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Fear extinction is regulated by the activity of long noncoding RNAs at the synapse
Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory for...
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Published in: | Nature communications 2023-11, Vol.14 (1), p.7616-7616, Article 7616 |
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creator | Liau, Wei-Siang Zhao, Qiongyi Bademosi, Adekunle Gormal, Rachel S. Gong, Hao Marshall, Paul R. Periyakaruppiah, Ambika Madugalle, Sachithrani U. Zajaczkowski, Esmi L. Leighton, Laura J. Ren, Haobin Musgrove, Mason Davies, Joshua Rauch, Simone He, Chuan Dickinson, Bryan C. Li, Xiang Wei, Wei Meunier, Frédéric A. Fernández-Moya, Sandra M. Kiebler, Michael A. Srinivasan, Balakumar Banerjee, Sourav Clark, Michael Spitale, Robert C. Bredy, Timothy W. |
description | Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA,
Gas5
. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this
Gas5
isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the
Gas5
variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.
Synaptic activity controls the extinction of conditioned fear. Here the authors discovered a new way that the brain controls memories of fear: a long noncoding RNA called Gas5 that coordinates the activity of RNA granules in the synaptic compartment. |
doi_str_mv | 10.1038/s41467-023-43535-1 |
format | article |
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Gas5
. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this
Gas5
isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the
Gas5
variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.
Synaptic activity controls the extinction of conditioned fear. Here the authors discovered a new way that the brain controls memories of fear: a long noncoding RNA called Gas5 that coordinates the activity of RNA granules in the synaptic compartment.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-023-43535-1</identifier><identifier>PMID: 37993455</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14/19 ; 38/90 ; 38/91 ; 631/208/200 ; 631/337/384/2568 ; 631/378/1595 ; 631/378/340 ; Alternative splicing ; Animals ; Brain ; Brain research ; Clustering ; Extinction (Learning) ; Extinction behavior ; Extinction, Psychological ; Fear ; Fear conditioning ; Granular materials ; Humanities and Social Sciences ; Immunoprecipitation ; Male ; Mass spectrometry ; Mass spectroscopy ; Memory ; Mice ; multidisciplinary ; Neuroimaging ; Non-coding RNA ; Prefrontal cortex ; Prefrontal Cortex - metabolism ; Regenerative medicine ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; RNA-binding protein ; Science ; Science (multidisciplinary) ; Synapses ; Synapses - metabolism</subject><ispartof>Nature communications, 2023-11, Vol.14 (1), p.7616-7616, Article 7616</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA,
Gas5
. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this
Gas5
isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the
Gas5
variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.
Synaptic activity controls the extinction of conditioned fear. Here the authors discovered a new way that the brain controls memories of fear: a long noncoding RNA called Gas5 that coordinates the activity of RNA granules in the synaptic compartment.</description><subject>14/19</subject><subject>38/90</subject><subject>38/91</subject><subject>631/208/200</subject><subject>631/337/384/2568</subject><subject>631/378/1595</subject><subject>631/378/340</subject><subject>Alternative splicing</subject><subject>Animals</subject><subject>Brain</subject><subject>Brain research</subject><subject>Clustering</subject><subject>Extinction (Learning)</subject><subject>Extinction behavior</subject><subject>Extinction, Psychological</subject><subject>Fear</subject><subject>Fear conditioning</subject><subject>Granular materials</subject><subject>Humanities and Social Sciences</subject><subject>Immunoprecipitation</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Memory</subject><subject>Mice</subject><subject>multidisciplinary</subject><subject>Neuroimaging</subject><subject>Non-coding RNA</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Regenerative medicine</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>RNA-binding protein</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Synapses</subject><subject>Synapses - 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Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liau, Wei-Siang</au><au>Zhao, Qiongyi</au><au>Bademosi, Adekunle</au><au>Gormal, Rachel S.</au><au>Gong, Hao</au><au>Marshall, Paul R.</au><au>Periyakaruppiah, Ambika</au><au>Madugalle, Sachithrani U.</au><au>Zajaczkowski, Esmi L.</au><au>Leighton, Laura J.</au><au>Ren, Haobin</au><au>Musgrove, Mason</au><au>Davies, Joshua</au><au>Rauch, Simone</au><au>He, Chuan</au><au>Dickinson, Bryan C.</au><au>Li, Xiang</au><au>Wei, Wei</au><au>Meunier, Frédéric A.</au><au>Fernández-Moya, Sandra M.</au><au>Kiebler, Michael A.</au><au>Srinivasan, Balakumar</au><au>Banerjee, Sourav</au><au>Clark, Michael</au><au>Spitale, Robert C.</au><au>Bredy, Timothy W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fear extinction is regulated by the activity of long noncoding RNAs at the synapse</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2023-11-22</date><risdate>2023</risdate><volume>14</volume><issue>1</issue><spage>7616</spage><epage>7616</epage><pages>7616-7616</pages><artnum>7616</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA,
Gas5
. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this
Gas5
isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the
Gas5
variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.
Synaptic activity controls the extinction of conditioned fear. Here the authors discovered a new way that the brain controls memories of fear: a long noncoding RNA called Gas5 that coordinates the activity of RNA granules in the synaptic compartment.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37993455</pmid><doi>10.1038/s41467-023-43535-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-3246-6959</orcidid><orcidid>https://orcid.org/0000-0002-6341-0416</orcidid><orcidid>https://orcid.org/0000-0002-8850-6297</orcidid><orcidid>https://orcid.org/0000-0002-5894-4296</orcidid><orcidid>https://orcid.org/0000-0003-2151-5858</orcidid><orcidid>https://orcid.org/0000-0003-0989-7283</orcidid><orcidid>https://orcid.org/0000-0003-0764-7248</orcidid><orcidid>https://orcid.org/0000-0003-3280-126X</orcidid><orcidid>https://orcid.org/0000-0002-3511-8098</orcidid><orcidid>https://orcid.org/0000-0002-2903-9537</orcidid><orcidid>https://orcid.org/0000-0001-8557-6313</orcidid><orcidid>https://orcid.org/0000-0003-4319-7424</orcidid><orcidid>https://orcid.org/0000-0003-1604-0253</orcidid><orcidid>https://orcid.org/0000-0001-8547-4712</orcidid><orcidid>https://orcid.org/0000-0002-9616-1911</orcidid><orcidid>https://orcid.org/0000-0001-5157-8572</orcidid><orcidid>https://orcid.org/0000-0001-6400-1107</orcidid><orcidid>https://orcid.org/0000-0002-3867-5068</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2041-1723 |
ispartof | Nature communications, 2023-11, Vol.14 (1), p.7616-7616, Article 7616 |
issn | 2041-1723 2041-1723 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_988e064ab265447988a0b34da83e4592 |
source | Publicly Available Content Database; Nature; PubMed Central; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 14/19 38/90 38/91 631/208/200 631/337/384/2568 631/378/1595 631/378/340 Alternative splicing Animals Brain Brain research Clustering Extinction (Learning) Extinction behavior Extinction, Psychological Fear Fear conditioning Granular materials Humanities and Social Sciences Immunoprecipitation Male Mass spectrometry Mass spectroscopy Memory Mice multidisciplinary Neuroimaging Non-coding RNA Prefrontal cortex Prefrontal Cortex - metabolism Regenerative medicine RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism RNA-binding protein Science Science (multidisciplinary) Synapses Synapses - metabolism |
title | Fear extinction is regulated by the activity of long noncoding RNAs at the synapse |
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