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Cited by 444

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Serum-, TPA-, and Ras-induced expression from Ap-1/Ets-driven promoters requires Raf-1 kinase.

Open access
Bruder, J T, Heidecker, G, Rapp, U R·1992·Genes & Development

Abstract

Raf-1 serine-threonine protein kinase has the hallmarks of a critical switch that connects growth factor receptor activation at the cell membrane with transcriptional events in the nucleus. We show by use of Raf-1 dominant-negative mutants that Raf-1 is required for serum-, TPA-, and Ras-induced expression from the oncogene-responsive element in the polyomavirus enhancer. The minimal region of Raf-1 that displays this dominant-negative phenotype (Raf-C4) contains a cysteine finger motif. Raf-C4 appears to function by titrating out a Raf-1-activating factor that is induced by Ras following serum or TPA treatment of NIH-3T3 cells. In addition, we show that Raf-1 and Ras cooperate in trans-activation through the oncogene-responsive element and that the cysteine-rich region is necessary for this effect.

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Metadata

Authors
Bruder, J. T., Heidecker, G., & Rapp, U. R.
Venue
Genes & Development
Published
1992-04
Volume
6
Issue
4
Pages
545-556
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2171569176
Cited by
444
References
1
Type
posted content
Language
en
Open access
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CoChat. (2026). Citation check: Serum-, TPA-, and Ras-induced expression from Ap-1/Ets-driven promoters requires Raf-1 kinase. https://app.cochat.ai/papers/10.1101/gad.6.4.545
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Bruder, J. T., Heidecker, G., & Rapp, U. R. (1992). Serum-, TPA-, and Ras-induced expression from Ap-1/Ets-driven promoters requires Raf-1 kinase. Genes & Development. https://doi.org/10.1101/gad.6.4.545

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