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Increased hippocampal excitability in miR-324-null mice

Authors :
Michael D. Briggs
Robert M. Jackson
Dimitra Tsompani
Yao Hao
Katarzyna A. Piróg
Tamara Modebadze
Jamie Soul
Gavin J. Clowry
David Young
Fiona E. N. LeBeau
Sarah Charlton
Colin G. Miles
Ian M. Clark
Dan J. Hayman
Kathleen Cheung
Hua Lin
Matt J. Barter
Source :
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021), Scientific Reports
Publication Year :
2021

Abstract

MicroRNAs are non-coding RNAs that act to downregulate the expression of target genes by translational repression and degradation of messenger RNA molecules. Individual microRNAs have the ability to specifically target a wide array of gene transcripts, therefore allowing each microRNA to play key roles in multiple biological pathways. miR-324 is a microRNA predicted to target thousands of RNA transcripts and is expressed far more highly in the brain than in any other tissue, suggesting that it may play a role in one or multiple neurological pathways. Here we present data from the first global miR-324-null mice, in which increased excitability and interictal discharges were identified in vitro in the hippocampus. RNA sequencing was used to identify differentially expressed genes in miR-324-null mice which may contribute to this increased hippocampal excitability, and 3′UTR luciferase assays and western blotting revealed that two of these, Suox and Cd300lf, are novel direct targets of miR-324. Characterisation of microRNAs that produce an effect on neurological activity, such as miR-324, and identification of the pathways they regulate will allow a better understanding of the processes involved in normal neurological function and in turn may present novel pharmaceutical targets in treating neurological disease.

Details

Language :
English
Database :
OpenAIRE
Journal :
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021), Scientific Reports
Accession number :
edsair.doi.dedup.....d418215007155d56e894db76e03d3933