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CBP/p300 histone acetyl-transferase activity is important for the G1/S transition

  • Slimane Ait-Si-Ali
  • , Anna Polesskaya
  • , Stéphanie Filleur
  • , Roger Ferreira
  • , Arnaud Duquet
  • , Philippe Robin
  • , Arlette Vervish
  • , Didier Trouche
  • , Florence Cabon
  • , Annick Harel-Bellan
  • Laboratoire 'Oncogenèse
  • CNRS

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

127 Citations (Scopus)

Résumé

Transforming viral proteins such as E1A which force quiescent cells into S phase have two essential cellular target proteins, Rb and CBP/p300. Rb regulates the G1/S transition by controlling the transcription factor E2F. CBP/p300 is a transcriptional co-activator with intrinsic histone acetyl-transferase activity. This activity is regulated in a cell cycle dependent manner and shows a peak at the G1/S transition, suggesting a function for CBP/p300 in this crucial step of the cell cycle. Here, we have artificially modulated CBP/p300 levels in individual cells through microinjection of specific antibodies and expression vectors. We show that CBP/p300 is required for cell proliferation and has an essential function during the G1/S transition. Using the same microinjection system and GFP-reporter vectors, we demonstrate that CBP/p300 is essential for the activity of E2F, a transcription factor that controls the G1/S transition. In addition, our results suggest that CBP HAT activity is required both for the G1/S transition and for E2F activity. Thus CBP/p300 seems to be a versatile protein involved in opposing cellular processes, which raises the question of how its multiple activities are regulated.

langue originaleAnglais
Pages (de - à)2430-2437
Nombre de pages8
journalOncogene
Volume19
Numéro de publication20
Les DOIs
étatPublié - 11 mai 2000
Modification externeOui

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