Extracellular signal regulated kinase 5 (ERK5) is required for the differentiation of muscle cells

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Dragomir Dinev - , University of Würzburg (Author)
  • Bruce W M Jordan - , University of Würzburg (Author)
  • Bernd Neufeld - , University of Würzburg (Author)
  • Jiing-Dwan Lee - , Scripps Research Institute (Author)
  • D Lindemann - , Institute of Medical Microbiology and Virology (Author)
  • Ulf R Rapp - , University of Würzburg (Author)
  • Stephan Ludwig - , University of Würzburg (Author)

Abstract

Extracellular signal regulated kinase 5 (ERK5) is a novel member of the mitogen-activated protein kinase (MAPK) family with a poorly defined physiological function. Since ERK5 and its upstream activator MEK5 are abundant in skeletal muscle we examined a function of the cascade during muscle differentiation. We show that ERK5 is activated upon induction of differentiation in mouse myoblasts and that selective activation of the pathway results in promoter activation of differentiation-specific genes. Moreover, myogenic differentiation is completely blocked when ERK5 expression is inhibited by antisense RNA. Thus, we conclude that the MEK5/ERK5 MAP kinase cascade is critical for early steps of muscle cell differentiation.

Details

Original languageEnglish
Pages (from-to)829-34
Number of pages6
JournalEMBO reports
Volume2
Issue number9
Publication statusPublished - Sept 2001
Peer-reviewedYes

External IDs

PubMedCentral PMC1084032
Scopus 0034769309
ORCID /0000-0002-0320-4223/work/150884981

Keywords

Keywords

  • Animals, Blotting, Western, Cell Differentiation, Cell Line, Enzyme Activation, Genes, Dominant, Genes, Reporter, Humans, MAP Kinase Kinase 5, MAP Kinase Signaling System, Mice, Mitogen-Activated Protein Kinase 7, Mitogen-Activated Protein Kinase Kinases/metabolism, Mitogen-Activated Protein Kinases/metabolism, Muscle, Skeletal/cytology, Muscles/cytology, Oligonucleotides, Antisense/metabolism, Promoter Regions, Genetic, RNA, Messenger/metabolism, Signal Transduction, Time Factors, Transduction, Genetic, Transfection