Regulation of myostatin promoter activity by myocyte enhancer factor 2.
- Author:
Jia LI
1
;
Jie DENG
;
Junlin ZHANG
;
De CHENG
;
Huayan WANG
Author Information
1. Department of Animal Biotechnology, College of Veterinary Medicine, Northwest A&F University, Yangling 712100, Shaanxi, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Cells, Cultured;
Gene Expression Regulation;
MEF2 Transcription Factors;
Mice;
Muscle, Skeletal;
metabolism;
Myoblasts;
cytology;
Myogenic Regulatory Factors;
genetics;
physiology;
Myostatin;
genetics;
physiology;
Promoter Regions, Genetic;
Swine
- From:
Chinese Journal of Biotechnology
2012;28(8):918-926
- CountryChina
- Language:Chinese
-
Abstract:
Myostatin (Mstn) is a member of the transforming growth factor-beta superfamily that functions as a negative regulator of skeletal muscle growth and differentiation in mammals. The transcriptional regulation of Mstn is controlled by multiple genes including MEF2, which raise the importance of identifying the binding sites of MEF2 on myostatin promoter region and mechanisms underlying. In this study, we investigated the transcriptional regulation of MEF2 on porcine Mstn promoter activity in C2C12 cells. Sequence analysis of the 1 969 bp porcine Mstn promoter region revealed that it contained three potential MEF2 motifs. Using a serial deletion strategy, we tested the activity of several promoter fragments by luciferase assay. Overexpression of MEF2C, but not MEF2A increased Mstn promoter activity in all the promoter fragments with MEF2 motifs by two to six folds, in both C2C12 myoblasts and myotubes. When we transfected exogenous MEF2C, Mstn mRNA level was also upregulated in C2C12 cells, but the protein level was only significantly increased in myotubes. Thus, we propose that MEF2C could modulate and restrain myogenesis by Mstn activation and Mstn-dependent gene processing in porcine. Our research also provided potential targets and an effective molecule to regulate Mstn expression and gave a new way to explore the functional performance of Mstn.
