Ras (protein)
371659
223392635
2008-07-03T21:51:57Z
193.165.105.72
/* Attachments */
{{dablink|This article is about the Ras family of proteins. For other meanings see the [[Ras (disambiguation)]] page.}}
{{Pfam_box
| Symbol = Ras
| Name =
| image = Ras-Structure.png
| width =250
| caption = Triphosphate Structure of H-Ras p21 GNBP in complex with GppNHp and Mg<sup>2+</sup> (PDB Code 5p21). Important sequence elements are highlighted.
| Pfam= PF00071
| InterPro= IPR013753
| SMART=
| PROSITE = PDOC00859
| SCOP = 5p21
| TCDB =
| OPM family=
| OPM protein= 1uad
| PDB=
{{PDB3|2fol}}A:13-174 {{PDB3|1ukv}}Y:10-171 {{PDB3|1yzn}}A:10-171
{{PDB3|2bcg}}Y:10-171 {{PDB3|1g17}}B:22-182 {{PDB3|1g16}}C:22-182
{{PDB3|3rab}}A:24-185 {{PDB3|1zbd}}A:24-185 {{PDB3|2ew1}}A:11-172
{{PDB3|1x3s}}A:10-171 {{PDB3|1z0k}}A:10-171 {{PDB3|2bme}}A:10-171
{{PDB3|2bmd}}A:10-171 {{PDB3|1yu9}}A:10-171 {{PDB3|2aed}}A:13-174
{{PDB3|1z0f}}A:13-174 {{PDB3|1z0a}}D:8-169 {{PDB3|2a5j}}A:8-169
{{PDB3|1oiv}}B:13-172 {{PDB3|1yzk}}A:13-174 {{PDB3|1oix}}A:13-172
{{PDB3|1oiw}}A:13-172 {{PDB3|1z06}}A:35-201 {{PDB3|1huq}}A:23-182
{{PDB3|1z0d}}C:23-183 {{PDB3|1z07}}A:23-182 {{PDB3|1r2q}}A:22-183
{{PDB3|1n6r}}A:22-183 {{PDB3|1ek0}}A:9-173 {{PDB3|1yvd}}A:7-168
{{PDB3|1z0j}}A:7-168 {{PDB3|2fg5}}A:7-168 {{PDB3|1z08}}A:21-182
{{PDB3|1yzt}}B:21-182 {{PDB3|1yzu}}B:21-182 {{PDB3|1z0i}}A:21-182
{{PDB3|1yzq}}A:15-176 {{PDB3|1d5c}}A:13-172 {{PDB3|1t91}}C:10-175
{{PDB3|1vg8}}D:10-175 {{PDB3|1vg9}}H:10-175 {{PDB3|1vg1}}A:10-175
{{PDB3|1vg0}}B:10-175 {{PDB3|1ky3}}A:10-178 {{PDB3|1ky2}}A:10-178
{{PDB3|1yzl}}A:9-174 {{PDB3|1wms}}B:9-174 {{PDB3|1s8f}}B:9-174
{{PDB3|2f7s}}A:11-183 {{PDB3|1z22}}A:11-171 {{PDB3|1z2a}}A:11-171
{{PDB3|1plj}} :5-165 {{PDB3|1ctq}}A:5-165 {{PDB3|1crp}} :5-165
{{PDB3|821p}} :5-165 {{PDB3|2ery}}B:16-177 {{PDB3|2fn4}}A:31-192
{{PDB3|1x1s}}A:15-177 {{PDB3|1x1r}}A:15-177 {{PDB3|1u90}}A:16-177
{{PDB3|1u8z}}A:16-177 {{PDB3|1u8y}}B:16-177 {{PDB3|1uad}}B:16-177
{{PDB3|2bov}}A:16-177 {{PDB3|2a78}}A:16-177 {{PDB3|3rap}}R:5-166
{{PDB3|1kao}} :5-166 {{PDB3|2rap}} :5-166 {{PDB3|1c1y}}A:5-167
{{PDB3|1gua}}A:5-167 {{PDB3|1xtr}}A:8-169 {{PDB3|1xtq}}A:8-169
{{PDB3|1xts}}A:8-169 {{PDB3|2erx}}B:9-171 {{PDB3|1a4r}}B:5-178
{{PDB3|1kmq}}A:7-180 {{PDB3|1tx4}}B:7-179 {{PDB3|1cxz}}A:7-180
{{PDB3|1m7b}}A:25-199 {{PDB3|1gwn}}A:25-199 {{PDB3|2bku}}A:12-170
{{PDB3|3ran}}A:12-170 {{PDB3|1qg4}}B:12-170 {{PDB3|1byu}}A:12-170
{{PDB3|2atv}}A:8-169
}}
