Induction of the SHARP-2 mRNA level by insulin is mediated by multiple signaling pathways

Biosci Biotechnol Biochem. 2017 Feb;81(2):256-261. doi: 10.1080/09168451.2016.1249450. Epub 2016 Oct 28.

Abstract

The rat enhancer of split- and hairy-related protein-2 (SHARP-2) is an insulin-inducible transcription factor which represses transcription of the rat phosphoenolpyruvate carboxykinase gene. In this study, a regulatory mechanism of the SHARP-2 mRNA level by insulin was analyzed. Insulin rapidly induced the level of SHARP-2 mRNA. This induction was blocked by inhibitors for phosphoinositide 3-kinase (PI 3-K), protein kinase C (PKC), and mammalian target of rapamycin (mTOR), actinomycin D, and cycloheximide. Whereas an adenovirus infection expressing a dominant negative form of atypical PKC lambda (aPKCλ) blocked the insulin-induction of the SHARP-2 mRNA level, insulin rapidly activated the mTOR. Insulin did not enhance transcriptional activity from a 3.7 kb upstream region of the rat SHARP-2 gene. Thus, we conclude that insulin induces the expression of the rat SHARP-2 gene at the transcription level via both a PI 3-K/aPKCλ- and a PI 3-K/mTOR- pathways and that protein synthesis is required for this induction.

Keywords: SHARP-2; atypical protein kinase C lambda; insulin; mammalian target of rapamycin; phosphoinositide 3-kinase.

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / biosynthesis
  • Basic Helix-Loop-Helix Transcription Factors / genetics*
  • Cell Line, Tumor
  • Homeodomain Proteins / biosynthesis
  • Homeodomain Proteins / genetics*
  • Insulin / pharmacology*
  • Isoenzymes / genetics
  • Protein Kinase C / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Signal Transduction / drug effects*
  • TOR Serine-Threonine Kinases / metabolism
  • Transcription, Genetic / drug effects

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Bhlhe40 protein, rat
  • Homeodomain Proteins
  • Insulin
  • Isoenzymes
  • RNA, Messenger
  • TOR Serine-Threonine Kinases
  • Protein Kinase C
  • protein kinase C lambda