The E2F1-3 transcription factors are essential for cellular proliferation

Nature. 2001 Nov 22;414(6862):457-62. doi: 10.1038/35106593.

Abstract

The retinoblastoma tumour suppressor (Rb) pathway is believed to have a critical role in the control of cellular proliferation by regulating E2F activities. E2F1, E2F2 and E2F3 belong to a subclass of E2F factors thought to act as transcriptional activators important for progression through the G1/S transition. Here we show, by taking a conditional gene targeting approach, that the combined loss of these three E2F factors severely affects E2F target expression and completely abolishes the ability of mouse embryonic fibroblasts to enter S phase, progress through mitosis and proliferate. Loss of E2F function results in an elevation of p21Cip1 protein, leading to a decrease in cyclin-dependent kinase activity and Rb phosphorylation. These findings suggest a function for this subclass of E2F transcriptional activators in a positive feedback loop, through down-modulation of p21Cip1, that leads to the inactivation of Rb-dependent repression and S phase entry. By targeting the entire subclass of E2F transcriptional activators we provide direct genetic evidence for their essential role in cell cycle progression, proliferation and development.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / physiology*
  • Cell Division / genetics
  • Cell Division / physiology*
  • Cell Line
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / genetics
  • DNA-Binding Proteins*
  • Down-Regulation
  • E2F Transcription Factors
  • E2F1 Transcription Factor
  • E2F2 Transcription Factor
  • E2F3 Transcription Factor
  • Fibroblasts / cytology
  • Gene Targeting
  • Integrases / genetics
  • Integrases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Retinoblastoma Protein / metabolism
  • S Phase / genetics
  • S Phase / physiology
  • Transcription Factors / genetics
  • Transcription Factors / physiology*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism

Substances

  • Cdkn1a protein, mouse
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • DNA-Binding Proteins
  • E2F Transcription Factors
  • E2F1 Transcription Factor
  • E2F2 Transcription Factor
  • E2F3 Transcription Factor
  • E2f1 protein, mouse
  • E2f3 protein, mouse
  • Retinoblastoma Protein
  • Transcription Factors
  • Viral Proteins
  • Cre recombinase
  • Integrases