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Gene regulation via excitation and BDNF is mediated by induction and phosphorylation of the Etv1 transcription factor in cerebellar granule cells

机译:小脑颗粒细胞中Etv1转录因子的诱导和磷酸化介导通过兴奋和BDNF的基因调控

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In maturing postnatal cerebellar granule cells, the Etv1/Er81 transcription factor is induced by sequential activity-dependent mechanisms through stimulation of AMPA and NMDA receptors, voltage-dependent Nav1.2 Na~+ channels, and voltage-dependent Ca~(2+) channels. Etv1 then up-regulates a battery of maturation genes involved in the cerebellar circuitry. In this process, BDNF is also induced and participates in the up-regulation of these maturation genes. Using cultures of granule cells, we addressed how the activity-dependent and BDNF signaling mechanisms converge on the regulation of the representative NR2C NMDA receptor and Tiami maturation genes. BDNF up-regulated both the NR2C and Tiami genes via the TrkB-Erk cascade and this up-regulation was blocked not only by inhibition of the activity-dependent signaling mechanisms but also by suppression of Etv1 expression with Etv1 siRNA. Importantly, Etv1 was selectively phosphorylated by Erk1/2 in the BDNF signaling cascade, and the inhibition of this phosphorylation abrogated the BDNF-induced up-regulation of the NR2C and Tiami genes. The luciferase reporter assays in combination with mutations of MEK and Etv1 indicated that the Erk-mediated, phosphorylated Etv1 interacted with the Ets motifs of the NR2C promoter sequence and that phosphorylation at both serine 94 and a cluster of threonines and a serine (Thr139, Thr143, and Ser146) of Etv1 was indispensable for the BDNF-mediated activation of the NR2C promoter activity. This study demonstrates that the NR2C and Tiami maturation genes are synergistically controlled by the activity-dependent induction of Etv1 and its phosphorylation by the BDNF signaling cascade.
机译:在成熟的产后小脑颗粒细胞中,Etv1 / Er81转录因子通过刺激AMPA和NMDA受体,电压依赖性Nav1.2 Na〜+通道和电压依赖性Ca〜(2+)的顺序活动依赖性机制来诱导。渠道。然后,Etv1上调与小脑电路有关的一系列成熟基因。在这个过程中,BDNF也被诱导并参与这些成熟基因的上调。使用颗粒细胞的培养,我们探讨了活性依赖性和BDNF信号传导机制如何在代表性NR2C NMDA受体和Tiami成熟基因的调控上融合。 BDNF通过TrkB-Erk级联上调了NR2C和Tiami基因,不仅抑制了活性依赖性信号传导机制,而且还抑制了Etv1 siRNA的表达,从而阻止了该上调。重要的是,Etv1在BDNF信号级联反应中被Erk1 / 2选择性地磷酸化,而对这种磷酸化的抑制则废除了BDNF诱导的NR2C和Tiami基因的上调。荧光素酶报告基因检测结合MEK和Etv1的突变表明,Erk介导的磷酸化Etv1与NR2C启动子序列的Ets模体相互作用,丝氨酸94以及苏氨酸和丝氨酸簇的磷酸化(Thr139,Thr143 (和Ser146)的表达对于BDNF介导的NR2C启动子活性的激活是必不可少的。这项研究表明,NR2C和Tiami成熟基因受Etv1的活性依赖性诱导及其BDNF信号级联的磷酸化的协同控制。

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