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Disabled Is a Putative Adaptor Protein That Functions during Signaling by the Sevenless Receptor Tyrosine Kinase

机译:禁用的是一个推定的衔接蛋白在通过七重受体酪氨酸激酶发出信号的过程中起作用。

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摘要

DRK, the Drosophila homolog of the SH2-SH3 domain adaptor protein Grb2, is required during signaling by the sevenless receptor tyrosine kinase (SEV). One role of DRK is to provide a link between activated SEV and the Ras1 activator SOS. We have investigated the possibility that DRK performs other functions by identifying additional DRK-binding proteins. We show that the phosphotyrosine-binding (PTB) domain-containing protein Disabled (DAB) binds to the DRK SH3 domains. DAB is expressed in the ommatidial clusters, and loss of DAB function disrupts ommatidial development. Moreover, reduction of DAB function attenuates signaling by a constitutively activated SEV. Our biochemical analysis suggests that DAB binds SEV directly via its PTB domain, becomes tyrosine phosphorylated upon SEV activation, and then serves as an adaptor protein for SH2 domain-containing proteins. Taken together, these results indicate that DAB is a novel component of the SEV signaling pathway.
机译:DRK是SH2-SH3域衔接子蛋白Grb2的果蝇同源物,在无七味受体酪氨酸激酶(SEV)发出信号期间需要。 DRK的作用之一是提供激活的SEV与Ras1激活剂SOS之间的链接。我们已经研究了DRK通过鉴定其他DRK结合蛋白来执行其他功能的可能性。我们显示,磷酸酪氨酸结合(PTB)域包含蛋白质禁用(DAB)绑定到DRK SH3域。 DAB在脐带簇中表达,DAB功能丧失会破坏脐带的发育。而且,DAB功能的降低通过组成性激活的SEV减弱了信号传导。我们的生化分析表明,DAB通过其PTB结构域直接与SEV结合,在SEV活化后酪氨酸被磷酸化,然后用作含SH2结构域蛋白的衔接蛋白。两者合计,这些结果表明DAB是SEV信号传导途径的新组成部分。

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