Literature DB >> 25637673

Peroxisome proliferator-activated receptor gamma (PPARγ) in yellow catfish Pelteobagrus fulvidraco: molecular characterization, mRNA expression and transcriptional regulation by insulin in vivo and in vitro.

Jia-Lang Zheng1, Mei-Qin Zhuo2, Zhi Luo3, Ya-Xiong Pan2, Yu-Feng Song2, Chao Huang2, Qing-Ling Zhu2, Wei Hu2, Qi-Liang Chen2.   

Abstract

Peroxisome proliferator-activated receptor gamma (PPARγ) is ligand-inducible transcription factor and has important roles in lipid metabolism, cell proliferation and inflammation. In the present study, yellow catfish Pelteobagrus fulvidraco PPARγ cDNA was isolated from liver by RT-PCR and RACE, and its molecular characterization and transcriptional regulation by insulin in vivo and in vitro were determined. The generation of PPARγ1 and PPARγ2 was due to alternative promoter of PPARγ gene. PPARγ1 and PPARγ2 mRNA covered 2426 bp and 2537 bp, respectively, with an open reading frame (ORF) of 1584 bp encoding 527 amino acid residues. Yellow catfish PPARγ gene was organized in a manner similar to that of their mammalian homologs, implying a modular organization of the protein's domains. A comparison between the yellow catfish PPARγ amino acid sequence and the correspondent sequences of several other species revealed the identity of 55-76.2%. Two PPARγ transcripts (PPARγ1 and PPARγ2) mRNAs were expressed in a wide range of tissues, but the abundance of each PPARγ mRNA showed the tissue- and developmental stage-dependent expression patterns. Intraperitoneal injection of insulin in vivo significantly stimulated the mRNA expression of total PPARγ and PPARγ1, but not PPARγ2 in the liver of yellow catfish. In contrast, incubation of hepatocytes with insulin in vitro increased the mRNA levels of PPARγ1, PPARγ2 and total PPARγ. To our knowledge, for the first time, the present study provides evidence that PPARγ1 and PPARγ2 are differentially expressed with and among tissues during different developmental stages and also regulated by insulin both in vivo and in vitro, which serves to increase our understanding on PPARγ physiological function in fish.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Alternative splicing; Insulin; Molecular cloning; PPARγ; Pelteobagrus fulvidraco; Tissue expression

Mesh:

Substances:

Year:  2015        PMID: 25637673     DOI: 10.1016/j.ygcen.2014.12.020

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


  5 in total

1.  Novel insights for PI3KC3 in mediating lipid accumulation in yellow catfish Pelteobagrus fulvidraco.

Authors:  Mei-Qin Zhuo; Jun Chen; Mei-Li Wu; Wen-Biao Wang
Journal:  Fish Physiol Biochem       Date:  2022-04-07       Impact factor: 2.794

2.  Structure and Functional Analysis of Promoters from Two Liver Isoforms of CPT I in Grass Carp Ctenopharyngodon idella.

Authors:  Yi-Huan Xu; Zhi Luo; Kun Wu; Yao-Fang Fan; Wen-Jing You; Li-Han Zhang
Journal:  Int J Mol Sci       Date:  2017-11-13       Impact factor: 5.923

3.  Lipid metabolism-related gene expression pattern of Atlantic bluefin tuna (Thunnus thynnus L.) larvae fed on live prey.

Authors:  Mónica B Betancor; Aurelio Ortega; Fernando de la Gándara; Douglas R Tocher; Gabriel Mourente
Journal:  Fish Physiol Biochem       Date:  2016-11-04       Impact factor: 2.794

4.  Functional Analysis of Promoters of Genes in Lipid Metabolism and Their Transcriptional Response to STAT3 under Leptin Signals.

Authors:  Kun Wu; Xiao-Ying Tan; Yi-Huan Xu; Guang-Hui Chen; Mei-Qin Zhuo
Journal:  Genes (Basel)       Date:  2018-07-03       Impact factor: 4.096

5.  Functional Analysis of Promoters from Three Subtypes of the PI3K Family and Their Roles in the Regulation of Lipid Metabolism by Insulin in Yellow Catfish Pelteobagrus fulvidraco.

Authors:  Mei-Qin Zhuo; Zhi Luo; Yi-Huan Xu; Dan-Dan Li; Ya-Xiong Pan; Kun Wu
Journal:  Int J Mol Sci       Date:  2018-01-16       Impact factor: 5.923

  5 in total

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