Transcriptome analysis of long non-coding RNAs of the nucleus accumbens in cocaine-conditioned mice

Cocaine dependence involves in the brain's reward circuit as well as nucleus accumbens (NAc), a key region of the mesolimbic dopamine pathway. Many studies have documented altered expression of genes and identified transcription factor networks and epigenetic processes that are fundamental to c...

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Veröffentlicht in:Journal of neurochemistry 2012-12, Vol.123 (5), p.790-799
Hauptverfasser: Bu, Qian, Hu, Zhengtao, Chen, Feng, Zhu, Ruiming, Deng, Yi, Shao, Xue, Li, Yan, Zhao, Jinxuan, Li, Hongyu, Zhang, Baolai, Lv, Lei, Yan, Guangyan, Zhao, Yinglan, Cen, Xiaobo
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container_issue 5
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container_title Journal of neurochemistry
container_volume 123
creator Bu, Qian
Hu, Zhengtao
Chen, Feng
Zhu, Ruiming
Deng, Yi
Shao, Xue
Li, Yan
Zhao, Jinxuan
Li, Hongyu
Zhang, Baolai
Lv, Lei
Yan, Guangyan
Zhao, Yinglan
Cen, Xiaobo
description Cocaine dependence involves in the brain's reward circuit as well as nucleus accumbens (NAc), a key region of the mesolimbic dopamine pathway. Many studies have documented altered expression of genes and identified transcription factor networks and epigenetic processes that are fundamental to cocaine addiction. However, all these investigations have focused on mRNA of encoding genes, which may not always reflect the involvement of long non‐coding RNAs (lncRNAs), which has been implied in a broad range of biological processes and complex diseases including brain development and neuropathological process. To explore the potential involvement of lncRNAs in drug addiction, which is viewed as a form of aberrant neuroplasticity, we used a custom‐designed microarray to examine the expression profiles of mRNAs and lncRNAs in brain NAc of cocaine‐conditioned mice and identified 764 mRNAs, and 603 lncRNAs were differentially expressed. Candidate lncRNAs were identified for further genomic context characterization as sense‐overlap, antisense‐overlap, intergenic, bidirection, and ultra‐conserved region encoding lncRNAs. We found that 410 candidate lncRNAs which have been reported to act in cis or trans to their targeted loci, providing 48 pair mRNA‐lncRNAs. These results suggest that the modification of mRNAs expression by cocaine may be associated with the actions of lncRNAs. Taken together, our results show that cocaine can cause the genome‐wide alterations of lncRNAs expressed in NAc, and some of these modified RNA transcripts may to play a role in cocaine‐induced neural plasticity and addiction. Cocaine Modifies Transcriptional Profiling of lncRNAs LncRNAhas been shown to be involved in various neurological diseases;however, itsrole in drug addiction is unknown. Here, we identified 603 lncRNAs changed significantly in brain nucleus accunbens of cocaine‐dependent mice, providing 48 pair mRNA‐lncRNAs significantly modified. These findings provide for the first time new insights intothepotentialinvolvement of lncRNAs in neuroplasticity and drug addiction.
doi_str_mv 10.1111/jnc.12006
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Many studies have documented altered expression of genes and identified transcription factor networks and epigenetic processes that are fundamental to cocaine addiction. However, all these investigations have focused on mRNA of encoding genes, which may not always reflect the involvement of long non‐coding RNAs (lncRNAs), which has been implied in a broad range of biological processes and complex diseases including brain development and neuropathological process. To explore the potential involvement of lncRNAs in drug addiction, which is viewed as a form of aberrant neuroplasticity, we used a custom‐designed microarray to examine the expression profiles of mRNAs and lncRNAs in brain NAc of cocaine‐conditioned mice and identified 764 mRNAs, and 603 lncRNAs were differentially expressed. Candidate lncRNAs were identified for further genomic context characterization as sense‐overlap, antisense‐overlap, intergenic, bidirection, and ultra‐conserved region encoding lncRNAs. We found that 410 candidate lncRNAs which have been reported to act in cis or trans to their targeted loci, providing 48 pair mRNA‐lncRNAs. These results suggest that the modification of mRNAs expression by cocaine may be associated with the actions of lncRNAs. Taken together, our results show that cocaine can cause the genome‐wide alterations of lncRNAs expressed in NAc, and some of these modified RNA transcripts may to play a role in cocaine‐induced neural plasticity and addiction. Cocaine Modifies Transcriptional Profiling of lncRNAs LncRNAhas been shown to be involved in various neurological diseases;however, itsrole in drug addiction is unknown. Here, we identified 603 lncRNAs changed significantly in brain nucleus accunbens of cocaine‐dependent mice, providing 48 pair mRNA‐lncRNAs significantly modified. These findings provide for the first time new insights intothepotentialinvolvement of lncRNAs in neuroplasticity and drug addiction.