Serum response factor is required for immediate-early gene activation yet is dispensable for proliferation of embryonic stem cells

Mol Cell Biol. 2001 Apr;21(8):2933-43. doi: 10.1128/MCB.21.8.2933-2943.2001.

Abstract

Addition of serum to mitogen-starved cells activates the cellular immediate-early gene (IEG) response. Serum response factor (SRF) contributes to such mitogen-stimulated transcriptional induction of many IEGs during the G0-G1 cell cycle transition. SRF is also believed to be essential for cell cycle progression, as impairment of SRF activity by specific antisera or antisense RNA has previously been shown to block mammalian cell proliferation. In contrast, Srf(-/-) mouse embryos grow and develop up to E6.0. Using the embryonic stem (ES) cell system, we demonstrate here that wild-type ES cells do not undergo complete cell cycle arrest upon serum withdrawal but that they can mount an efficient IEG response. This IEG response, however, is severely impaired in Srf(-/-) ES cells, providing the first genetic proof that IEG activation is dependent upon SRF. Also, Srf(-/-) ES cells display altered cellular morphology, reduced cortical actin expression, and an impaired plating efficiency on gelatin. Yet, despite these defects, the proliferation rates of Srf(-/-) ES cells are not substantially altered, demonstrating that SRF function is not required for ES cell cycle progression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Cycle
  • Colony-Forming Units Assay
  • DNA Primers / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Early Growth Response Protein 1
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Embryonic and Fetal Development / genetics
  • Genes, Immediate-Early*
  • Genes, fos
  • Immediate-Early Proteins*
  • Mice
  • Mice, Knockout
  • Microscopy, Electron, Scanning
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Serum Response Factor
  • Signal Transduction
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription Factors / genetics

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Early Growth Response Protein 1
  • Egr1 protein, mouse
  • Immediate-Early Proteins
  • Nuclear Proteins
  • Serum Response Factor
  • Transcription Factors