A general strategy for producing conditional alleles of Src-like tyrosine kinases
- PMID: 7568222
- PMCID: PMC40891
- DOI: 10.1073/pnas.92.21.9805
A general strategy for producing conditional alleles of Src-like tyrosine kinases
Abstract
The Src-like tyrosine kinases require membrane localization for transformation and probably for their normal role in signal transduction. We utilized this characteristic to prepare Src-like tyrosine kinases that can be readily activated with the rationally designed chemical inducer of dimerization FK1012. Dimerization of cytoplasmic Src-like tyrosine kinases was not sufficient for signaling, but their recruitment to the plasma membrane led to the rapid activation of transcription factors identical to those regulated by crosslinking the antigen receptor. Moreover, recruitment of activated Src-like kinases to the membrane replaced signaling by the T-lymphocyte antigen receptor complex, leading to the activation of both the Ras/protein kinase C and Ca2+/calcineurin pathways normally activated by antigen receptor signaling. Since these chemical inducers of dimerization are cell permeable, this approach permits the production of conditional alleles of any of the Src-like tyrosine kinases, thereby allowing a delineation of their developmental roles.
Similar articles
-
Differences in binding of PI 3-kinase to the src-homology domains 2 and 3 of p56 lck and p59 fyn tyrosine kinases.Biochem Biophys Res Commun. 1996 Mar 27;220(3):729-34. doi: 10.1006/bbrc.1996.0472. Biochem Biophys Res Commun. 1996. PMID: 8607833
-
Regulation of cytotoxic T lymphocyte-associated molecule-4 by Src kinases.J Immunol. 1999 Feb 1;162(3):1270-7. J Immunol. 1999. PMID: 9973379
-
Platelet-derived growth factor (PDGF)-induced activation of signal transducer and activator of transcription (Stat) 5 is mediated by PDGF beta-receptor and is not dependent on c-src, fyn, jak1 or jak2 kinases.Biochem J. 2000 Feb 1;345 Pt 3(Pt 3):759-66. Biochem J. 2000. PMID: 10642538 Free PMC article.
-
Positive and negative regulation of T-cell activation through kinases and phosphatases.Biochem J. 2003 Apr 1;371(Pt 1):15-27. doi: 10.1042/BJ20021637. Biochem J. 2003. PMID: 12485116 Free PMC article. Review.
-
The p60c-src family of protein-tyrosine kinases: structure, regulation, and function.Crit Rev Oncog. 1992;3(4):401-46. Crit Rev Oncog. 1992. PMID: 1384720 Review.
Cited by
-
Proximity-Based Modalities for Biology and Medicine.ACS Cent Sci. 2023 Jul 14;9(7):1269-1284. doi: 10.1021/acscentsci.3c00395. eCollection 2023 Jul 26. ACS Cent Sci. 2023. PMID: 37521793 Free PMC article. Review.
-
Controlled dimerization of ErbB receptors provides evidence for differential signaling by homo- and heterodimers.Mol Cell Biol. 1999 Oct;19(10):6845-57. doi: 10.1128/MCB.19.10.6845. Mol Cell Biol. 1999. PMID: 10490623 Free PMC article.
-
Latent membrane protein 1 of Epstein-Barr virus mimics a constitutively active receptor molecule.EMBO J. 1997 Oct 15;16(20):6131-40. doi: 10.1093/emboj/16.20.6131. EMBO J. 1997. PMID: 9359753 Free PMC article.
-
Synthetic activation of caspases: artificial death switches.Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3655-60. doi: 10.1073/pnas.95.7.3655. Proc Natl Acad Sci U S A. 1998. PMID: 9520421 Free PMC article.
-
Proximity-induced membrane protein degradation for cancer therapies.RSC Med Chem. 2025 May 2. doi: 10.1039/d5md00141b. Online ahead of print. RSC Med Chem. 2025. PMID: 40365034 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous