MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function

被引:221
作者
Barbosa, Ana C. [1 ]
Kim, Mi-Sung [1 ]
Ertunc, Mert [2 ]
Adachi, Megumi [3 ]
Nelson, Erika D. [3 ]
McAnally, John [1 ]
Richardson, James A. [4 ]
Kavalali, Ege T. [2 ]
Monteggia, Lisa M. [3 ]
Bassel-Duby, Rhonda [1 ]
Olson, Eric N. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Psychiat, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
关键词
synaptic transmission; synaptogenesis; learning deficits;
D O I
10.1073/pnas.0802679105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Learning and memory depend on the activity-dependent structural plasticity of synapses and changes in neuronal gene expression. We show that deletion of the MEF2C transcription factor in the CNS of mice impairs hippocampal-dependent learning and memory. Unexpectedly, these behavioral changes were accompanied by a marked increase in the number of excitatory synapses and potentiation of basal and evoked synaptic transmission. Conversely, neuronal expression of a superactivating form of MEF2C results in a reduction of excitatory postsynaptic sites without affecting learning and memory performance. We conclude that MEF2C limits excessive synapse formation during activity-dependent refinement of synaptic connectivity and thus facilitates hippocampal-dependent learning and memory.
引用
收藏
页码:9391 / 9396
页数:6
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