Characterization of proteins that interact with the cell-cycle regulatory protein Ran/TC4 - PubMed (original) (raw)
. 1993 Dec 9;366(6455):585-7.
doi: 10.1038/366585a0.
Affiliations
- PMID: 8255297
- DOI: 10.1038/366585a0
Characterization of proteins that interact with the cell-cycle regulatory protein Ran/TC4
E Coutavas et al. Nature. 1993.
Abstract
The human Ras-related nuclear protein Ran/TC4 (refs 1-4) is the prototype of a well conserved family of GTPases that can regulate both cell-cycle progression and messenger RNA transport. Ran has been proposed to undergo tightly controlled cycles of GTP binding and hydrolysis, to operate as a GTPase switch whose GTP- and GDP-bound forms interact differentially with regulators and effectors. One known regulator, the protein RCC1 (refs 12, 13), interacts with Ran to catalyse guanine nucleotide exchange, and both RCC1 and Ran are components of an intrinsic checkpoint control that prevents the premature initiation of mitosis. To test and extend the GTPase-switch model, we searched for a Ran-specific GTPase-activating protein (GAP), and for putative effectors (proteins that interact specifically with Ran/TC4-GTP). We report here the identification of a Ran GAP and its use to characterize the GTP-hydrolysing properties of mutant Ran proteins, and the identification and cloning of a binding protein specific for Ran/TC4-GTP.
Similar articles
- Catalysis of guanine nucleotide exchange on Ran by the mitotic regulator RCC1.
Bischoff FR, Ponstingl H. Bischoff FR, et al. Nature. 1991 Nov 7;354(6348):80-2. doi: 10.1038/354080a0. Nature. 1991. PMID: 1944575 - RNA1 encodes a GTPase-activating protein specific for Gsp1p, the Ran/TC4 homologue of Saccharomyces cerevisiae.
Becker J, Melchior F, Gerke V, Bischoff FR, Ponstingl H, Wittinghofer A. Becker J, et al. J Biol Chem. 1995 May 19;270(20):11860-5. doi: 10.1074/jbc.270.20.11860. J Biol Chem. 1995. PMID: 7744835 - Model of the ran-RCC1 interaction using biochemical and docking experiments.
Azuma Y, Renault L, García-Ranea JA, Valencia A, Nishimoto T, Wittinghofer A. Azuma Y, et al. J Mol Biol. 1999 Jun 18;289(4):1119-30. doi: 10.1006/jmbi.1999.2820. J Mol Biol. 1999. PMID: 10369786 - Spi1 GTPase interacts with RCC1 to maintain interdependency of cell cycle events.
Matsumoto T, Beach D. Matsumoto T, et al. Princess Takamatsu Symp. 1991;22:145-52. Princess Takamatsu Symp. 1991. PMID: 1844237 Review. - [Cell cycle regulation and Ran/TC4 GTPase].
Nishimoto T. Nishimoto T. Tanpakushitsu Kakusan Koso. 1996 Sep;41(12 Suppl):1906-12. Tanpakushitsu Kakusan Koso. 1996. PMID: 8890654 Review. Japanese. No abstract available.
Cited by
- Genetic variation in the 22q11 locus and susceptibility to schizophrenia.
Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ, Roos JL, Rapoport JL, Gogos JA, Karayiorgou M. Liu H, et al. Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16859-64. doi: 10.1073/pnas.232186099. Epub 2002 Dec 11. Proc Natl Acad Sci U S A. 2002. PMID: 12477929 Free PMC article. - Calcium Regulates the Nuclear Localization of Protein Arginine Deiminase 2.
Zheng L, Nagar M, Maurais AJ, Slade DJ, Parelkar SS, Coonrod SA, Weerapana E, Thompson PR. Zheng L, et al. Biochemistry. 2019 Jul 9;58(27):3042-3056. doi: 10.1021/acs.biochem.9b00225. Epub 2019 Jun 27. Biochemistry. 2019. PMID: 31243954 Free PMC article. - Unloading RNAs in the cytoplasm: an "importin" task.
Dias SM, Cerione RA, Wilson KF. Dias SM, et al. Nucleus. 2010 Mar-Apr;1(2):139-43. doi: 10.4161/nucl.1.2.10919. Epub 2009 Dec 2. Nucleus. 2010. PMID: 21326945 Free PMC article. Review. - Selective impairment of a subset of Ran-GTP-binding domains of ran-binding protein 2 (Ranbp2) suffices to recapitulate the degeneration of the retinal pigment epithelium (RPE) triggered by Ranbp2 ablation.
Patil H, Saha A, Senda E, Cho KI, Haque M, Yu M, Qiu S, Yoon D, Hao Y, Peachey NS, Ferreira PA. Patil H, et al. J Biol Chem. 2014 Oct 24;289(43):29767-89. doi: 10.1074/jbc.M114.586834. Epub 2014 Sep 3. J Biol Chem. 2014. PMID: 25187515 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous