A neuronal isoform of CPEB regulates local protein synthesis and stabilizes synapse-specific long-term facilitation in Aplysia

被引:321
|
作者
Si, K
Giustetto, M
Etkin, A
Hsu, R
Janisiewicz, AM
Miniaci, MC
Kim, JH
Zhu, HX
Kandel, ER
机构
[1] Columbia Univ, New York State Psychiat Inst, Coll Phys & Surg, Howard Hughes Med Inst, New York, NY 10032 USA
[2] Columbia Univ, New York State Psychiat Inst, Coll Phys & Surg, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
D O I
10.1016/S0092-8674(03)01021-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synapse-specific facilitation requires rapamycin-dependent local protein synthesis at the activated synapse. In Aplysia, rapamycin-dependent local protein synthesis serves two functions: (1) it provides a component of the mark at the activated synapse and thereby confers synapse specificity and (2) it stabilizes the synaptic growth associated with long-term facilitation. Here we report that a neuron-specific isoform of cytoplasmic polyadenylation element binding protein (CPEB) regulates this synaptic protein synthesis in an activity-dependent manner. Aplysia CPEB protein is upregulated locally at activated synapses, and it is needed not for the initiation but for the stable maintenance of long-term facilitation. We suggest that Aplysia CPEB is one of the stabilizing components of the synaptic mark.
引用
收藏
页码:893 / 904
页数:12
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