like peptide. These peptides are derived in a tissue-specific manner via post-translational proteolytic processing. Previous reports in mammals indicated that proglucagon-derived peptides are important in regulating feeding and energy homeostasis. However, there is scarce information about their physiological roles in fish. Here, we cloned a 504 bp cDNA fragment of a single proglucagon gene, that is mainly expressed in the intestine and brain and responded to changes of feeding status. These suggest that proglucagon acts as a satiety factor involved in the regulation of food intake in S. prenanti . Our findings of this study provide a basis for future research to better understand the functions and mechanisms of actions of proglucagon and will be helpful in dealing with feeding and growth issues in fishes. We believe that something in this manuscript would be of interest to the journal's readers and hope that this paper is suitable for publication in Aquaculture (Physiology and Endocrinology: Fish).
- Published
- 2015
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