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首页> 外文期刊>FEBS Open Bio >MSK1 regulates transcriptional induction of Arc/Arg3.1 in response to neurotrophins
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MSK1 regulates transcriptional induction of Arc/Arg3.1 in response to neurotrophins

机译:MSK1调节响应神经营养蛋白的Arc / Arg3.1的转录诱导。

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The immediate early gene activity‐regulated cytoskeletal protein (Arc)/Arg3.1 and the neurotrophin brain‐derived neurotrophic factor (BDNF) play important roles in synaptic plasticity and learning and memory in the mammalian brain. However, the mechanisms by which BDNF regulates the expression of Arc/Arg3.1 are unclear. In this study, we show that BDNF acts via the ERK1/2 pathway to activate the nuclear kinase mitogen‐ and stress‐activated protein kinase 1 (MSK1). MSK1 then induces Arc/Arg3.1 expression via the phosphorylation of histone H3 at the Arc/Arg3.1 promoter. MSK1 can also phosphorylate the transcription factor cyclic‐AMP response element‐binding protein (CREB) on Ser133. However, this is not required for BDNF‐induced Arc.Arg3.1 transcription as a Ser133Ala knockin mutation had no effect on Arc/Arg3.1 induction. In parallel, ERK1/2 directly activates Arc/Arg3.1 mRNA transcription via at least one serum response element on the promoter, which bind a complex of the Serum Response Factor (SRF) and a Ternary Complex Factor (TCF).
机译:立即早期基因活性调节的细胞骨架蛋白(Arc)/Arg3.1和神经营养蛋白脑源性神经营养因子(BDNF)在哺乳动物脑中的突触可塑性和学习记忆中起重要作用。但是,BDNF调节Arc / Arg3.1表达的机制尚不清楚。在这项研究中,我们表明BDNF通过ERK1 / 2途径激活核激酶有丝分裂原和应激激活的蛋白激酶1(MSK1)。然后,MSK1通过在Arc / Arg3.1启动子处组蛋白H3的磷酸化诱导Arc / Arg3.1表达。 MSK1还可以磷酸化Ser133上的转录因子环-AMP反应元件结合蛋白(CREB)。但是,这对于BDNF诱导的Arc.Arg3.1转录不是必需的,因为Ser133Ala敲入突变对Arc / Arg3.1的诱导没有影响。同时,ERK1 / 2通过启动子上的至少一个血清反应元件直接激活Arc / Arg3.1 mRNA转录,该元件结合血清反应因子(SRF)和三元复合因子(TCF)的复合物。

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