Adenovirus E1A activates cyclin A gene transcription in the absence of growth factors through interaction with p107

J Virol. 1996 Apr;70(4):2637-42. doi: 10.1128/JVI.70.4.2637-2642.1996.

Abstract

Using the infection of quiescent human fibroblasts with adenovirus type 5 and various deletion mutants, we show that E1A can stimulate transcription of the cyclin A gene in the absence of exogenous growth factors. Required for this activity is conserved region 2 (CR2), while both the N-terminal part of E1A and CR1 are dispensable. This indicates that activation of cyclin A gene expression requires the binding of E1A to p107, while binding to either pRB or p300 is not involved in transcriptional activation. We demonstrate that p107 represses the cyclin A promoter through its cell cycle-regulatory E2F binding site and that 12S E1A can activate the cyclin A promoter, essentially by counteracting its repression by p107. Since Cr2 is required for cell transformation, transcriptional activation of the cyclin A gene by E1A appears to be important for its capacity to override control of cellular growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Adenoviruses, Human / metabolism*
  • Animals
  • Binding Sites
  • Cell Line
  • Cyclins / genetics*
  • Gene Expression Regulation, Viral*
  • Humans
  • Mice
  • Nuclear Proteins / metabolism*
  • Promoter Regions, Genetic
  • RNA, Messenger / metabolism
  • Retinoblastoma-Like Protein p107
  • Transcriptional Activation

Substances

  • Cyclins
  • Nuclear Proteins
  • RBL1 protein, human
  • RNA, Messenger
  • Rbl1 protein, mouse
  • Retinoblastoma-Like Protein p107