Viral infection upregulates myostatin promoter activity in orange-spotted grouper (Epinephelus coioides)

PLoS One. 2017 Oct 16;12(10):e0186506. doi: 10.1371/journal.pone.0186506. eCollection 2017.

Abstract

Myostatin is a negative regulator of myogenesis and has been suggested to be an important factor in the development of muscle wasting during viral infection. The objective of this study was to characterize the main regulatory element of the grouper myostatin promoter and to study changes in promoter activity due to viral stimulation. In vitro and in vivo experiments indicated that the E-box E6 is a positive cis-and trans-regulation motif, and an essential binding site for MyoD. In contrast, the E-box E5 is a dominant negative cis-regulatory. The characteristics of grouper myostatin promoter are similar in regulation of muscle growth to that of other species, but mainly through specific regulatory elements. According to these results, we conducted a study to investigate the effect of viral infection on myostatin promoter activity and its regulation. The nervous necrosis virus (NNV) treatment significantly induced myostatin promoter activity. The present study is the first report describing that specific myostatin motifs regulate promoter activity and response to viral infection.

MeSH terms

  • Animals
  • Base Sequence
  • Bass / genetics*
  • Bass / immunology
  • Bass / virology*
  • E-Box Elements / genetics
  • Fish Proteins / genetics*
  • Myostatin / genetics*
  • Promoter Regions, Genetic / genetics*

Substances

  • Fish Proteins
  • Myostatin

Grants and funding

This research was supported by the Ministry of Science and Technology​ ​(https://www.most.gov.tw/) (MOST 103-2321-B-006-015 and MOST​ ​103-2313-B-006-004-MY3) and the Headquarters of University Advancement at the National Cheng Kung University, which is sponsored by the Ministry of Education​ ​(https://www.edu.tw/), Taiwan.​ ​The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.