In [[molecular biology]], '''''Ras''''' is the name of a [[protein]], the [[gene]] that encodes it, and the family and superfamily (''see [[Ras superfamily]]'') of proteins to which it belongs. The ras oncogene is a signal transduction protein, which means that it communicates signals to other cells. Sometimes a DNA mutation turns the signal permanently on, which leads to unlimited cell growth and cancer.<ref>[http://theoncologist.alphamedpress.org/cgi/content/full/4/3/263 David S. Goodsell, Physician Education: The Molecular Perspective: The ras Oncogene, The Oncologist, Vol. 4, No. 3, 263-264, June 1999] Introductory article on molecular biology of ras oncogene for physicians. Illustrated. Full text free.</ref> The Ras superfamily of small [[GTPase]]s includes the Ras, [[Rho/Rac|Rho]], [[ADP ribosylation factor|Arf]], [[Rab (G-protein)|Rab]], and [[Ran_(biology)|Ran]] families.
==History==
The ''RAS'' genes were first identified as the transforming [[oncogenes]], responsible for the cancer-causing activities of the Harvey (the ''HRAS'' oncogene) and Kirsten (''KRAS'') sarcoma viruses, by Edward M. Scolnick and colleagues at the National Institutes of Health (NIH). These viruses were discovered originally in rats during the 1960's by Jennifer Harvey and Werner Kirsten, respectively. In 1982, activated and transforming human ''RAS'' genes were discovered in human cancer cells by Geoffrey M. Cooper at Harvard, Mariano Barbacid and [[Stuart A. Aaronson|Stuart A. Aaronson]] at the NIH and by [[Robert Weinberg|Robert A. Weinberg]] of [[MIT]]. Subsequent studies identified a third human ''RAS'' gene, designated ''NRAS'', for its initial identification in human neuroblastoma cells.
==Functions==
The three human RAS genes encode highly related 188 to 189 amino acid proteins, designated [[HRAS|H-Ras]], [[NRAS|N-Ras]] and K-Ras4A and K-Ras4B (the two [[KRAS|K-Ras]] proteins arise from alternative gene splicing). Ras proteins function as binary molecular switches that control intracellular signaling networks. Ras-regulated [[Signal transduction|signal pathways]] control such processes as actin cytoskeletal integrity, proliferation, differentiation, cell adhesion, [[apoptosis]], and cell migration.
Ras and ras-related proteins are often deregulated in cancers, leading to increased invasion and [[metastasis]], and decreased apoptosis.
Ras activates a number of pathways but an especially important one seems to be the [[MAP kinase|mitogen-activated protein (MAP) kinases]], which themselves transmit signals downstream to other protein kinases and gene regulatory proteins.<ref name="Lodish">{{cite book | author=Lodish H, Berk A, Zipursky SL, Matsudaira P, Baltimore D, Darnell J | title=Molecular cell biology | publisher=W.H. Freeman | location=San Francisco | year=2000 | edition=4th | chapter=Chapter 25, Cancer | id=ISBN 0-7167-3706-X}}</ref>
==Activated and inactivated forms==
Ras is a [[G protein]] (specifically a [[small GTPase]]): a regulatory [[Guanosine triphosphate|GTP]] hydrolase that cycles between two conformations – an activated or inactivated form, respectively RAS-GTP and RAS-GDP.
