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The Brain-Enriched MicroRNA miR-9-3p Regulates Synaptic Plasticity and Memory

Authors
Sim, Su-EonLim, Chae-SeokKim, Jae-IckSeo, DaekwanChun, HeejungYu, Nam-KyungLee, JaehyunKang, SukJae JoshuaKo, Hyoung-GonChoi, Jun-HyeokKim, TaehyunJang, Eun-HaeHan, JoohyunBak, Myeong SeongPark, Jong-EunJang, Deok-JinBaek, DaehyunLee, Yong-SeokKaang, Bong-Kiun
Issue Date
Aug-2016
Publisher
SOC NEUROSCIENCE
Keywords
hippocampus; long-term potentiation; memory; microRNA
Citation
JOURNAL OF NEUROSCIENCE, v.36, no.33, pp 8641 - 8652
Pages
12
Journal Title
JOURNAL OF NEUROSCIENCE
Volume
36
Number
33
Start Page
8641
End Page
8652
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/64194
DOI
10.1523/JNEUROSCI.0630-16.2016
ISSN
0270-6474
1529-2401
Abstract
MicroRNAs (miRNAs) are small, noncoding RNAs that posttranscriptionally regulate gene expression in many tissues. Although a number of brain-enriched miRNAs have been identified, only a few specific miRNAs have been revealed as critical regulators of synaptic plasticity, learning, and memory. miR-9-5p/3p are brain-enriched miRNAs known to regulate development and their changes have been implicated in several neurological disorders, yet their role in mature neurons in mice is largely unknown. Here, we report that inhibition of miR-9-3p, but not miR-9-5p, impaired hippocampal long-term potentiation (LTP) without affecting basal synaptic transmission. Moreover, inhibition of miR-9-3p in the hippocampus resulted in learning and memory deficits. Furthermore, miR-9-3p inhibition increased the expression of the LTP-related genes Dmd and SAP97, the expression levels of which are negatively correlated with LTP. These results suggest that miR-9-3p-mediated gene regulation plays important roles in synaptic plasticity and hippocampus-dependent memory.
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