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Mammalian ELAV-like neuronal RNA-binding proteins HuB and HuC promote neuronal development in both the central and the peripheral nervous systems

机译:哺乳动物ELAV样神经元RNA结合蛋白HuB和HuC促进中枢和周围神经系统的神经元发育

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摘要

Hu proteins are mammalian embryonic lethal abnormal visual system (ELAV)-like neuronal RNA-binding proteins that contain three RNA recognition motifs. Although Drosophila ELAV is required for the correct differentiation and survival of neurons, the roles played by the Hu genes in the mammalian nervous system remain largely unknown. To explore the in vivo functions of mouse Hu proteins, we overexpressed them in rat pheochromocytoma PC12 cells, where they induced neuronal phenotype in the absence of nerve growth factor. We have characterized the functions of various forms of mHuB and mHuC bearing point mutations or deletions. Mutants of mHuC that had amino acid exchanges in the RNP1 domain of the first or second RNA recognition motifs (RRMs) lost biologic activity as well as RNA-binding activity. In addition, the mutants containing only the third RRM failed to induce the neuronal phenotype in PC12 cells and inhibited the biologic activity of cotransfected wild-type mHuB and mHuC, thus acting as a dominant-negative form. However, these mutants could not suppress the nerve growth factor-induced differentiation of PC12 cells. Further, we misexpressed wild-type and dominant-negative Hu in E9.5 mouse embryos, by using electroporation into the neural tube at the level of the rhombencephalon. mHuB and mHuC induced the ectopic expression of neuronal markers, whereas the dominant-negative forms of mHuB and mHuC suppressed the differentiation of central nervous system motor neurons. From these results, we suggest that Hu proteins are required for neuronal differentiation in the mammalian nervous system.
机译:Hu蛋白是包含三个RNA识别基序的哺乳动物胚胎致死异常视觉系统(ELAV)样神经元RNA结合蛋白。尽管果蝇ELAV是神经元正确分化和存活所必需的,但Hu基因在哺乳动物神经系统中所起的作用仍然未知。为了探索小鼠Hu蛋白的体内功能,我们在大鼠嗜铬细胞瘤PC12细胞中过表达了它们,它们在没有神经生长因子的情况下诱导了神经元表型。我们已经表征了各种形式的mHuB和mHuC轴承点突变或缺失的功能。在第一个或第二个RNA识别基序(RRM)的RNP1域中具有氨基酸交换的mHuC突变体失去了生物学活性以及RNA结合活性。此外,仅包含第三个RRM的突变体未能诱导PC12细胞中的神经元表型,并抑制了共转染的野生型mHuB和mHuC的生物活性,因此成为显性阴性形式。但是,这些突变体不能抑制神经生长因子诱导的PC12细胞分化。此外,通过使用电穿孔进入菱形脑水平的神经管,我们在E9.5小鼠胚胎中错误表达了野生型和显性负性Hu。 mHuB和mHuC诱导神经元标志物的异位表达,而mHuB和mHuC的显性负型抑制中枢神经系统运动神经元的分化。从这些结果,我们建议Hu蛋白是哺乳动物神经系统中神经元分化所必需的。

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