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Cited by 494

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Autoregulatory control of E2F1 expression in response to positive and negative regulators of cell cycle progression.

Open access
Johnson, D G, Ohtani, K, Nevins, J R·1994·Genes & Development

Abstract

Both positive and negative signals govern the progression of cells from G1 into S phase, and a variety of data implicate the E2F transcription factor as a target for the action of one class of negative regulators, the Rb family of growth suppressors. We now find that the E2F1 gene, which encodes one of the components of E2F activity, is subject to autoregulatory control during progression from G0 to S phase and that this primarily reflects a negative control in G0 and early G1, a time when the majority of E2F activity exits as a complex with Rb family members. In addition, we find that deregulated expression of G1 cyclins in quiescent cells stimulates the E2F1 promoter and that this is augmented by coexpression of cyclin-dependent kinases in an E2F-dependent manner. We conclude that the E2F1 gene is a downstream target for G1 cyclin-dependent kinase activity, most likely as a consequence of phosphorylation of Rb family members, and that the autoregulation of E2F1 transcription may provide a sensitive switch for regulating the accumulation of E2F activity during the transition from G1 to S phase.

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Metadata

Authors
Johnson, D. G., Ohtani, K., & Nevins, J. R.
Venue
Genes & Development
Published
1994-07-01
Volume
8
Issue
13
Pages
1514-1525
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2137961581
Cited by
494
References
1
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Autoregulatory control of E2F1 expression in response to positive and negative regulators of cell cycle progression. https://app.cochat.ai/papers/10.1101/gad.8.13.1514
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Johnson, D. G., Ohtani, K., & Nevins, J. R. (1994). Autoregulatory control of E2F1 expression in response to positive and negative regulators of cell cycle progression. Genes & Development. https://doi.org/10.1101/gad.8.13.1514

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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