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The Etv1/Er81 transcription factor orchestrates activity-dependent gene regulation in the terminal maturation program of cerebellar granule cells

机译:Etv1 / Er81转录因子在小脑颗粒细胞的终末成熟程序中协调活动依赖的基因调节

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In the postnatal period, cerebellar granule cells express a set of the maturation gene battery in an activity-dependent manner and establish synaptic function in the cerebellar circuitry. Using primary cultures combined with specific inhibition of signaling cascades, the present investigation revealed that the expression of the maturation genes, including the NMDA glutamate receptor NR2C and GABA_A receptor GABA_ARa6 genes, is controlled by strikingly unified signaling mechanisms that operate sequentially through stimulation of AiyiPA and NMDA receptors, Na~+ channels [voltage-gated Na channel type II (Nav1.2)], and voltage-dependent Ca~(2+) channels. This signaling then induces the Ets variant gene 1 (Etv1/Er81) transcription factor of the ETS family in an activity-dependent manner. Consistent with the culture study, the ChIP assay indicated that Etv1 up-regulates the maturation genes in a developmentally regulated manner. This activation, as revealed by the luciferase assay, occurrs by interacting with the Etv1-interacting motifs present in the promoter region. Importantly, in vivo knockdown of Etv1 by DNA electroporation in the developing cerebellum prevents the up-regulation of the maturation genes but has no effects on preceding developmental processes occurring in the granule cells. Etv1 thus orchestrates the activity-dependent gene regulation in the terminal maturation program and specifies the identity of cerebellar granule cells.
机译:在出生后,小脑颗粒细胞以活动依赖的方式表达一组成熟基因电池,并在小脑回路中建立突触功能。使用原代培养结合信号传导级联的特异性抑制,本研究表明,成熟基因(包括NMDA谷氨酸受体NR2C和GABA_A受体GABA_ARa6基因)的表达受到惊人统一信号机制的控制,该机制通过刺激AiyiPA和NMDA受体,Na〜+通道[电压门控Na通道II型(Nav1.2)]和电压依赖性Ca〜(2+)通道。然后,该信号传导以活性依赖的方式诱导ETS家族的Ets变异基因1(Etv1 / Er81)转录因子。与培养研究一致,ChIP分析表明Etv1以发育调控的方式上调成熟基因。如荧光素酶测定所揭示的,这种活化是通过与启动子区域中存在的与Etv1相互作用的基序相互作用而发生的。重要的是,在发育中的小脑中通过DNA电穿孔对Etv1进行体内敲除可防止成熟基因的上调,但对颗粒细胞中发生的先前发育过程没有影响。因此,Etv1会在最终成熟程序中协调活动相关基因的调控,并指定小脑颗粒细胞的身份。

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