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调节 Tau 蛋白亚细胞定位作为研究疾病相关基因表达的一种工具。

Modulation of Tau Subcellular Localization as a Tool to Investigate the Expression of Disease-related Genes.

作者信息

Siano Giacomo, Caiazza Maria Claudia, Varisco Martina, Calvello Mariantonietta, Quercioli Valentina, Cattaneo Antonino, Di Primio Cristina

机构信息

Laboratory of Biology, BIO@SNS, Scuola Normale Superiore.

Laboratory of Biology, BIO@SNS, Scuola Normale Superiore;

出版信息

J Vis Exp. 2019 Dec 20(154). doi: 10.3791/59988.

Abstract

Tau is a microtubule binding protein expressed in neurons and its main known function is related to the maintenance of cytoskeletal stability. However, recent evidence indicated that Tau is present also in other subcellular compartments including the nucleus where it is implicated in DNA protection, in rRNA transcription, in the mobility of retrotransposons and in the structural organization of the nucleolus. We have recently demonstrated that nuclear Tau is involved in the expression of the VGluT1 gene, suggesting a molecular mechanism that could explain the pathological increase of glutamate release in the early stages of Alzheimer's disease. Until recently, the involvement of nuclear Tau in modulating the expression of target genes has been relatively uncertain and ambiguous due to technical limitations that prevented the exclusion of the contribution of cytoplasmic Tau or the effect of other downstream factors not related to nuclear Tau. To overcome this uncertainty, we developed a method to study the expression of target genes specifically modulated by the nuclear Tau protein. We employed a protocol that couples the use of localization signals and the subcellular fractionation, allowing the exclusion of the interference from the cytoplasmic Tau molecules. Most notably, the protocol is easy and is composed of classic and reliable methods that are broadly applicable to study the nuclear function of Tau in other cell types and cellular conditions.

摘要

Tau是一种在神经元中表达的微管结合蛋白,其主要已知功能与维持细胞骨架稳定性有关。然而,最近的证据表明,Tau也存在于其他亚细胞区室中,包括细胞核,在细胞核中它与DNA保护、rRNA转录、逆转录转座子的移动性以及核仁的结构组织有关。我们最近证明,核Tau参与了VGluT1基因的表达,提示了一种分子机制,该机制可以解释阿尔茨海默病早期谷氨酸释放的病理性增加。直到最近,由于技术限制,无法排除细胞质Tau的贡献或其他与核Tau无关的下游因素的影响,核Tau在调节靶基因表达中的作用一直相对不确定且模糊。为了克服这种不确定性,我们开发了一种方法来研究由核Tau蛋白特异性调节的靶基因的表达。我们采用了一种将定位信号的使用与亚细胞分级分离相结合的方案,从而排除了细胞质Tau分子的干扰。最值得注意的是,该方案简单易行,由经典且可靠的方法组成,广泛适用于研究Tau在其他细胞类型和细胞条件下的核功能。

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