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ShcD interacts with TrkB via its PTB and SH2 domains and regulates BDNF-induced MAPK activation

机译:ShcD通过其PTB和SH2结构域与TrkB相互作用,并调节BDNF诱导的MAPK激活

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摘要

Neurotrophins regulate many aspects of neuronal function through activation of the high affinity Irk receptors. Shc family proteins are implicated in the coupling of RTK to the Ras/mitogen-activated protein kinase signaling cascade. Here we report that the fourth Shc family member, ShcD, associates with TrkB receptor and regulates BDNF-induced MAPK activation. Yeast two-hybrid assay and Co-IP experiments demonstrate ShcD interacts with TrkB in a kinase-activity-dependent manner. Confocal analysis shows ShcD cololizes well with TrkB in transfected 293T cells. Subsequent mapping experiments and mutational analysis indicate that both PTB and SH2 domains are capable of binding to TrkB and PTB domain binds to TrkB NPQY motif. Furthermore, ShcD is involved in BDNF-induced MAPK activation. In summary, we demonstrate that ShcD is a substrate of TrkB and mediates TrkB downstream signaling pathway. [BMB reports 2010; 43(7): 485-490]
机译:神经营养蛋白通过激活高亲和力Irk受体来调节神经元功能的许多方面。 Shc家族蛋白与RTK与Ras /丝裂原活化的蛋白激酶信号级联反应的偶联有关。在这里,我们报告说,第四个Shc家族成员ShcD与TrkB受体缔合,并调节BDNF诱导的MAPK激活。酵母双杂交测定法和Co-IP实验证明ShcD与TrkB相互作用呈激酶活性依赖性。共聚焦分析显示,ShcD与TrkB在转染的293T细胞中很好地结合。随后的作图实验和突变分析表明,PTB和SH2结构域均能够与TrkB结合,而PTB结构域则与TrkB NPQY基序结合。此外,ShcD参与BDNF诱导的MAPK激活。总之,我们证明ShcD是TrkB的底物并介导TrkB下游信号传导途径。 [BMB报告2010; 43(7):485-490]

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