Identification of novel E2F1-regulated genes by microarray

Yihong Ma1, Rhonda Croxton, Ronnie L Moorer

  • 1Program in Molecular Oncology, H. Lee Moffitt Comprehensive Cancer Center and Research Institute, University of South Florida, Tampa, 33612, USA.

Insights

The E2F1 transcription factor activates genes for cell cycle progression. This study reveals E2F1 also impacts apoptosis, signal transduction, and surprisingly, represses other genes.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Genomics

Background:

  • The E2F pathway is hypothesized to control the transition from quiescence to DNA synthesis.
  • Previous research has not rigorously tested this hypothesis on a genomic scale.

Purpose of the Study:

  • To investigate the genomic-scale effects of E2F1 on gene expression in quiescent cells.
  • To identify novel cellular functions regulated by E2F1.

Main Methods:

  • Infection of quiescent mouse fibroblasts lacking E2F1 with an adenovirus expressing E2F1.
  • Analysis of gene expression for over 6000 genes using high-density microarrays.

Main Results:

  • Microarray data support E2F1's role in regulating genes for DNA synthesis.
  • E2F1 was found to influence pathways involved in apoptosis, signal transduction, transcriptional control, and membrane biology.
  • A significant number of genes were identified as being repressed by E2F1, indicating a potential transcriptional repression role.

Conclusions:

  • E2F1 plays a key role in activating genes essential for cell cycle progression.
  • E2F1 regulates a broader range of cellular functions than previously understood.
  • E2F1 may possess a novel mechanism for repressing gene transcription.