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Published on: December 15, 2017
Ras target proteins in eukaryotic cells
1Department of Medicine, Indiana University School of Medicine, Indianapolis 46202, USA.
Abstract:
The 21 kDa Ras proteins are well known for their regulatory role in oncogenic, mitogenic, and developmental signaling pathways. Less well understood are the downstream signal transduction cascades initiated by Ras in response to external stimuli. Only recently have many diverse studies in lower eukaryotes and vertebrates converged to demonstrate that Ras directly regulates multiple signaling pathways. In most eukaryotes, Ras functions as a positive regulator of an ERK/MAPK signal transduction cascade through the activation of a MEKK. In mammalian cells the primary Ras-responsive MEKK is the protein kinase Raf. Although Raf remains the most significant mediator of Ras signaling in most model systems, it does not explain all the biochemical responses observed in cells with activated Ras proteins. Yeast two hybrid and GST-fusion protein binding studies have identified new proteins distinct from Raf that could interact with Ras in other signaling pathways. In addition to Raf, other potential Ras target proteins include MEKK1, PI(3)K, p120GAP, ralGDS, and PKC zeta. This review will attempt to summarize the current literature of accepted and potential Ras-dependent signaling proteins in both lower eukaryotes and vertebrates.
Insights
Ras proteins regulate key cell pathways. While Raf is a major mediator, new research reveals other Ras-interacting proteins, expanding our understanding of Ras signaling networks.
Area of Science:
- Cellular Biology
- Molecular Biology
- Biochemistry
Background:
- Ras proteins (21 kDa) are crucial regulators of oncogenic, mitogenic, and developmental signaling.
- Downstream signal transduction cascades initiated by Ras are not fully understood.
- Recent studies indicate Ras directly regulates multiple signaling pathways across eukaryotes.
Purpose of the Study:
- To review accepted and potential Ras-dependent signaling proteins.
- To explore Ras interactions beyond the canonical Raf pathway.
- To synthesize findings from lower eukaryotes and vertebrates.
Main Methods:
- Literature review of diverse studies.
- Yeast two-hybrid assays.
- GST-fusion protein binding studies.
Main Results:
- Ras primarily activates ERK/MAPK cascades via MEKK, with Raf being the main mammalian MEKK.
- Raf does not account for all Ras-mediated biochemical responses.
- Identified potential Ras targets include MEKK1, PI(3)K, p120GAP, ralGDS, and PKC zeta.
Conclusions:
- Ras signaling is more complex than previously thought, involving multiple effectors.
- Understanding these diverse Ras-interacting proteins is key to deciphering its full biological role.
- This review consolidates current knowledge on Ras-dependent pathways.
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