奶油
激酶
磷酸化
钙调蛋白
去极化
细胞生物学
生物
转录因子
化学
生物化学
分子生物学
生物物理学
基因
酶
作者
Morgan Sheng,Margaret A. Thompson,Michael E. Greenberg
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1991-06-07
卷期号:252 (5011): 1427-1430
被引量:1482
标识
DOI:10.1126/science.1646483
摘要
The mechanism by which Ca 2+ mediates gene induction in response to membrane depolarization was investigated. The adenosine 3′,5′-monophosphate (cAMP) response element-binding protein (CREB) was shown to function as a Ca 2+ -regulated transcription factor and as a substrate for depolarization-activated Ca 2+ -calmodulin-dependent protein kinases (CaM kinases) I and II. CREB residue Ser 133 was the major site of phosphorylation by the CaM kinases in vitro and of phosphorylation after membrane depolarization in vivo. Mutation of Ser 133 impaired the ability of CREB to respond to Ca 2+ . These results suggest that CaM kinases may transduce electrical signals to the nucleus and that CREB functions to integrate Ca 2+ and cAMP signals.
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