Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression

GIP plays an important regulatory role in glucose and lipid metabolism. As the specific receptor, GIPR is involved in this physiological process. To assess the roles of GIPR in teleost, the GIPR gene was cloned from grass carp. The ORF of cloned GIPR gene was 1560 bp, encoding 519 amino acids. The g...

Full description

Saved in:
Bibliographic Details
Main Authors: Guokun Yang, Xiaomin Liang, Yanle Jiang, Chengquan Li, Yanmin Zhang, Xindang Zhang, Xulu Chang, Yawei Shen, Xiaolin Meng
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Aquaculture Nutrition
Online Access:http://dx.doi.org/10.1155/2022/4330251
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850229234528681984
author Guokun Yang
Xiaomin Liang
Yanle Jiang
Chengquan Li
Yanmin Zhang
Xindang Zhang
Xulu Chang
Yawei Shen
Xiaolin Meng
author_facet Guokun Yang
Xiaomin Liang
Yanle Jiang
Chengquan Li
Yanmin Zhang
Xindang Zhang
Xulu Chang
Yawei Shen
Xiaolin Meng
author_sort Guokun Yang
collection DOAJ
description GIP plays an important regulatory role in glucose and lipid metabolism. As the specific receptor, GIPR is involved in this physiological process. To assess the roles of GIPR in teleost, the GIPR gene was cloned from grass carp. The ORF of cloned GIPR gene was 1560 bp, encoding 519 amino acids. The grass carp GIPR was the G-protein-coupled receptor which contains seven predicted transmembrane domains. In addition, two predicted glycosylation sites were contained in the grass carp GIPR. The grass carp GIPR expression is in multiple tissues and is highly expressed in the kidney, brain regions, and visceral fat tissue. In the OGTT experiment, the GIPR expression is markedly decreased in the kidney, visceral fat, and brain by treatment with glucose for 1 and 3 h. In the fast and refeeding experiment, the GIPR expression in the kidney and visceral fat tissue was significantly induced in the fast groups. In addition, the GIPR expression levels were markedly decreased in the refeeding groups. In the present study, the visceral fat accumulation of grass carp was induced by overfed. The GIPR expression was significantly decreased in the brain, kidney, and visceral fat tissue of overfed grass carp. In primary hepatocytes, the GIPR expression was promoted by treatment with oleic acid and insulin. The GIPR mRNA levels were significantly reduced by treatment with glucose and glucagon in the grass carp primary hepatocytes. To our knowledge, this is the first time the biological role of GIPR is unveiled in teleost.
format Article
id doaj-art-27df498c40684af0aaeff240854f04cf
institution OA Journals
issn 1365-2095
language English
publishDate 2022-01-01
publisher Wiley
record_format Article
series Aquaculture Nutrition
spelling doaj-art-27df498c40684af0aaeff240854f04cf2025-08-20T02:04:18ZengWileyAquaculture Nutrition1365-20952022-01-01202210.1155/2022/4330251Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its ExpressionGuokun Yang0Xiaomin Liang1Yanle Jiang2Chengquan Li3Yanmin Zhang4Xindang Zhang5Xulu Chang6Yawei Shen7Xiaolin Meng8College of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesCollege of FisheriesGIP plays an important regulatory role in glucose and lipid metabolism. As the specific receptor, GIPR is involved in this physiological process. To assess the roles of GIPR in teleost, the GIPR gene was cloned from grass carp. The ORF of cloned GIPR gene was 1560 bp, encoding 519 amino acids. The grass carp GIPR was the G-protein-coupled receptor which contains seven predicted transmembrane domains. In addition, two predicted glycosylation sites were contained in the grass carp GIPR. The grass carp GIPR expression is in multiple tissues and is highly expressed in the kidney, brain regions, and visceral fat tissue. In the OGTT experiment, the GIPR expression is markedly decreased in the kidney, visceral fat, and brain by treatment with glucose for 1 and 3 h. In the fast and refeeding experiment, the GIPR expression in the kidney and visceral fat tissue was significantly induced in the fast groups. In addition, the GIPR expression levels were markedly decreased in the refeeding groups. In the present study, the visceral fat accumulation of grass carp was induced by overfed. The GIPR expression was significantly decreased in the brain, kidney, and visceral fat tissue of overfed grass carp. In primary hepatocytes, the GIPR expression was promoted by treatment with oleic acid and insulin. The GIPR mRNA levels were significantly reduced by treatment with glucose and glucagon in the grass carp primary hepatocytes. To our knowledge, this is the first time the biological role of GIPR is unveiled in teleost.http://dx.doi.org/10.1155/2022/4330251
spellingShingle Guokun Yang
Xiaomin Liang
Yanle Jiang
Chengquan Li
Yanmin Zhang
Xindang Zhang
Xulu Chang
Yawei Shen
Xiaolin Meng
Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
Aquaculture Nutrition
title Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
title_full Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
title_fullStr Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
title_full_unstemmed Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
title_short Molecular Characterization of Grass Carp GIPR and Effect of Nutrition States, Insulin, and Glucagon on Its Expression
title_sort molecular characterization of grass carp gipr and effect of nutrition states insulin and glucagon on its expression
url http://dx.doi.org/10.1155/2022/4330251
work_keys_str_mv AT guokunyang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT xiaominliang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT yanlejiang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT chengquanli molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT yanminzhang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT xindangzhang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT xuluchang molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT yaweishen molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression
AT xiaolinmeng molecularcharacterizationofgrasscarpgiprandeffectofnutritionstatesinsulinandglucagononitsexpression