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Regulation and Role of Raf-1/B-Raf Heterodimerization

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Rushworth, Linda K., Hindley, Alison D., O'Neill, Eric, Kolch, Walter·2006·Molecular and Cellular Biology

Abstract

The Ras-Raf-MEK-extracellular signal-regulated kinase (ERK) pathway participates in the control of many fundamental cellular processes including proliferation, survival, and differentiation. The pathway is deregulated in up to 30% of human cancers, often due to mutations in Ras and the B-Raf isoform. Raf-1 and B-Raf can form heterodimers, and this may be important for cellular transformation. Here, we have analyzed the biochemical and biological properties of Raf-1/B-Raf heterodimers. Isolated Raf-1/B-Raf heterodimers possessed a highly increased kinase activity compared to the respective homodimers or monomers. Heterodimers between wild-type Raf-1 and B-Raf mutants with low or no kinase activity still displayed elevated kinase activity, as did heterodimers between wild-type B-Raf and kinase-negative Raf-1. In contrast, heterodimers containing both kinase-negative Raf-1 and kinase-negative B-Raf were completely inactive, suggesting that the kinase activity of the heterodimer specifically originates from Raf and that either kinase-competent Raf isoform is sufficient to confer high catalytic activity to the heterodimer. In cell lines, Raf-1/B-Raf heterodimers were found at low levels. Heterodimerization was enhanced by 14-3-3 proteins and by mitogens independently of ERK. However, ERK-induced phosphorylation of B-Raf on T753 promoted the disassembly of Raf heterodimers, and the mutation of T753 prolonged growth factor-induced heterodimerization. The B-Raf T753A mutant enhanced differentiation of PC12 cells, which was previously shown to be dependent on sustained ERK signaling. Fine mapping of the interaction sites by peptide arrays suggested a complex mode of interaction involving multiple contact sites with a main Raf-1 binding site in B-Raf encompassing T753. In summary, our data suggest that Raf-1/B-Raf heterodimerization occurs as part of the physiological activation process and that the heterodimer has distinct biochemical properties that may be important for the regulation of some biological processes.

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Crossref · 10.1128/mcb.26.6.2262-2272.2006

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Metadata

Authors
Rushworth, L. K., Hindley, A. D., O'Neill, E., & Kolch, W.
Venue
Molecular and Cellular Biology
Published
2006-03
Volume
26
Issue
6
Pages
2262-2272
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
OpenAlex
W2123551753
Cited by
418
References
1
FWCI
8.47
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Regulation and Role of Raf-1/B-Raf Heterodimerization. https://app.cochat.ai/papers/10.1128/mcb.26.6.2262-2272.2006
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Rushworth, L. K., Hindley, A. D., O'Neill, E., & Kolch, W. (2006). Regulation and Role of Raf-1/B-Raf Heterodimerization. Molecular and Cellular Biology. https://doi.org/10.1128/mcb.26.6.2262-2272.2006

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