RNA-seq characterization of spinal cord injury transcriptome in acute/subacute phases: a resource for understanding the pathology at the systems level
Spinal cord injury (SCI) is a devastating neurological disease without effective treatment. To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI...
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description | Spinal cord injury (SCI) is a devastating neurological disease without effective treatment. To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI in mice. We sequenced tissue samples from acute and subacute phases (2 days and 7 days after injury) and systematically characterized the transcriptomes with the goal of identifying pathways and genes critical in SCI pathology. The top enriched functional categories include "inflammation response," "neurological disease," "cell death and survival" and "nervous system development." The top enriched pathways include LXR/RXR Activation and Atherosclerosis Signaling, etc. Furthermore, we developed a systems-based analysis framework in order to identify key determinants in the global gene networks of the acute and sub-acute phases. Some candidate genes that we identified have been shown to play important roles in SCI, which demonstrates the validity of our approach. There are also many genes whose functions in SCI have not been well studied and can be further investigated by future experiments. We have also incorporated pharmacogenomic information into our analyses. Among the genes identified, the ones with existing drug information can be readily tested in SCI animal models. Therefore, in this study we have described an example of how global gene profiling can be translated to identifying genes of interest for functional tests in the future and generating new hypotheses. Additionally, the RNA-Seq enables splicing isoform identification and the estimation of expression levels, thus providing useful information for increasing the specificity of drug design and reducing potential side effect. In summary, these results provide a valuable reference data resource for a better understanding of the SCI process in the acute and sub-acute phases. |
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To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI in mice. We sequenced tissue samples from acute and subacute phases (2 days and 7 days after injury) and systematically characterized the transcriptomes with the goal of identifying pathways and genes critical in SCI pathology. The top enriched functional categories include "inflammation response," "neurological disease," "cell death and survival" and "nervous system development." The top enriched pathways include LXR/RXR Activation and Atherosclerosis Signaling, etc. Furthermore, we developed a systems-based analysis framework in order to identify key determinants in the global gene networks of the acute and sub-acute phases. Some candidate genes that we identified have been shown to play important roles in SCI, which demonstrates the validity of our approach. There are also many genes whose functions in SCI have not been well studied and can be further investigated by future experiments. We have also incorporated pharmacogenomic information into our analyses. Among the genes identified, the ones with existing drug information can be readily tested in SCI animal models. Therefore, in this study we have described an example of how global gene profiling can be translated to identifying genes of interest for functional tests in the future and generating new hypotheses. Additionally, the RNA-Seq enables splicing isoform identification and the estimation of expression levels, thus providing useful information for increasing the specificity of drug design and reducing potential side effect. In summary, these results provide a valuable reference data resource for a better understanding of the SCI process in the acute and sub-acute phases.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0072567</identifier><identifier>PMID: 23951329</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal models ; Animals ; Arteriosclerosis ; Atherosclerosis ; Cell death ; Cell survival ; Drug development ; Female ; Gene Expression ; Gene Expression Profiling ; Gene Regulatory Networks ; Gene sequencing ; Genes ; Inflammation - genetics ; Inflammation - metabolism ; Inflammation - pathology ; Injuries ; Laboratory animals ; Lipids ; Lipoproteins ; Medical schools ; Medical treatment ; Medicine ; Metabolism ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Annotation ; Nervous system ; Nervous system diseases ; Neurosurgery ; Oligonucleotide Array Sequence Analysis ; Pathology ; Pharmacogenomics ; Pharmacology ; Phases ; Retinoid X receptors ; Ribonucleic acid ; RNA ; RNA Isoforms - genetics ; RNA Isoforms - metabolism ; RNA sequencing ; RNA Splicing ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Rodents ; Sequence Analysis, RNA ; Side effects ; Signaling ; Spinal cord injuries ; Spinal Cord Injuries - genetics ; Spinal Cord Injuries - metabolism ; Spinal Cord Injuries - pathology ; Splicing ; Stem cells ; Studies ; Transcriptome</subject><ispartof>PloS one, 2013-08, Vol.8 (8), p.e72567-e72567</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Chen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Chen et al 2013 Chen et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-1b2e5af3609cf531ba02f696342a09f123cb69dfaaf8f8ab2ea154ae4851e3003</citedby><cites>FETCH-LOGICAL-c692t-1b2e5af3609cf531ba02f696342a09f123cb69dfaaf8f8ab2ea154ae4851e3003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739761/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739761/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23951329$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hetman, Michal</contributor><creatorcontrib>Chen, Kenian</creatorcontrib><creatorcontrib>Deng, Shuyun</creatorcontrib><creatorcontrib>Lu, Hezuo</creatorcontrib><creatorcontrib>Zheng, Yiyan</creatorcontrib><creatorcontrib>Yang, Guodong</creatorcontrib><creatorcontrib>Kim, Dong</creatorcontrib><creatorcontrib>Cao, Qilin</creatorcontrib><creatorcontrib>Wu, Jia Qian</creatorcontrib><title>RNA-seq characterization of spinal cord injury transcriptome in acute/subacute phases: a resource for understanding the pathology at the systems level</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Spinal cord injury (SCI) is a devastating neurological disease without effective treatment. To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI in mice. We sequenced tissue samples from acute and subacute phases (2 days and 7 days after injury) and systematically characterized the transcriptomes with the goal of identifying pathways and genes critical in SCI pathology. The top enriched functional categories include "inflammation response," "neurological disease," "cell death and survival" and "nervous system development." The top enriched pathways include LXR/RXR Activation and Atherosclerosis Signaling, etc. Furthermore, we developed a systems-based analysis framework in order to identify key determinants in the global gene networks of the acute and sub-acute phases. Some candidate genes that we identified have been shown to play important roles in SCI, which demonstrates the validity of our approach. There are also many genes whose functions in SCI have not been well studied and can be further investigated by future experiments. We have also incorporated pharmacogenomic information into our analyses. Among the genes identified, the ones with existing drug information can be readily tested in SCI animal models. Therefore, in this study we have described an example of how global gene profiling can be translated to identifying genes of interest for functional tests in the future and generating new hypotheses. Additionally, the RNA-Seq enables splicing isoform identification and the estimation of expression levels, thus providing useful information for increasing the specificity of drug design and reducing potential side effect. In summary, these results provide a valuable reference data resource for a better understanding of the SCI process in the acute and sub-acute phases.</description><subject>Animal models</subject><subject>Animals</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Cell death</subject><subject>Cell survival</subject><subject>Drug development</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Regulatory Networks</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Inflammation - genetics</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - pathology</subject><subject>Injuries</subject><subject>Laboratory animals</subject><subject>Lipids</subject><subject>Lipoproteins</subject><subject>Medical schools</subject><subject>Medical treatment</subject><subject>Medicine</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Molecular Sequence Annotation</subject><subject>Nervous system</subject><subject>Nervous system diseases</subject><subject>Neurosurgery</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Pathology</subject><subject>Pharmacogenomics</subject><subject>Pharmacology</subject><subject>Phases</subject><subject>Retinoid X receptors</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA Isoforms - genetics</subject><subject>RNA Isoforms - metabolism</subject><subject>RNA sequencing</subject><subject>RNA Splicing</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Sequence Analysis, RNA</subject><subject>Side effects</subject><subject>Signaling</subject><subject>Spinal cord injuries</subject><subject>Spinal Cord Injuries - genetics</subject><subject>Spinal Cord Injuries - metabolism</subject><subject>Spinal Cord Injuries - pathology</subject><subject>Splicing</subject><subject>Stem cells</subject><subject>Studies</subject><subject>Transcriptome</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9tq3DAQhk1padK0b1BaQaG0F7uRLFu2c1FYQg8LoYH0cCvG8mitxWttJDl0-yB93moPCXHJRdGFxOibf6RfmiR5yeiU8YKdLu3geuima9vjlNIizUXxKDlmFU8nIqX88b31UfLM-yWlOS-FeJocpbzKGU-r4-TP1dfZxOM1US04UAGd-Q3B2J5YTfzaxApEWdcQ0y8HtyHBQe-VM-tgVxiDBNQQ8NQP9W5B1i149GcEiEMfT6iQaOvI0DfofIC-Mf2ChDaCEFrb2cWGQNgF_MYHXHnS4Q12z5MnGjqPLw7zSfLj08fv518mF5ef5-ezi4kSVRomrE4xB80FrZTOOauBplpUgmcp0EqzlKtaVI0G0KUuIdLA8gwwK3OGnFJ-krze66476-XBUi9ZxmlRRrvySMz3RGNhKdfOrMBtpAUjdwHrFhJcMKpDmYmshEKhVopnlOqqLqqmyHmjdKG0VlHrw6HaUK-wUdhHO7uR6HinN61c2BvJC14VgkWBdwcBZ68H9EGujFfYddCjHbbnTgWNry6qiL75B334dgdqAfECptc21lVbUTnLipKLaOGWmj5AxdHgyqj4_7SJ8VHC-1FCZAL-CgsYvJfzb1f_z17-HLNv77EtQhdab7th-2H9GMz2oHLWe4f6zmRG5bZ9bt2Q2_aRh_aJaa_uP9Bd0m2_8L_uxxkA</recordid><startdate>20130809</startdate><enddate>20130809</enddate><creator>Chen, Kenian</creator><creator>Deng, Shuyun</creator><creator>Lu, Hezuo</creator><creator>Zheng, Yiyan</creator><creator>Yang, Guodong</creator><creator>Kim, Dong</creator><creator>Cao, Qilin</creator><creator>Wu, Jia