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A Nuclear Function of Hu Proteins as Neuron-specific Alternative RNA Processing Regulators

机译:胡蛋白的核功能作为神经元特异性替代RNA加工调节剂。

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摘要

Recent advances in genome-wide analysis of alternative splicing indicate that extensive alternative RNA processing is associated with many proteins that play important roles in the nervous system. Although differential splicing and polyadenylation make significant contributions to the complexity of the nervous system, our understanding of the regulatory mechanisms underlying the neuron-specific pathways is very limited. Mammalian neuron-specific embryonic lethal abnormal visual-like Hu proteins (HuB, HuC, and HuD) are a family of RNA-binding proteins implicated in neuronal differentiation and maintenance. It has been established that Hu proteins increase expression of proteins associated with neuronal function by up-regulating mRNA stability and/or translation in the cytoplasm. We report here a novel function of these proteins as RNA processing regulators in the nucleus. We further elucidate the underlying mechanism of this regulation. We show that in neuron-like cells, Hu proteins block the activity of TIA-1/TIAR, two previously identified, ubiquitously expressed proteins that promote the nonneuronal pathway of calcitonin/calcitonin gene-related peptide (CGRP) pre-mRNA processing. These studies define not only the first neuron-specific regulator of the calcitonin/CGRP system but also the first nuclear function of Hu proteins.
机译:替代剪接的全基因组分析的最新进展表明,广泛的替代RNA处理与许多在神经系统中起重要作用的蛋白质有关。尽管差异剪接和聚腺苷酸化对神经系统的复杂性做出了重要贡献,但我们对神经元特异性途径的调控机制的了解非常有限。哺乳动物神经元特异性胚胎致死性异常视觉样Hu蛋白(HuB,HuC和HuD)是一类涉及神经元分化和维持的RNA结合蛋白。已经证实,Hu蛋白通过上调mRNA的稳定性和/或在细胞质中的翻译来增加与神经元功能相关的蛋白的表达。我们在这里报告这些蛋白质作为核中RNA加工调节剂的新型功能。我们进一步阐明了该法规的基本机制。我们显示,在神经元样细胞中,Hu蛋白会阻断TIA-1 / TIAR的活性,TIA-1 / TIAR是两个先前确定的,泛在表达的蛋白,它们促进降钙素/降钙素基因相关肽(CGRP)的非神经途径通路的mRNA加工。这些研究不仅定义了降钙素/ CGRP系统的第一个神经元特异性调节剂,而且定义了Hu蛋白的第一个核功能。

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