It is ''activated'' by [[guanine exchange factors]] (GEFs, eg. [[CDC25]], [[SOS1]] and [[SOS2]], [[SDC25]] in [[yeast]]), which are themselves activated by mitogenic signals and through feedback from Ras itself. A GEF usually heightens the dissociation rate of the nucleotide – while not changing the association rate (effectively lower the affinity of the nucleotide) – thereby promoting its exchange. The cellular concentration of GTP is much higher than that of GDP so the exchange is usually GDP vs. GTP.
It is ''inactivated'' by [[GTPase-activating proteins]] (GAPs, the most frequently cited one being [[RasGAP]]), which increase the rate of GTP hydrolysis, returning RAS to its GDP-bound form, simultaneously releasing an [[inorganic phosphate]].
==Attachments==
Ras is attached to the [[cell membrane]] by [[prenylation]], and in health is a key component in many pathways which couple growth factor receptors to downstream [[mitosis|mitogenic]] effectors involved in cell proliferation or differentiation.<ref name="Reuter">{{cite journal | author=Reuter C, Morgan M, Bergmann L | title=Targeting the Ras signaling pathway: a rational, mechanism-based treatment for hematologic malignancies? | journal=Blood | volume=96 | issue=5 | pages=1655–69 | year=2000 | pmid=10961860}}</ref> The C-terminal [[CaaX box]] of Ras first gets farnesylated at its Cys residue in the cytosol and then inserted into the membrane of the [[endoplasmatic reticulum]]. The Tripeptid (aaX) is then cleaved from the C-terminus by a specific prenyl-protein specific endoprotease, the new C-terminus is then methylated by a [[methyltransferase]]. The so processed Ras is now transported to the [[plasma membrane]]. Most Ras forms are now further palmitoylated, while K-Ras with its long positively charged stretch interacts electrostaticly with the membrane.
==Ras in cancer==
Mutations in the Ras family of [[proto-oncogene]]s (comprising H-Ras, N-Ras and K-Ras) are very common, being found in 20% to 30% of all human tumours.<ref>{{cite journal | author=Bos J | title=ras oncogenes in human cancer: a review | journal=Cancer Res | volume=49 | issue=17 | pages=4682–9 | year=1989 | pmid=2547513}}</ref>
===Inappropriate activation of the gene ===
Inappropriate activation of the gene has been shown to play a key role in signal transduction, proliferation and malignant transformation.<ref name="Lodish"> </ref>
Mutations in a number of different genes as well as RAS itself can have this effect. [[Oncogene]]s such as p210BCR-ABL or the growth receptor erbB are upstream of Ras, so if they are constitutively activated their signals will transduce through Ras.
The [[tumour suppressor gene]] [[NF1]] encodes a Ras-GAP – its mutation in [[neurofibromatosis]] will mean that Ras is less likely to be inactivated. Ras can also be amplified, although this only occurs occasionally in tumours.
Finally, Ras oncogenes can be activated by point mutations so that its GTPase reaction can no longer be stimulated by GAP – this increases the half life of active Ras-GTP mutants.<ref name="Reuter"> </ref>
===Constitutively active Ras===
''Constitutively active Ras'' (''Ras<sup>D</sup>'') is one which contains mutations that prevent GTP hydrolysis, thus locking Ras in a permanently 'On' state.
The most common mutations are found at residue G12 in the [[P-loop]] and the catalytic residue Q61.
* The glycine to valine mutation at ''residue 12'' renders the GTPase domain of Ras insensitive to inactivation by GAP and thus stuck in the "on state". Ras requires a GAP for inactivation as it is a relatively poor catalyst on its own, as opposed to other G-domain-containing proteins such as the alpha subunit of heterotrimeric G proteins.
* ''Residue 61''<ref>[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164790&a=164790_AllelicVariant0002 Omim - Neuroblastoma Ras Viral Oncogene Homolog; Nras<!-- Bot generated title -->]</ref> is responsible for stabilizing the transition state for GTP hydrolysis. Because enzyme catalysis in general is achieved by lowering the energy barrier between substrate and product, mutation of Q61 necessarily reduces the rate of intrinsic Ras GTP hydrolysis to physiologically meaningless levels.
