RACGAP1: Difference between revisions

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RACGAP1 has been shown to [[Protein-protein interaction|interact]] with [[Rnd2]]<ref name=pmid12590651>{{cite journal | vauthors = Naud N, Touré A, Liu J, Pineau C, Morin L, Dorseuil O, Escalier D, Chardin P, Gacon G | title = Rho family GTPase Rnd2 interacts and co-localizes with MgcRacGAP in male germ cells | journal = The Biochemical Journal | volume = 372 | issue = Pt 1 | pages = 105–12 | date = May 2003 | pmid = 12590651 | pmc = 1223378 | doi = 10.1042/BJ20021652 }}</ref> and [[SLC26A8]].<ref name=pmid11278976>{{cite journal | vauthors = Toure A, Morin L, Pineau C, Becq F, Dorseuil O, Gacon G | title = Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling | journal = The Journal of Biological Chemistry | volume = 276 | issue = 23 | pages = 20309–15 | date = June 2001 | pmid = 11278976 | doi = 10.1074/jbc.M011740200 }}</ref>
RACGAP1 has been shown to [[Protein-protein interaction|interact]] with [[Rnd2]]<ref name=pmid12590651>{{cite journal | vauthors = Naud N, Touré A, Liu J, Pineau C, Morin L, Dorseuil O, Escalier D, Chardin P, Gacon G | title = Rho family GTPase Rnd2 interacts and co-localizes with MgcRacGAP in male germ cells | journal = The Biochemical Journal | volume = 372 | issue = Pt 1 | pages = 105–12 | date = May 2003 | pmid = 12590651 | pmc = 1223378 | doi = 10.1042/BJ20021652 }}</ref> and [[SLC26A8]].<ref name=pmid11278976>{{cite journal | vauthors = Toure A, Morin L, Pineau C, Becq F, Dorseuil O, Gacon G | title = Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling | journal = The Journal of Biological Chemistry | volume = 276 | issue = 23 | pages = 20309–15 | date = June 2001 | pmid = 11278976 | doi = 10.1074/jbc.M011740200 }}</ref>


During cytokinesis, RACGAP1 has been shown to interact with [[KIF23]] to form the [[centralspindlin]] complex.<ref name="cytokinesis">{{cite journal | vauthors = Glotzer M | title = Cytokinesis: centralspindlin moonlights as a membrane anchor | journal = Current Biology | volume = 23 | issue = 4 | pages = R145-7 | date = February 2013 | pmid = 23428321 | doi = 10.1016/j.cub.2013.01.006 }}</ref>  This complex is essential for the formation of the central spindle. RACGAP1 also interacts with [[PRC1]] to stabilize and maintain the central spindle as anaphase proceeds.<ref>{{cite journal | vauthors = Lee KY, Esmaeili B, Zealley B, Mishima M | title = Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle | journal = Nature Communications | volume = 6 | pages = 7290 | date = 2015 | pmid = 26088160 | doi = 10.1038/ncomms8290 | pmc=4557309}}</ref>
During cytokinesis, RACGAP1 has been shown to interact with [[KIF23]] to form the [[centralspindlin]] complex.<ref name="cytokinesis">{{cite journal | vauthors = Glotzer M | title = Cytokinesis: centralspindlin moonlights as a membrane anchor | journal = Current Biology | volume = 23 | issue = 4 | pages = R145–7 | date = February 2013 | pmid = 23428321 | doi = 10.1016/j.cub.2013.01.006 }}</ref>  This complex is essential for the formation of the central spindle. RACGAP1 also interacts with [[PRC1]] to stabilize and maintain the central spindle as anaphase proceeds.<ref>{{cite journal | vauthors = Lee KY, Esmaeili B, Zealley B, Mishima M | title = Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle | journal = Nature Communications | volume = 6 | pages = 7290 | date = 2015 | pmid = 26088160 | doi = 10.1038/ncomms8290 | pmc=4557309}}</ref>


