Regulation of CBP-mediated transcription by neuronal calcium signaling

被引:197
作者
Hu, SC
Chrivia, J
Ghosh, A [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] St Louis Univ, Dept Pharmacol & Physiol Sci, St Louis, MO 63104 USA
关键词
D O I
10.1016/S0896-6273(00)80738-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The transcription factor CREB is involved in mediating many of the long-term effects of activity-dependent plasticity at glutamatergic synapses. Here, we show that activation of NMDA receptors and voltage-sensitive calcium channels leads to CREB-mediated transcription in cortical neurons via a mechanism regulated by CREB-binding protein (CBP). Recruitment of CBP to the promoter is not sufficient for transactivation, but calcium influx can induce CBP-mediated transcription via two distinct transactivation domains. CBP-mediated transcription is stimulus strength-dependent and can be induced by activation of CaM kinase II, CaM kinase IV, and protein kinase A, but not by activation of the Ras-MAP kinase pathway. These observations indicate that CBP can function as a calcium-sensitive transcriptional coactivator that may act as a regulatory switch for glutamate-induced CREB-mediated transcription.
引用
收藏
页码:799 / 808
页数:10
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