See also "dominant negative" mutants such as S17N and D119N.
==Human proteins containing Ras domain ==
[[ARHE]]; [[ARHGAP5]]; [[CDC42]]; [[DIRAS1]]; [[DIRAS2]]; [[DIRAS3]]; [[ERAS]]; [[GEM]];
[[GRLF1]]; [[HRAS]]; [[KRAS]]; [[LOC393004]]; [[MRAS]]; [[NKIRAS1]]; [[NRAS]]; [[RAB10]];
[[RAB11A]]; [[RAB11B]]; [[RAB12]]; [[RAB13]]; [[RAB14]]; [[RAB15]]; [[RAB17]]; [[RAB18]];
[[RAB19]]; [[RAB1A]]; [[RAB1B]]; [[RAB2]]; [[RAB20]]; [[RAB21]]; [[RAB22A]]; [[RAB23]];
[[RAB24]]; [[RAB25]]; [[RAB26]]; [[RAB27A]]; [[RAB27B]]; [[RAB28]]; [[RAB2B]]; [[RAB30]];
[[RAB31]]; [[RAB32]]; [[RAB33A]]; [[RAB33B]]; [[RAB34]]; [[RAB35]]; [[RAB36]]; [[RAB37]];
[[RAB38]]; [[RAB39]]; [[RAB39B]]; [[RAB3A]]; [[RAB3B]]; [[RAB3C]]; [[RAB3D]]; [[RAB40A]];
[[RAB40AL]]; [[RAB40B]]; [[RAB40C]]; [[RAB41]]; [[RAB42]]; [[RAB43]]; [[RAB4A]]; [[RAB4B]];
[[RAB5A]]; [[RAB5B]]; [[RAB5C]]; [[RAB6A]]; [[RAB6B]]; [[RAB6C]]; [[RAB7A]]; [[RAB7B]];
[[RAB7L1]]; [[RAB8A]]; [[RAB8B]]; [[RAB9]]; [[RAB9B]]; [[RABL2A]]; [[RABL2B]]; [[RABL4]];
[[RAC1]]; [[RAC2]]; [[RAC3]]; [[RALA]]; [[RALB]]; [[RAN]]; [[RANP1]]; [[RAP1A]];
[[RAP1B]]; [[RAP2A]]; [[RAP2B]]; [[RAP2C]]; [[RASD1]]; [[RASD2]]; [[RASEF]]; [[RASL11A]];
[[RASL12]]; [[RBJ]]; [[REM1]]; [[REM2]]; [[RERG]]; [[RHEB]]; [[RHEBL1]]; [[RHOA]];
[[RHOB]]; [[RHOBTB1]]; [[RHOBTB2]]; [[RHOC]]; [[RHOD]]; [[RHOF]]; [[RHOG]]; [[RHOH]];
[[RHOJ]]; [[RHOQ]]; [[RHOU]]; [[RHOV]]; [[RIT1]]; [[RIT2]]; [[RND1]]; [[RND2]];
[[RND3]]; [[RRAD]]; [[RRAS]]; [[RRAS2]]; [[TC4]];
==References==
<references/>
==External links==
* [http://www.ncic.cancer.ca/ncic/internet/mediareleaselist/0,,84658243_85783616_88058948_langId-en.html "Brain tumour findings offer hope of new strategy Canadian Cancer Society says" at ncic.cancer.ca]
* [http://arstechnica.com/news.ars/post/20031104-3072.html "Novel cancer treatment gets NCI support" at arstechnica.com]
* {{MeshName|ras+Proteins}}
* {{MeshName|ras+Genes}}
{{Oncogenes}}
{{GTPases}}
[[Category:G proteins]]
[[Category:Peripheral membrane proteins]]
[[Category:Oncogenes]]
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[[fr:Protéine Ras]]
[[it:Ras (proteina)]]
[[ur:راس (سالماتی حیاتیات)]]