HISTONE DEACETYLASE 9 AS A NEGATIVE REGULATOR FOR CHOLINE ACETYLTRANSFERASE GENE IN NG108-15 NEURONAL CELLS

被引:16
作者
Aizawa, S. [1 ]
Teramoto, K. [1 ]
Yamamuro, Y. [1 ]
机构
[1] Nihon Univ, Coll Bioresource Sci, Dept Anim Sci, Lab Anim Genet & Physiol, Fujisawa, Kanagawa 2520880, Japan
基金
日本学术振兴会;
关键词
histone deacetylase 9; histone deacetylase inhibitor; choline acetyltransferase; cholinergic neuron; NG108-15; cells; GLIOMA HYBRID CLONE; TRANSCRIPTION FACTOR; SYNAPSE FORMATION; VALPROIC ACID; DIFFERENTIATION; INHIBITORS; EXPRESSION; ENHANCER; BINDING; CREB;
D O I
10.1016/j.neuroscience.2011.12.024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The biological function of histone deacetylases (HDACs), namely, repression of gene expression by removing an acetyl group from a histone N-terminal tail, plays an important role in numerous biological processes such as cell cycle, differentiation, and apoptosis in the development of individual tissues, including the brain. We previously showed the possible role of HDAC activity in the regulation of gene expression of choline acetyltransferase (ChAT), a specific marker for cholinergic neurons and their function, in NG108-15 neuronal cells as an in vitro model of cholinergic neurons. The objectives of the present study were to specify key HDACs and investigate the essential role of HDACs in ChAT gene regulation in NG108-15 cells. The experiments using different types of HDAC inhibitors indicated that class Ila HDACs substantially participate in the regulation of ChAT gene expression. In addition, HDAC9, a class Ila enzyme, was dramatically decreased at the protein levels, and dissociated from the promoter region of ChAT gene during neuronal differentiation. Furthermore, knockdown of HDAC9 by siRNA increased ChAT gene expression in undifferentiated cells. These findings demonstrate that HDAC9 is responsible for repressing ChAT gene expression in NG108-15 neuronal cells, and thus plays an important role in cholinergic differentiation. (C) 2012 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:63 / 72
页数:10
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