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核因子I在小脑颗粒神经元基因表达的内在调控中的作用。

A role for nuclear factor I in the intrinsic control of cerebellar granule neuron gene expression.

作者信息

Wang Wei, Stock Rachel E, Gronostajski Richard M, Wong Yong Wee, Schachner Melitta, Kilpatrick Daniel L

机构信息

University of Massachusetts Medical School, Department of Molecular and Cellular Physiology, 55 Lake Ave N., Worcester, MA 01655, USA.

出版信息

J Biol Chem. 2004 Dec 17;279(51):53491-7. doi: 10.1074/jbc.M410370200. Epub 2004 Oct 1.

Abstract

Nervous system formation requires the elaboration of a complex series of differentiation events in both a spatially and maturation-regulated manner. A fundamental question is how neuronal subtype specification and developmental gene expression are controlled within maturing neurons. The alpha6 subunit of the gamma-aminobutyric acid type A (GABA(A)) receptor (GABRA6) is preferentially expressed in cerebellar granule neurons and is part of an intrinsic program directing their differentiation. We have employed a lentiviral approach to examine the transcriptional mechanisms controlling neuronal subtype-selective expression of this gene. These studies demonstrated that nuclear factor I (NFI) proteins are required for both transgenic GABRA6 promoter activity as well as endogenous expression of this gene in cerebellar granule neurons. Chromatin immunoprecipitation also showed that NFI proteins are bound to the GABRA6 promoter in these cells in vivo. Furthermore, analyses of gene knockout mice revealed that Nfia is specifically required for normal expression of the GABRA6 gene in cerebellar granule neurons. NFI expression and DNA binding activity are highly enriched in granule neurons, implicating this transcription factor family in the neuronal subtype-selective expression of the GABRA6 gene. These studies define a new role for NFI proteins as neuronal subtype-enriched transcriptional regulators that participate in an intrinsic transcriptional program directing the differentiation of cerebellar granule neurons.

摘要

神经系统的形成需要以空间和成熟度调节的方式精心安排一系列复杂的分化事件。一个基本问题是,在成熟神经元中,神经元亚型的特异性和发育基因的表达是如何受到控制的。γ-氨基丁酸A型(GABA(A))受体(GABRA6)的α6亚基在小脑颗粒神经元中优先表达,并且是指导其分化的内在程序的一部分。我们采用慢病毒方法来研究控制该基因神经元亚型选择性表达的转录机制。这些研究表明,核因子I(NFI)蛋白对于转基因GABRA6启动子活性以及该基因在小脑颗粒神经元中的内源性表达都是必需的。染色质免疫沉淀还表明,NFI蛋白在体内与这些细胞中的GABRA6启动子结合。此外,对基因敲除小鼠的分析表明,Nfia对于小脑颗粒神经元中GABRA6基因的正常表达是特异性必需的。NFI的表达和DNA结合活性在颗粒神经元中高度富集,这表明该转录因子家族参与了GABRA6基因的神经元亚型选择性表达。这些研究确定了NFI蛋白作为神经元亚型富集的转录调节因子的新作用,其参与指导小脑颗粒神经元分化的内在转录程序。

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