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/jnc.12006</identifier><identifier>PMID: 22957495</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Addictive behaviors ; Adult and adolescent clinical studies ; Animals ; Biological and medical sciences ; Brain ; Brain diseases ; Circuits ; Cocaine ; Cocaine-Related Disorders - genetics ; Conditioning, Operant ; DNA microarrays ; Dopamine ; Drug addiction ; Drug addictions ; Epigenetics ; Gene expression ; genomics ; lncRNA ; Male ; Medical sciences ; Mesolimbic system ; Mice ; Mice, Inbred C57BL ; Neurochemistry ; non-coding RNA ; Nucleus Accumbens ; Plasticity ; Plasticity (neural) ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Real-Time Polymerase Chain Reaction ; Reinforcement ; RNA, Untranslated - analysis ; RNA, Untranslated - genetics ; Toxicology ; Transcription factors ; Transcriptome</subject><ispartof>Journal of neurochemistry, 2012-12, Vol.123 (5), p.790-799</ispartof><rights>2012 The Authors Journal of Neurochemistry © 2012 International Society for Neurochemistry</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors Journal of Neurochemistry © 2012 International Society for Neurochemistry.</rights><rights>2012 International Society for Neurochemistry</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjnc.12006$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjnc.12006$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26700973$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22957495$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bu, Qian</creatorcontrib><creatorcontrib>Hu, Zhengtao</creatorcontrib><creatorcontrib>Chen, Feng</creatorcontrib><creatorcontrib>Zhu, Ruiming</creatorcontrib><creatorcontrib>Deng, Yi</creatorcontrib><creatorcontrib>Shao, Xue</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Zhao, Jinxuan</creatorcontrib><creatorcontrib>Li, Hongyu</creatorcontrib><creatorcontrib>Zhang, Baolai</creatorcontrib><creatorcontrib>Lv, Lei</creatorcontrib><creatorcontrib>Yan, Guangyan</creatorcontrib><creatorcontrib>Zhao, Yinglan</creatorcontrib><creatorcontrib>Cen, Xiaobo</creatorcontrib><title>Transcriptome analysis of long non-coding RNAs of the nucleus accumbens in cocaine-conditioned mice</title><title>Journal of neurochemistry</title><addtitle>J. Neurochem</addtitle><description>Cocaine dependence involves in the brain's reward circuit as well as nucleus accumbens (NAc), a key region of the mesolimbic dopamine pathway. Many studies have documented altered expression of genes and identified transcription factor networks and epigenetic processes that are fundamental to cocaine addiction. However, all these investigations have focused on mRNA of encoding genes, which may not always reflect the involvement of long non‐coding RNAs (lncRNAs), which has been implied in a broad range of biological processes and complex diseases including brain development and neuropathological process. To explore the potential involvement of lncRNAs in drug addiction, which is viewed as a form of aberrant neuroplasticity, we used a custom‐designed microarray to examine the expression profiles of mRNAs and lncRNAs in brain NAc of cocaine‐conditioned mice and identified 764 mRNAs, and 603 lncRNAs were differentially expressed. Candidate lncRNAs were identified for further genomic context characterization as sense‐overlap, antisense‐overlap, intergenic, bidirection, and ultra‐conserved region encoding lncRNAs. We found that 410 candidate lncRNAs which have been reported to act in cis or trans to their targeted loci, providing 48 pair mRNA‐lncRNAs. These results suggest that the modification of mRNAs expression by cocaine may be associated with the actions of lncRNAs. Taken together, our results show that cocaine can cause the genome‐wide alterations of lncRNAs expressed in NAc, and some of these modified RNA transcripts may to play a role in cocaine‐induced neural plasticity and addiction. Cocaine Modifies Transcriptional Profiling of lncRNAs LncRNAhas been shown to be involved in various neurological diseases;however, itsrole in drug addiction is unknown. Here, we identified 603 lncRNAs changed significantly in brain nucleus accunbens of cocaine‐dependent mice, providing 48 pair mRNA‐lncRNAs significantly modified. 