Effect of the ubiquitous transcription factors, SP1 and MAZ, on NMDA receptor subunit type 1 (NR1) expression during neuronal differentiation

被引:61
作者
Okamoto, S
Sherman, K
Bai, G
Lipton, SA
机构
[1] Burnham Inst, Ctr Neurosci & Aging, La Jolla, CA 92037 USA
[2] Brigham & Womens Hosp, Cerebrovasc & NeuroSci Res Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
来源
MOLECULAR BRAIN RESEARCH | 2002年 / 107卷 / 02期
关键词
NMDA receptor; neurogenesis; NRSF/REST; SP1; MAZ;
D O I
10.1016/S0169-328X(02)00440-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The silencer factor NRSF/REST has been reported to restrict expression to neurons of a variety of genes, including that encoding NMDA receptor subunit type 1 (NR 1), by suppressing transcription in nonneuronal cells. However, we recently reported that in addition to the absence of NRSF/REST-binding activity, another neuron-specific mechanism is necessary for high level expression of the NR1 gene in neurons. In this study. we explored the mechanism of induction of NR1 promoter activity during neuronal differentiation of the P19 cell line. We identified a 27 base pair GC-rich region in the promoter as an important element responsible for induction of the NR1 gene after neuronal differentiation. We found that the ubiquitous transcription factors SP1 and MAZ bind to this GC-rich region. Surprisingly, the binding activities of SP1 and MAZ are not remarkably changed after neuronal differentiation. Mutations in the SP1 and MAZ sites impair binding of SP1 and MAZ proteins and also decrease NR1 promoter activity. These findings suggest that SP1 and MAZ mediate enhancement of NR1 promoter activity during neuronal differentiation despite the fact that their binding activity does not change. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:89 / 96
页数:8
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