== References ==
== References ==
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== Further reading ==
== Further reading ==
{{Refbegin|33em}}
{{Refbegin|33em}}
* {{cite journal | vauthors = Maruyama K, Sugano S | title = Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides | journal = Gene | volume = 138 | issue = 1-2 | pages = 171–4 | date = January 1994 | pmid = 8125298 | doi = 10.1016/0378-1119(94)90802-8 }}
* {{cite journal | vauthors = Maruyama K, Sugano S | title = Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides | journal = Gene | volume = 138 | issue = 1–2 | pages = 171–4 | date = January 1994 | pmid = 8125298 | doi = 10.1016/0378-1119(94)90802-8 }}
* {{cite journal | vauthors = Gerwins P, Blank JL, Johnson GL | title = Cloning of a novel mitogen-activated protein kinase kinase kinase, MEKK4, that selectively regulates the c-Jun amino terminal kinase pathway | journal = The Journal of Biological Chemistry | volume = 272 | issue = 13 | pages = 8288–95 | date = March 1997 | pmid = 9079650 | doi = 10.1074/jbc.272.13.8288 }}
* {{cite journal | vauthors = Gerwins P, Blank JL, Johnson GL | title = Cloning of a novel mitogen-activated protein kinase kinase kinase, MEKK4, that selectively regulates the c-Jun amino terminal kinase pathway | journal = The Journal of Biological Chemistry | volume = 272 | issue = 13 | pages = 8288–95 | date = March 1997 | pmid = 9079650 | doi = 10.1074/jbc.272.13.8288 }}
* {{cite journal | vauthors = Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S | title = Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library | journal = Gene | volume = 200 | issue = 1-2 | pages = 149–56 | date = October 1997 | pmid = 9373149 | doi = 10.1016/S0378-1119(97)00411-3 }}
* {{cite journal | vauthors = Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S | title = Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library | journal = Gene | volume = 200 | issue = 1–2 | pages = 149–56 | date = October 1997 | pmid = 9373149 | doi = 10.1016/S0378-1119(97)00411-3 }}
* {{cite journal | vauthors = ((Nagata Ki)), Puls A, Futter C, Aspenstrom P, Schaefer E, Nakata T, Hirokawa N, Hall A | title = The MAP kinase kinase kinase MLK2 co-localizes with activated JNK along microtubules and associates with kinesin superfamily motor KIF3 | journal = The EMBO Journal | volume = 17 | issue = 1 | pages = 149–58 | date = January 1998 | pmid = 9427749 | pmc = 1170366 | doi = 10.1093/emboj/17.1.149 }}
* {{cite journal | vauthors = ((Nagata Ki)), Puls A, Futter C, Aspenstrom P, Schaefer E, Nakata T, Hirokawa N, Hall A | title = The MAP kinase kinase kinase MLK2 co-localizes with activated JNK along microtubules and associates with kinesin superfamily motor KIF3 | journal = The EMBO Journal | volume = 17 | issue = 1 | pages = 149–58 | date = January 1998 | pmid = 9427749 | pmc = 1170366 | doi = 10.1093/emboj/17.1.149 }}
* {{cite journal | vauthors = Tapon N, Nagata K, Lamarche N, Hall A | title = A new rac target POSH is an SH3-containing scaffold protein involved in the JNK and NF-kappaB signalling pathways | journal = The EMBO Journal | volume = 17 | issue = 5 | pages = 1395–404 | date = March 1998 | pmid = 9482736 | pmc = 1170487 | doi = 10.1093/emboj/17.5.1395 }}
* {{cite journal | vauthors = Tapon N, Nagata K, Lamarche N, Hall A | title = A new rac target POSH is an SH3-containing scaffold protein involved in the JNK and NF-kappaB signalling pathways | journal = The EMBO Journal | volume = 17 | issue = 5 | pages = 1395–404 | date = March 1998 | pmid = 9482736 | pmc = 1170487 | doi = 10.1093/emboj/17.5.1395 }}

Latest revision as of 13:44, 7 November 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Rac GTPase-activating protein 1 is an enzyme that in humans is encoded by the RACGAP1 gene.[1]

Function

Rho GTPases control a variety of cellular processes. There are 3 subtypes of Rho GTPases in the Ras superfamily of small G proteins: RHO (see MIM 165370), RAC (see RAC1; MIM 602048), and CDC42 (MIM 116952). GTPase-activating proteins (GAPs) bind activated forms of Rho GTPases and stimulate GTP hydrolysis. Through this catalytic function, Rho GAPs negatively regulate Rho-mediated signals. GAPs may also serve as effector molecules and play a role in signaling downstream of Rho and other Ras-like GTPases.[supplied by OMIM][2]

Interactions

RACGAP1 has been shown to interact with Rnd2[3] and SLC26A8.[4]

During cytokinesis, RACGAP1 has been shown to interact with KIF23 to form the centralspindlin complex.[5] This complex is essential for the formation of the central spindle. RACGAP1 also interacts with PRC1 to stabilize and maintain the central spindle as anaphase proceeds.[6]

References

  1. Touré A, Dorseuil O, Morin L, Timmons P, Jégou B, Reibel L, Gacon G (March 1998). "MgcRacGAP, a new human GTPase-activating protein for Rac and Cdc42 similar to Drosophila rotundRacGAP gene product, is expressed in male germ cells". The Journal of Biological Chemistry. 273 (11): 6019–23. doi:10.1074/jbc.273.11.6019. PMID 9497316.
  2. "Entrez Gene: RACGAP1 Rac GTPase activating protein 1".
  3. Naud N, Touré A, Liu J, Pineau C, Morin L, Dorseuil O, Escalier D, Chardin P, Gacon G (May 2003). "Rho family GTPase Rnd2 interacts and co-localizes with MgcRacGAP in male germ cells". The Biochemical Journal. 372 (Pt 1): 105–12. doi:10.1042/BJ20021652. PMC 1223378. PMID 12590651.
  4. Toure A, Morin L, Pineau C, Becq F, Dorseuil O, Gacon G (June 2001). "Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling". The Journal of Biological Chemistry. 276 (23): 20309–15. doi:10.1074/jbc.M011740200. PMID 11278976.
  5. Glotzer M (February 2013). "Cytokinesis: centralspindlin moonlights as a membrane anchor". Current Biology. 23 (4): R145–7. doi:10.1016/j.cub.2013.01.006. PMID 23428321.
  6. Lee KY, Esmaeili B, Zealley B, Mishima M (2015). "Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle". Nature Communications. 6: 7290. doi:10.1038/ncomms8290. PMC 4557309. PMID 26088160.

Further reading