Activity-dependent transcription regulation of PSD-95 by neuregulin-1 and Eos

被引:128
作者
Bao, JX [1 ]
Lin, H
Ouyang, Y
Lei, DB
Osman, A
Kim, TW
Mei, L
Dai, PG
Ohlemiller, KK
Ambron, RT
机构
[1] Washington Univ, Dept Otolaryngol, St Louis, MO 63110 USA
[2] Washington Univ, Ctr Aging, St Louis, MO 63110 USA
[3] Washington Univ, Dept Neurol, St Louis, MO 63110 USA
[4] Columbia Univ, Dept Anat & Cell Biol, New York, NY 10032 USA
[5] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[6] Med Coll Georgia, Dept Neurol, Inst Mol Med & Genet, Augusta, GA 30912 USA
关键词
D O I
10.1038/nn1342
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuregulin-1 (Nrg-1) contains an intracellular domain (Nrg-ICD) that translocates into the nucleus, where it may regulate gene expression upon neuronal depolarization. However, the identity of its target promoters and the mechanisms by which it regulates transcription have been elusive. Here we report that, in the mouse cochlea, synaptic activity increases the level of nuclear Nrg-ICD and upregulates postsynaptic density protein-95 (PSD-95), a scaffolding protein that is enriched in post-synaptic structures. Nrg-ICD enhances the transcriptional activity of the PSD-95 promoter by binding to a zinc-finger transcription factor, Eos. The Nrg-ICD-Eos complex induces endogenous PSD-95 expression in vivo through a signaling pathway that is mostly independent of gamma-secretase regulation. This upregulation of PSD-95 expression by the Nrg-ICD- Eos complex provides a molecular basis for activity-dependent synaptic plasticity.
引用
收藏
页码:1250 / 1258
页数:9
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