MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function
Author(s) -
Ana C. Barbosa,
Mi-Sung Kim,
Mert Ertunç,
Megumi Adachi,
Erika D. Nelson,
John McAnally,
James A. Richardson,
Ege T. Kavalali,
Lisa M. Monteggia,
Rhonda BasselDuby,
Eric N. Olson
Publication year - 2008
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0802679105
Subject(s) - neuroscience , long term potentiation , synapse , excitatory postsynaptic potential , biology , postsynaptic potential , mef2c , synaptic plasticity , neuronal memory allocation , transcription factor , hippocampal formation , neurotransmission , excitatory synapse , hippocampus , memory consolidation , inhibitory postsynaptic potential , synaptic augmentation , genetics , gene , receptor
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.
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