Qian</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130809</creationdate><title>RNA-seq characterization of spinal cord injury transcriptome in acute/subacute phases: a resource for understanding the pathology at the systems level</title><author>Chen, Kenian ; Deng, Shuyun ; Lu, Hezuo ; Zheng, Yiyan ; Yang, Guodong ; Kim, Dong ; Cao, Qilin ; Wu, Jia Qian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-1b2e5af3609cf531ba02f696342a09f123cb69dfaaf8f8ab2ea154ae4851e3003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Cell death</topic><topic>Cell survival</topic><topic>Drug development</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Gene Expression Profiling</topic><topic>Gene Regulatory Networks</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Inflammation - 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To generate a comprehensive view of the mechanisms involved in SCI pathology, we applied RNA-Sequencing (RNA-Seq) technology to characterize the temporal changes in global gene expression after contusive SCI in mice. We sequenced tissue samples from acute and subacute phases (2 days and 7 days after injury) and systematically characterized the transcriptomes with the goal of identifying pathways and genes critical in SCI pathology. The top enriched functional categories include "inflammation response," "neurological disease," "cell death and survival" and "nervous system development." The top enriched pathways include LXR/RXR Activation and Atherosclerosis Signaling, etc. Furthermore, we developed a systems-based analysis framework in order to identify key determinants in the global gene networks of the acute and sub-acute phases. Some candidate genes that we identified have been shown to play important roles in SCI, which demonstrates the validity of our approach. There are also many genes whose functions in SCI have not been well studied and can be further investigated by future experiments. We have also incorporated pharmacogenomic information into our analyses. Among the genes identified, the ones with existing drug information can be readily tested in SCI animal models. Therefore, in this study we have described an example of how global gene profiling can be translated to identifying genes of interest for functional tests in the future and generating new hypotheses. Additionally, the RNA-Seq enables splicing isoform identification and the estimation of expression levels, thus providing useful information for increasing the specificity of drug design and reducing potential side effect. In summary, these results provide a valuable reference data resource for a better understanding of the SCI process in the acute and sub-acute phases.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23951329</pmid><doi>10.1371/journal.pone.0072567</doi><tpages>e72567</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Animal models Animals Arteriosclerosis Atherosclerosis Cell death Cell survival Drug development Female Gene Expression Gene Expression Profiling Gene Regulatory Networks Gene sequencing Genes Inflammation - genetics Inflammation - metabolism Inflammation - pathology Injuries Laboratory animals Lipids Lipoproteins Medical schools Medical treatment Medicine Metabolism Mice Mice, Inbred C57BL Molecular Sequence Annotation Nervous system Nervous system diseases Neurosurgery Oligonucleotide Array Sequence Analysis Pathology Pharmacogenomics Pharmacology Phases Retinoid X receptors Ribonucleic acid RNA RNA Isoforms - genetics RNA Isoforms - metabolism RNA sequencing RNA Splicing RNA, Messenger - genetics RNA, Messenger - metabolism Rodents Sequence Analysis, RNA Side effects Signaling Spinal cord injuries Spinal Cord Injuries - genetics Spinal Cord Injuries - metabolism Spinal Cord Injuries - pathology Splicing Stem cells Studies Transcriptome |
title | RNA-seq characterization of spinal cord injury transcriptome in acute/subacute phases: a resource for understanding the pathology at the systems level |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T10%3A18%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=RNA-seq%20characterization%20of%20spinal%20cord%20injury%20transcriptome%20in%20acute/subacute%20phases:%20a%20resource%20for%20understanding%20the%20pathology%20at%20the%20systems%20level&rft.jtitle=PloS%20one&rft.au=Chen,%20Kenian&rft.date=2013-08-09&rft.volume=8&rft.issue=8&rft.spage=e72567&rft.epage=e72567&rft.pages=e72567-e72567&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0072567&rft_dat=%3Cgale_plos_%3EA478361235%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1430780535&rft_id=info:pmid/23951329&rft_galeid=A478361235&rft_doaj_id=oai_doaj_org_article_4648a7cefcc3400f9b79d753dcf7cffc&rfr_iscdi=true |