Hunter Chris J, Remenyi Judit, Correa Sonia A, Privitera Lucia, Reyskens Kathleen M S E, Martin Kirsty J, Toth Rachel, Frenguelli Bruno G, Arthur J Simon C
MRC Protein Phosphorylation Unit College of Life Sciences Sir James Black Centre University of Dundee UK.
Wellcome Trust Centre for Gene Regulation and Expression Wellcome Trust Building College of Life Sciences University of Dundee UK.
FEBS Open Bio. 2017 May 11;7(6):821-834. doi: 10.1002/2211-5463.12232. eCollection 2017 Jun.
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).
即刻早期基因活性调节细胞骨架蛋白(Arc)/Arg3.1和神经营养因子脑源性神经营养因子(BDNF)在哺乳动物大脑的突触可塑性、学习和记忆中发挥重要作用。然而,BDNF调节Arc/Arg3.1表达的机制尚不清楚。在本研究中,我们发现BDNF通过ERK1/2通路激活核激酶丝裂原和应激激活蛋白激酶1(MSK1)。然后,MSK1通过在Arc/Arg3.1启动子处使组蛋白H3磷酸化来诱导Arc/Arg3.1表达。MSK1还可以使转录因子环磷腺苷反应元件结合蛋白(CREB)的Ser133位点磷酸化。然而,这对于BDNF诱导的Arc.Arg3.1转录并非必需,因为Ser133Ala敲入突变对Arc/Arg3.1的诱导没有影响。同时,ERK1/2通过启动子上至少一个血清反应元件直接激活Arc/Arg3.1 mRNA转录,该元件与血清反应因子(SRF)和三元复合因子(TCF)的复合物结合。