c-Myb negatively regulates Ras signaling through induction of dual phosphatase MKP-3 in NIH3T3 cells

Biochem Biophys Res Commun. 2014 Jul 25;450(2):1032-7. doi: 10.1016/j.bbrc.2014.06.103. Epub 2014 Jun 27.

Abstract

Mitogen-activated protein kinase phosphatase-3 (MKP-3) negatively regulates ERK1/2 MAPK in a feedback loop. However, little is known about the molecular mechanism by which Ras signaling induces MKP-3 expression. In the present study, we demonstrate that exogenous expression of constitutively active H-Ras increases the level of MKP-3 mRNA. A transfection study using a series of MKP-3 promoter deletion constructs revealed that the c-Myb binding site is required for Ras-induced transcriptional activation of the MKP-3 gene promoter. Furthermore, we show that c-Myb directly binds to the MKP-3 promoter, as revealed by electrophoretic mobility shift assay and chromatin immunoprecipitation. Knock-down of c-Myb expression using siRNA abrogated Ras-induced MKP-3 promoter activity. These findings propose a novel mechanism through which Ras signaling activates c-Myb-dependent transcriptional activation of the MKP-3 gene.

Keywords: ERK; H-Ras; MKP-3; NIH3T3 fibroblasts; c-Myb.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dual Specificity Phosphatase 6 / biosynthesis*
  • Dual Specificity Phosphatase 6 / genetics
  • Enzyme Induction
  • Mice
  • NIH 3T3 Cells
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins c-myb / metabolism*
  • Signal Transduction
  • Transcription, Genetic
  • Up-Regulation
  • ras Proteins / metabolism*

Substances

  • Proto-Oncogene Proteins c-myb
  • Dual Specificity Phosphatase 6
  • Dusp6 protein, mouse
  • ras Proteins