MSK1 and MSK2 are required for the mitogen- and stress-induced phosphorylation of CREB and ATF1 in fibroblasts

  • Mol Cell Biol. 2002 Apr;22(8):2871-81. doi: 10.1128/MCB.22.8.2871-2881.2002.
Giselle R Wiggin  1 ,  Ana Soloaga ,  Julia M Foster ,  Victoria Murray-Tait ,  Philip Cohen ,  J Simon C Arthur
Affiliations
  • 1. MRC Protein Phosphorylation Unit, School of Life Sciences, University of Dundee, Dundee DD1 5EH, Scotland.
Abstract

Using mouse knockouts for mitogen- and stress-activated protein kinase 1 (MSK1) and MSK2 and a double knockout of both MSK1 and MSK2, we show that these protein Kinases are required for the stress-induced phosphorylation of Transcription Factors CREB and ATF1 in primary embryonic fibroblasts. In contrast mitogen-induced phosphorylation of CREB and ATF1 is greatly reduced but not totally abolished. The mitogen- and stress-induced phosphorylation of CREB at Ser133 has been linked to the transcription of several immediate early genes, including c-Fos, junB, and egr1. The knockout of both MSK1 and MSK2 resulted in a 50% reduction in c-Fos and junB gene transcription in response to anisomycin or UV-C radiation but only a small reduction in response to tetradecanoyl phorbol acetate or epidermal growth factor in fibroblasts. The transcription of egr1 in response to both mitogenic and stress stimuli, as well as stress-induced Apoptosis, was unaffected in the MSK1/MSK2 double knockout.