| Literature DB >> 10637231 |
D Barilá1, R Mangano, S Gonfloni, J Kretzschmar, M Moro, D Bohmann, G Superti-Furga.
Abstract
The nuclear function of the c-Abl tyrosine kinase is not well understood. In order to identify nuclear substrates of Abl, we constructed a constitutively active and nuclear form of the protein. We found that active nuclear Abl efficiently phosphorylate c-Jun, a transcription factor not previously known to be tyrosine phosphorylated. After phosphorylation of c-Jun by Abl on Tyr170, both proteins interacted via the SH2 domain of Abl. Surprisingly, elevated levels of c-Jun activated nuclear Abl, resulting in activation of the JNK serine/threonine kinase. This phosphorylation circuit generates nuclear tyrosine phosphorylation and represents a reversal of previously known signalling models.Entities:
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Year: 2000 PMID: 10637231 PMCID: PMC305561 DOI: 10.1093/emboj/19.2.273
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598