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Regulation of behavioral response to stress by microRNA-690

Psychiatric disorders are affected by genetic susceptibility and environmental adversities. Therefore, the regulation of gene expression under certain environments, such as stress, is a key issue in psychiatric disorders. MicroRNAs (miRNAs) have been implicated as post-transcriptional regulators of...

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Autores principales: Park, Jungyoung, Lee, Joonhee, Choi, Koeul, Kang, Hyo Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797085/
https://www.ncbi.nlm.nih.gov/pubmed/33422095
http://dx.doi.org/10.1186/s13041-021-00728-3
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author Park, Jungyoung
Lee, Joonhee
Choi, Koeul
Kang, Hyo Jung
author_facet Park, Jungyoung
Lee, Joonhee
Choi, Koeul
Kang, Hyo Jung
author_sort Park, Jungyoung
collection PubMed
description Psychiatric disorders are affected by genetic susceptibility and environmental adversities. Therefore, the regulation of gene expression under certain environments, such as stress, is a key issue in psychiatric disorders. MicroRNAs (miRNAs) have been implicated as post-transcriptional regulators of several biological processes, which can be differentially controlled through the targeting of multiple mRNAs. However, studies reporting the functions of miRNAs in relation to stress are lacking. In this study, we identified a significant increase in the expression of miRNA-690 (miR-690) in the medial prefrontal cortex (mPFC) of FK506-binding protein 51 knock-out (Fkbp5 KO) mice. In addition, the expression pattern of miR-690 was similar to the sucrose preference of the same group in WT and Fkbp5 KO mice. miR-690 was injected into the mPFC using a recombinant adeno-associated virus mediated gene delivery method. After recovery, miR-690 overexpressing mice were exposed to restraint stress for 2 weeks. In the sucrose preference test and forced swim test, the stressed miR-690 overexpressing mice showed higher sucrose preference and lower immobility time, respectively, than stressed mice injected with the control virus. In the novel object recognition test, the stressed miR-690 overexpressing mice interacted longer with the novel object than those injected with the control virus. These results showed that miR-690 might play a role in stress resilience and could provide new insights into the epigenetic regulation of stress-associated biological functions and diseases, such as depression and post-traumatic stress disorder.
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spelling pubmed-77970852021-01-11 Regulation of behavioral response to stress by microRNA-690 Park, Jungyoung Lee, Joonhee Choi, Koeul Kang, Hyo Jung Mol Brain Micro Report Psychiatric disorders are affected by genetic susceptibility and environmental adversities. Therefore, the regulation of gene expression under certain environments, such as stress, is a key issue in psychiatric disorders. MicroRNAs (miRNAs) have been implicated as post-transcriptional regulators of several biological processes, which can be differentially controlled through the targeting of multiple mRNAs. However, studies reporting the functions of miRNAs in relation to stress are lacking. In this study, we identified a significant increase in the expression of miRNA-690 (miR-690) in the medial prefrontal cortex (mPFC) of FK506-binding protein 51 knock-out (Fkbp5 KO) mice. In addition, the expression pattern of miR-690 was similar to the sucrose preference of the same group in WT and Fkbp5 KO mice. miR-690 was injected into the mPFC using a recombinant adeno-associated virus mediated gene delivery method. After recovery, miR-690 overexpressing mice were exposed to restraint stress for 2 weeks. In the sucrose preference test and forced swim test, the stressed miR-690 overexpressing mice showed higher sucrose preference and lower immobility time, respectively, than stressed mice injected with the control virus. In the novel object recognition test, the stressed miR-690 overexpressing mice interacted longer with the novel object than those injected with the control virus. These results showed that miR-690 might play a role in stress resilience and could provide new insights into the epigenetic regulation of stress-associated biological functions and diseases, such as depression and post-traumatic stress disorder. BioMed Central 2021-01-09 /pmc/articles/PMC7797085/ /pubmed/33422095 http://dx.doi.org/10.1186/s13041-021-00728-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Micro Report
Park, Jungyoung
Lee, Joonhee
Choi, Koeul
Kang, Hyo Jung
Regulation of behavioral response to stress by microRNA-690
title Regulation of behavioral response to stress by microRNA-690
title_full Regulation of behavioral response to stress by microRNA-690
title_fullStr Regulation of behavioral response to stress by microRNA-690
title_full_unstemmed Regulation of behavioral response to stress by microRNA-690
title_short Regulation of behavioral response to stress by microRNA-690
title_sort regulation of behavioral response to stress by microrna-690
topic Micro Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797085/
https://www.ncbi.nlm.nih.gov/pubmed/33422095
http://dx.doi.org/10.1186/s13041-021-00728-3
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