Drosophila C-terminal Src kinase negatively regulates organ growth and cell proliferation through inhibition of the Src, Jun N-terminal kinase, and STAT pathways
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作者:
Read, RD
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机构:Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Read, RD
Bach, EA
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机构:Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Bach, EA
Cagan, RL
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机构:Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
Cagan, RL
机构:
[1] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[2] NYU, Sch Med, Dept Pharmacol, New York, NY 10012 USA
Src family kinases regulate multiple cellular processes including proliferation and oncogenesis. C-terminal Src kinase (Csk) encodes a critical negative regulator of Sire family kinases. We demonstrate that the Drosophila melanogaster Csk ortholog, dCsk, functions as a tumor suppressor: dCsk mutants display organ overgrowth and excess cellular proliferation. Genetic analysis indicates that the dCsk(-/-) overgrowth phenotype results from activation of Src, Jun kinase, and STAT signal transduction pathways. In particular, blockade of STAT function in dCsk mutants severely reduced Sirc-dependent overgrowth and activated apoptosis of mutant tissue. Our data provide in vivo evidence that Src activity requires JNK and STAT function.