Identification, tissue distribution and regulation of preproghrelin in the brain and gut of Schizothorax prenanti

Ghrelin is an important gastrointestinal hormone involved in the regulation of feeding in both mammals and fish. In this study, the preproghrelin cDNA sequence was cloning in the gut of Schizothorax prenanti (S. prenanti). The preproghrelin gene, encoding 103-amino acids, was strongly expressed in t...

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Veröffentlicht in:Regulatory peptides 2013-09, Vol.186 (1-3), p.18-25
Hauptverfasser: Wei, RongBin, Liu, Tao, Zhou, ChaoWei, Zhang, XingDong, Yuan, DengYue, Wang, Tao, Lin, FangJun, Chen, Hu, Wu, HongWei, Li, ZhiQiong
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container_end_page 25
container_issue 1-3
container_start_page 18
container_title Regulatory peptides
container_volume 186
creator Wei, RongBin
Liu, Tao
Zhou, ChaoWei
Zhang, XingDong
Yuan, DengYue
Wang, Tao
Lin, FangJun
Chen, Hu
Wu, HongWei
Li, ZhiQiong
description Ghrelin is an important gastrointestinal hormone involved in the regulation of feeding in both mammals and fish. In this study, the preproghrelin cDNA sequence was cloning in the gut of Schizothorax prenanti (S. prenanti). The preproghrelin gene, encoding 103-amino acids, was strongly expressed in the gut and brain using real-time quantitative RT-PCR (qPCR). The S. prenanti preproghrelin was detected in embryonic developmental stages. Further, it was detectable in unfertilized eggs, suggesting that ghrelin could be classified as maternal mRNA. An experiment was conducted to determine the expression profile of ghrelin during post-feeding and fasting status of the brain and gut. The results revealed a significant postprandial decrease in ghrelin mRNA expression in the gut 6h post-feeding (hpf) and brain (1.5 and 9hpf) compared to an unfed control group, indicating that food intake and processing affect the regulation of expression of ghrelin in S. prenanti. The constructed recombinant plasmid pMD-19T-ghrelin was transformed to Escherichia coli BL21 and induced with IPTG, and the expressed product was identified by SDS-PAGE. The prokaryotic expression vector for ghrelin was constructed successfully, and fusion protein was expressed in E. coli BL21, which laid the foundation for the further study on the function of this protein and its mechanism. Overall, our results provide evidence for a highly conserved structure and biological actions of ghrelin in S. prenanti. Further studies are required to identify the tissue specific functions of ghrelin in S. prenanti. •The ghrelin cDNA was first cloned from the gut of Schizothorax prenanti.•Ghrelin is widely expressed, notably in the gut and brain.•Our study is the first example to demonstrate the expression of ghrelin mRNA in the early embryo of Schizothorax prenanti.•Ghrelin expression fluctuated in the brain and gut during 24h post-feeding.
doi_str_mv 10.1016/j.regpep.2013.07.002
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In this study, the preproghrelin cDNA sequence was cloning in the gut of Schizothorax prenanti (S. prenanti). The preproghrelin gene, encoding 103-amino acids, was strongly expressed in the gut and brain using real-time quantitative RT-PCR (qPCR). The S. prenanti preproghrelin was detected in embryonic developmental stages. Further, it was detectable in unfertilized eggs, suggesting that ghrelin could be classified as maternal mRNA. An experiment was conducted to determine the expression profile of ghrelin during post-feeding and fasting status of the brain and gut. The results revealed a significant postprandial decrease in ghrelin mRNA expression in the gut 6h post-feeding (hpf) and brain (1.5 and 9hpf) compared to an unfed control group, indicating that food intake and processing affect the regulation of expression of ghrelin in S. prenanti. The constructed recombinant plasmid pMD-19T-ghrelin was transformed to Escherichia coli BL21 and induced with IPTG, and the expressed product was identified by SDS-PAGE. The prokaryotic expression vector for ghrelin was constructed successfully, and fusion protein was expressed in E. coli BL21, which laid the foundation for the further study on the function of this protein and its mechanism. Overall, our results provide evidence for a highly conserved structure and biological actions of ghrelin in S. prenanti. 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The constructed recombinant plasmid pMD-19T-ghrelin was transformed to Escherichia coli BL21 and induced with IPTG, and the expressed product was identified by SDS-PAGE. The prokaryotic expression vector for ghrelin was constructed successfully, and fusion protein was expressed in E. coli BL21, which laid the foundation for the further study on the function of this protein and its mechanism. Overall, our results provide evidence for a highly conserved structure and biological actions of ghrelin in S. prenanti. 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In this study, the preproghrelin cDNA sequence was cloning in the gut of Schizothorax prenanti (S. prenanti). The preproghrelin gene, encoding 103-amino acids, was strongly expressed in the gut and brain using real-time quantitative RT-PCR (qPCR). The S. prenanti preproghrelin was detected in embryonic developmental stages. Further, it was detectable in unfertilized eggs, suggesting that ghrelin could be classified as maternal mRNA. An experiment was conducted to determine the expression profile of ghrelin during post-feeding and fasting status of the brain and gut. The results revealed a significant postprandial decrease in ghrelin mRNA expression in the gut 6h post-feeding (hpf) and brain (1.5 and 9hpf) compared to an unfed control group, indicating that food intake and processing affect the regulation of expression of ghrelin in S. prenanti. The constructed recombinant plasmid pMD-19T-ghrelin was transformed to Escherichia coli BL21 and induced with IPTG, and the expressed product was identified by SDS-PAGE. The prokaryotic expression vector for ghrelin was constructed successfully, and fusion protein was expressed in E. coli BL21, which laid the foundation for the further study on the function of this protein and its mechanism. Overall, our results provide evidence for a highly conserved structure and biological actions of ghrelin in S. prenanti. Further studies are required to identify the tissue specific functions of ghrelin in S. prenanti. •The ghrelin cDNA was first cloned from the gut of Schizothorax prenanti.•Ghrelin is widely expressed, notably in the gut and brain.•Our study is the first example to demonstrate the expression of ghrelin mRNA in the early embryo of Schizothorax prenanti.•Ghrelin expression fluctuated in the brain and gut during 24h post-feeding.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23850798</pmid><doi>10.1016/j.regpep.2013.07.002</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Amino Acid Sequence
Animals
Appetite
Base Sequence
Brain - metabolism
Cloning, Molecular
Conserved Sequence
Cyprinidae - genetics
Cyprinidae - metabolism
Escherichia coli
Fish Proteins - chemistry
Fish Proteins - genetics
Fish Proteins - metabolism
Food intake
Gastrointestinal Tract - metabolism
Gene Expression Regulation, Developmental
Ghrelin
Ghrelin - chemistry
Ghrelin - genetics
Ghrelin - metabolism
Molecular Sequence Data
Organ Specificity
Phylogeny
Postprandial Period
Prokaryotic expression
Protein Precursors - chemistry
Protein Precursors - genetics
Protein Precursors - metabolism
Schizothorax
Schizothorax prenanti
Sequence Analysis, DNA
title Identification, tissue distribution and regulation of preproghrelin in the brain and gut of Schizothorax prenanti
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