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The molecular basis of the specificity and cross-reactivity of the NeuN epitope of the neuron-specific splicing regulator, Rbfox3

机译:神经元特异性剪接调节剂Rbfox3的NeuN表位的特异性和交叉反应性的分子基础

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摘要

Ever since its description and the generation of its defining antibody, some 20 years ago, neural nuclei (NeuN) have been an invaluable tool for developmental neuroscientists and neuropathologists to identify neurons and follow their normal or malignant development. The recent identification of the splicing factor Rbfox3 as the molecule constituting the genuine NeuN epitope has opened up a novel perspective on NeuN immunostaining and its interpretation. Here, we briefly review these recent developments, and we provide a series of data that allow to rationalize the specificity of the NeuN/A60 antibody on aldehyde-fixed tissues on the one hand, and its cross-reactivity with Synapsin I and R3hdm2 on Western blots on the other. We argue that rather than being considered as a mere marker for mature neurons, Rbfox3-mediated NeuN/A60 immunoreactivity may provide a window onto neuronal biology. Specifically, we hypothesize that the phosphorylation-dependent antigenicity of the Rbfox3/NeuN epitope should allow to visualize neuronal physiology realized through Rbfox3, including splicing, on the single-cell level.
机译:自从其描述和定义抗体的产生以来,大约20年前,神经核(NeuN)一直是发育中的神经科学家和神经病理学家识别神经元并遵循其正常或恶性发展的宝贵工具。剪接因子Rbfox3作为构成真正NeuN表位的分子的最新鉴定为NeuN免疫染色及其解释开辟了新的视角。在这里,我们简要回顾这些最新进展,并提供一系列数据,一方面可以使NeuN / A60抗体在醛固定组织上的特异性合理化,并且可以与Western上的Synapsin I和R3hdm2的交叉反应性在另一个上的污点。我们认为,Rbfox3介导的NeuN / A60免疫反应性可能不仅仅被视为成熟神经元的标记,还可能为神经元生物学提供一个窗口。具体来说,我们假设Rbfox3 / NeuN表位的磷酸化依赖性抗原性应允许在单细胞水平上可视化通过Rbfox3实现的神经元生理学,包括剪接。

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