Organization of the mouse Ruk locus and expression of isoforms in mouse tissues
- PMID: 12242006
- DOI: 10.1016/s0378-1119(02)00821-1
Organization of the mouse Ruk locus and expression of isoforms in mouse tissues
Abstract
Ruk is a recently identified gene with a complex pattern of expression in mammalian cells and tissues. Multiple Ruk transcripts and several protein isoforms have been detected in various types of cells. Ruk proteins have multidomain organization characteristic of adapter proteins involved in regulation of signal transduction. Interaction of some Ruk isoforms with several signalling proteins, including the p85 regulatory subunit of the Class IA PI 3-kinase, c-Cbl and Grb2, has been demonstrated. Ruk(l), an isoform with three SH3 domains, inhibits lipid kinase activity of the PI 3-kinase in vitro; overexpression of this protein induces apoptotic cell death of primary neurons in culture and changes in membrane trafficking in other cultured cells. However, shorter isoforms of Ruk block pro-apoptotic effect of Ruk(l), suggesting that expression of different combinations of Ruk proteins in cells could be involved in the regulation of their survival and other intracellular processes. To understand the mechanism of differential expression of Ruk proteins we studied organization of the mouse Ruk gene and its transcripts. Twenty-four exons of the Ruk gene span over 320 kb of the mouse chromosome X. Analysis of cDNA clones, ESTs and products of RT-PCR amplifications with different combinations of primers revealed how alternative splicing and promoter usage generate a variety of Ruk transcripts and encoded protein isoforms in different mouse tissues.
Similar articles
-
Negative regulation of PI 3-kinase by Ruk, a novel adaptor protein.EMBO J. 2000 Aug 1;19(15):4015-25. doi: 10.1093/emboj/19.15.4015. EMBO J. 2000. PMID: 10921882 Free PMC article.
-
Ruk is ubiquitinated but not degraded by the proteasome.Eur J Biochem. 2002 Jul;269(14):3402-8. doi: 10.1046/j.1432-1033.2002.03031.x. Eur J Biochem. 2002. PMID: 12135478
-
Multiple domains of Ruk/CIN85/SETA/CD2BP3 are involved in interaction with p85alpha regulatory subunit of PI 3-kinase.J Mol Biol. 2004 Oct 29;343(4):1135-46. doi: 10.1016/j.jmb.2004.08.075. J Mol Biol. 2004. PMID: 15476827
-
Expression of adaptor protein Ruk/CIN85 isoforms in cell lines of various tissue origins and human melanoma.Exp Oncol. 2006 Dec;28(4):275-81. Exp Oncol. 2006. PMID: 17285110
-
Emerging roles of Ruk/CIN85 in vesicle-mediated transport, adhesion, migration and malignancy.Traffic. 2010 Jun;11(6):721-31. doi: 10.1111/j.1600-0854.2010.01061.x. Epub 2010 Mar 17. Traffic. 2010. PMID: 20331533 Review.
Cited by
-
Hunk/Mak-v is a negative regulator of intestinal cell proliferation.BMC Cancer. 2015 Mar 8;15:110. doi: 10.1186/s12885-015-1087-2. BMC Cancer. 2015. PMID: 25881306 Free PMC article.
-
Porcine reproductive and respiratory syndrome virus nonstructural protein 2 promotes the autophagic degradation of adaptor protein SH3KBP1 to antagonize host innate immune responses by enhancing K63-linked polyubiquitination of RIG-I.PLoS Pathog. 2024 Oct 28;20(10):e1012670. doi: 10.1371/journal.ppat.1012670. eCollection 2024 Oct. PLoS Pathog. 2024. PMID: 39466846 Free PMC article.
-
Alix/AIP1 antagonizes epidermal growth factor receptor downregulation by the Cbl-SETA/CIN85 complex.Mol Cell Biol. 2004 Oct;24(20):8981-93. doi: 10.1128/MCB.24.20.8981-8993.2004. Mol Cell Biol. 2004. PMID: 15456872 Free PMC article.
-
CIN85 Deficiency Prevents Nephrin Endocytosis and Proteinuria in Diabetes.Diabetes. 2016 Dec;65(12):3667-3679. doi: 10.2337/db16-0081. Epub 2016 Aug 16. Diabetes. 2016. PMID: 27531950 Free PMC article.
-
CIN85/RukL is a novel binding partner of nephrin and podocin and mediates slit diaphragm turnover in podocytes.J Biol Chem. 2010 Aug 13;285(33):25285-95. doi: 10.1074/jbc.M109.087239. Epub 2010 May 10. J Biol Chem. 2010. PMID: 20457601 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Research Materials
Miscellaneous