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Ras target proteins in eukaryotic cells
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 PKCζ. This review will attempt to sum‐marize the current literature of accepted and potential Ras‐dependent signaling proteins in both lower eukaryotes and vertebrates.—Marshall, M. S. Ras target proteins in eukaryotic cells. FASEB J . 9, 1311‐1318(1995)
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Cites
Phosphatidylinositol-3-OH kinase direct target of Ras
Rodriguez-Viciana, P., Warne, P. H., Dhand, R., Vanhaesebroeck, B., Gout, I., Fry, M. J., Waterfield, M. D., & Downward, J. (1994) · Nature · doi:10.1038/370527a0 · Cited by 1,954
Activated Ras interacts with the Ral guanine nucleotide dissociation stimulator.
Hofer, F., Fields, S., Schneider, C., & Martin, G. S. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.23.11089 · Cited by 287
Cited by
Raetz, C. R. H., & Whitfield, C. (2002) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.71.110601.135414 · Cited by 4,404
Post-translational modifications in signal integration
Deribe, Y. L., Pawson, T., & Dikic, I. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1842 · Cited by 876
Importance of Glucose-6-phosphate Dehydrogenase Activity for Cell Growth
Tian, W.-N., Braunstein, L. D., Pang, J., Stuhlmeier, K. M., Xi, Q.-C., Tian, X., & Stanton, R. C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.17.10609 · Cited by 532
Opposing Effects of Ras on p53
Ries, S., Biederer, C., Woods, D., Shifman, O., Shirasawa, S., Sasazuki, T., McMahon, M., Oren, M., & McCormick, F. (2000) · Cell · doi:10.1016/s0092-8674(00)00123-9 · Cited by 357
The Lipooligosaccharides of Pathogenic Gram-Negative Bacteria
Preston, A., Mandrell, R. E., Gibson, B. W., & Apicella, M. A. (1996) · Critical Reviews in Microbiology · doi:10.3109/10408419609106458 · Cited by 318
Metadata
- Authors
- Marshall, M. S.
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 1995-10
- Volume
- 9
- Issue
- 13
- Pages
- 1311-1318
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W1491629634
- Cited by
- 309
- References
- 2
- FWCI
- 11.96
- Type
- journal article
- Language
- en
- Open access
- closed
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