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Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reinforcement</topic><topic>RNA, Untranslated - analysis</topic><topic>RNA, Untranslated - genetics</topic><topic>Toxicology</topic><topic>Transcription factors</topic><topic>Transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bu, Qian</creatorcontrib><creatorcontrib>Hu, Zhengtao</creatorcontrib><creatorcontrib>Chen, Feng</creatorcontrib><creatorcontrib>Zhu, Ruiming</creatorcontrib><creatorcontrib>Deng, Yi</creatorcontrib><creatorcontrib>Shao, Xue</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><creatorcontrib>Zhao, Jinxuan</creatorcontrib><creatorcontrib>Li, Hongyu</creatorcontrib><creatorcontrib>Zhang, Baolai</creatorcontrib><creatorcontrib>Lv, Lei</creatorcontrib><creatorcontrib>Yan, Guangyan</creatorcontrib><creatorcontrib>Zhao, Yinglan</creatorcontrib><creatorcontrib>Cen, Xiaobo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bu, Qian</au><au>Hu, Zhengtao</au><au>Chen, Feng</au><au>Zhu, Ruiming</au><au>Deng, Yi</au><au>Shao, Xue</au><au>Li, Yan</au><au>Zhao, Jinxuan</au><au>Li, Hongyu</au><au>Zhang, Baolai</au><au>Lv, Lei</au><au>Yan, Guangyan</au><au>Zhao, Yinglan</au><au>Cen, Xiaobo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptome analysis of long non-coding RNAs of the nucleus accumbens in cocaine-conditioned mice</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J. Neurochem</addtitle><date>2012-12</date><risdate>2012</risdate><volume>123</volume><issue>5</issue><spage>790</spage><epage>799</epage><pages>790-799</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>Cocaine dependence involves in the brain's reward circuit as well as nucleus accumbens (NAc), a key region of the mesolimbic dopamine pathway. Many studies have documented altered expression of genes and identified transcription factor networks and epigenetic processes that are fundamental to cocaine addiction. However, all these investigations have focused on mRNA of encoding genes, which may not always reflect the involvement of long non‐coding RNAs (lncRNAs), which has been implied in a broad range of biological processes and complex diseases including brain development and neuropathological process. To explore the potential involvement of lncRNAs in drug addiction, which is viewed as a form of aberrant neuroplasticity, we used a custom‐designed microarray to examine the expression profiles of mRNAs and lncRNAs in brain NAc of cocaine‐conditioned mice and identified 764 mRNAs, and 603 lncRNAs were differentially expressed. Candidate lncRNAs were identified for further genomic context characterization as sense‐overlap, antisense‐overlap, intergenic, bidirection, and ultra‐conserved region encoding lncRNAs. We found that 410 candidate lncRNAs which have been reported to act in cis or trans to their targeted loci, providing 48 pair mRNA‐lncRNAs. These results suggest that the modification of mRNAs expression by cocaine may be associated with the actions of lncRNAs. Taken together, our results show that cocaine can cause the genome‐wide alterations of lncRNAs expressed in NAc, and some of these modified RNA transcripts may to play a role in cocaine‐induced neural plasticity and addiction. Cocaine Modifies Transcriptional Profiling of lncRNAs LncRNAhas been shown to be involved in various neurological diseases;however, itsrole in drug addiction is unknown. Here, we identified 603 lncRNAs changed significantly in brain nucleus accunbens of cocaine‐dependent mice, providing 48 pair mRNA‐lncRNAs significantly modified. These findings provide for the first time new insights intothepotentialinvolvement of lncRNAs in neuroplasticity and drug addiction.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>22957495</pmid><doi>10.1111/jnc.12006</doi><tpages>10</tpages></addata></record>
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subjects Addictive behaviors
Adult and adolescent clinical studies
Animals
Biological and medical sciences
Brain
Brain diseases
Circuits
Cocaine
Cocaine-Related Disorders - genetics
Conditioning, Operant
DNA microarrays
Dopamine
Drug addiction
Drug addictions
Epigenetics
Gene expression
genomics
lncRNA
Male
Medical sciences
Mesolimbic system
Mice
Mice, Inbred C57BL
Neurochemistry
non-coding RNA
Nucleus Accumbens
Plasticity
Plasticity (neural)
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Real-Time Polymerase Chain Reaction
Reinforcement
RNA, Untranslated - analysis
RNA, Untranslated - genetics
Toxicology
Transcription factors
Transcriptome
title Transcriptome analysis of long non-coding RNAs of the nucleus accumbens in cocaine-conditioned mice
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