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MiR-26a and MiR-384-5p Are Required for LTP Maintenance and Spine Enlargement

Overview
Journal Nat Commun
Specialty Biology
Date 2015 Apr 11
PMID 25858512
Citations 50
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Abstract

Long-term potentiation (LTP) is a form of synaptic plasticity that results in enhanced synaptic strength. It is associated with the formation and enlargement of dendritic spines-tiny protrusions accommodating excitatory synapses. Both LTP and spine remodelling are crucial for brain development, cognition and the pathophysiology of neurological disorders. The role of microRNAs (miRNAs) in the maintenance of LTP, however, is not well understood. Using next-generation sequencing to profile miRNA transcriptomes, we demonstrate that miR-26a and miR-384-5p specifically affect the maintenance, but not induction, of LTP and different stages of spine enlargement by regulating the expression of RSK3. Using bioinformatics, we also examine the global effects of miRNA transcriptome changes during LTP on gene expression and cellular activities. This study reveals a novel miRNA-mediated mechanism for gene-specific regulation of translation in LTP, identifies two miRNAs required for long-lasting synaptic and spine plasticity and presents a catalogue of candidate 'LTP miRNAs'.

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References
1.
Hofer S, Mrsic-Flogel T, Bonhoeffer T, Hubener M . Experience leaves a lasting structural trace in cortical circuits. Nature. 2008; 457(7227):313-7. PMC: 6485433. DOI: 10.1038/nature07487. View

2.
Song C, Detert J, Sehgal M, Moyer Jr J . Trace fear conditioning enhances synaptic and intrinsic plasticity in rat hippocampus. J Neurophysiol. 2012; 107(12):3397-408. DOI: 10.1152/jn.00692.2011. View

3.
Malenka R, Bear M . LTP and LTD: an embarrassment of riches. Neuron. 2004; 44(1):5-21. DOI: 10.1016/j.neuron.2004.09.012. View

4.
Phillips R, LeDoux J . Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. Behav Neurosci. 1992; 106(2):274-85. DOI: 10.1037//0735-7044.106.2.274. View

5.
Maren S, Fanselow M . Electrolytic lesions of the fimbria/fornix, dorsal hippocampus, or entorhinal cortex produce anterograde deficits in contextual fear conditioning in rats. Neurobiol Learn Mem. 1997; 67(2):142-9. DOI: 10.1006/nlme.1996.3752. View