Literature DB >> 7568222

A general strategy for producing conditional alleles of Src-like tyrosine kinases.

D M Spencer1, I Graef, D J Austin, S L Schreiber, G R Crabtree.   

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.

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Year:  1995        PMID: 7568222      PMCID: PMC40891          DOI: 10.1073/pnas.92.21.9805

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  52 in total

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9.  Pre-Golgi degradation of newly synthesized T-cell antigen receptor chains: intrinsic sensitivity and the role of subunit assembly.

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10.  Selective degradation of T cell antigen receptor chains retained in a pre-Golgi compartment.

Authors:  C Chen; J S Bonifacino; L C Yuan; R D Klausner
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  21 in total

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6.  Targeted expansion of genetically modified bone marrow cells.

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7.  A versatile synthetic dimerizer for the regulation of protein-protein interactions.

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8.  Proximity and orientation underlie signaling by the non-receptor tyrosine kinase ZAP70.

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9.  A proliferation switch for genetically modified cells.

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