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神经元中CREB的转录活性受多种钙特异性磷酸化事件的调控。

CREB transcriptional activity in neurons is regulated by multiple, calcium-specific phosphorylation events.

作者信息

Kornhauser Jon M, Cowan Christopher W, Shaywitz Adam J, Dolmetsch Ricardo E, Griffith Eric C, Hu Linda S, Haddad Chia, Xia Zhengui, Greenberg Michael E

机构信息

Division of Neuroscience, Children's Hospital and Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Neuron. 2002 Apr 11;34(2):221-33. doi: 10.1016/s0896-6273(02)00655-4.

Abstract

The transcription factor CREB mediates diverse responses in the nervous system. It is not known how CREB induces specific patterns of gene expression in response to different extracellular stimuli. We find that Ca(2+) influx into neurons induces CREB phosphorylation at Ser133 and two additional sites, Ser142 and Ser143. While CREB Ser133 phosphorylation is induced by many stimuli, phosphorylation at Ser142 and Ser143 is selectively activated by Ca(2+) influx. The triple phosphorylation of CREB is required for effective Ca(2+) stimulation of CREB-dependent transcription, but the phosphorylation of Ser142 and Ser143, in addition to Ser133, disrupts the interaction of CREB with its cofactor CBP. These results suggest that Ca(2+) influx triggers a specific program of gene expression in neurons by selectively regulating CREB phosphorylation.

摘要

转录因子CREB介导神经系统中的多种反应。目前尚不清楚CREB如何响应不同的细胞外刺激诱导特定的基因表达模式。我们发现钙离子流入神经元会诱导CREB在Ser133以及另外两个位点Ser142和Ser143发生磷酸化。虽然许多刺激均可诱导CREB的Ser133磷酸化,但Ser142和Ser143的磷酸化是由钙离子流入选择性激活的。CREB的三重磷酸化是钙离子有效刺激CREB依赖性转录所必需的,但除Ser133外,Ser142和Ser143的磷酸化会破坏CREB与其辅因子CBP的相互作用。这些结果表明,钙离子流入通过选择性调节CREB磷酸化触发神经元中特定的基因表达程序。

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