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BDNF-induced local translation of GluA1 is regulated by HNRNP A2/B1

机译:BDNF诱导的Glua1局部翻译由HNRNP A2 / B1调节

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The AMPA receptor subunit GluA1 is essential for induction of synaptic plasticity. While various regulatory mechanisms of AMPA receptor expression have been identified, the underlying mechanisms of GluA1 protein synthesis are not fully understood. In neurons, axonal and dendritic mRNAs have been reported to be translated in a cap-independent manner. However, molecular mechanisms of cap-independent translation of synaptic mRNAs remain largely unknown. Here, we show that GluA1 mRNA contains an internal ribosome entry site (IRES) in the 5′UTR. We also demonstrate that heterogeneous nuclear ribonucleoprotein (hnRNP) A2/B1 interacts with GluA1 mRNA and mediates internal initiation of GluA1 . Brain-derived neurotrophic factor (BDNF) stimulation increases IRES-mediated GluA1 translation via up-regulation of HNRNP A2/B1. Moreover, BDNF-induced GluA1 expression and dendritic spine density were significantly decreased in neurons lacking hnRNP A2/B1. Together, our data demonstrate that IRES-mediated translation of GluA1 mRNA is a previously unidentified feature of local expression of the AMPA receptor.
机译:AMPA受体亚单位Glua1对于诱导突触塑性是必不可少的。虽然已经确定了AMPA受体表达的各种调节机制,但GLUA1蛋白质合成的潜在机制尚未完全理解。在神经元中,据报道,已讨论轴突和树突MRNA以独立的方式翻译。然而,突触突然翻译的突触MRNA的分子机制仍然很大程度上是未知的。在这里,我们表明,5'UTR中含有内部核糖体入口部位(IRES)。我们还证明,异构核核糖核糖蛋白(HNRNP)A2 / B1与GLUA1 mRNA相互作用并介导GLUA1的内部开始。脑衍生的神经营养因子(BDNF)刺激通过HNRNP A2 / B1的上调增加了IRES介导的GLUA1平移。此外,在缺乏HNRNP A2 / B1的神经元中,BDNF诱导的Glua1表达和树突状脊柱密度显着降低。我们的数据在一起表明,Glua1 mRNA的IRE介导的翻译是AMPA受体局部表达的先前未识别的特征。

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