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A Catalogue of Putative cis-Regulatory Interactions Between Long Non-coding RNAs and Proximal Coding Genes Based on Correlative Analysis Across Diverse Human Tumors
Abstract Antisense transcripts and other long non-coding RNAs are pervasive in mammalian cells, and some of these molecules have been proposed to regulate proximal protein-coding genes in cis. For example, non-coding transcription can contribute to inactivation of tumor suppressor genes in cancer, a...
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Published in: | G3 : genes - genomes - genetics 2018-06, Vol.8 (6), p.2019-2025 |
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description | Abstract
Antisense transcripts and other long non-coding RNAs are pervasive in mammalian cells, and some of these molecules have been proposed to regulate proximal protein-coding genes in cis. For example, non-coding transcription can contribute to inactivation of tumor suppressor genes in cancer, and antisense transcripts have been implicated in the epigenetic inactivation of imprinted genes. However, our knowledge is still limited and more such regulatory interactions likely await discovery. Here, we make use of available gene expression data from a large compendium of human tumors to generate hypotheses regarding non-coding-to-coding cis-regulatory relationships with emphasis on negative associations, as these are less likely to arise for reasons other than cis-regulation. We document a large number of possible regulatory interactions, including 193 coding/non-coding pairs that show expression patterns compatible with negative cis-regulation. Importantly, by this approach we capture several known cases, and many of the involved coding genes have known roles in cancer. Our study provides a large catalog of putative non-coding/coding cis-regulatory pairs that may serve as a basis for further experimental validation and characterization. |
doi_str_mv | 10.1534/g3.118.200296 |
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Antisense transcripts and other long non-coding RNAs are pervasive in mammalian cells, and some of these molecules have been proposed to regulate proximal protein-coding genes in cis. For example, non-coding transcription can contribute to inactivation of tumor suppressor genes in cancer, and antisense transcripts have been implicated in the epigenetic inactivation of imprinted genes. However, our knowledge is still limited and more such regulatory interactions likely await discovery. Here, we make use of available gene expression data from a large compendium of human tumors to generate hypotheses regarding non-coding-to-coding cis-regulatory relationships with emphasis on negative associations, as these are less likely to arise for reasons other than cis-regulation. We document a large number of possible regulatory interactions, including 193 coding/non-coding pairs that show expression patterns compatible with negative cis-regulation. Importantly, by this approach we capture several known cases, and many of the involved coding genes have known roles in cancer. Our study provides a large catalog of putative non-coding/coding cis-regulatory pairs that may serve as a basis for further experimental validation and characterization.</description><identifier>ISSN: 2160-1836</identifier><identifier>EISSN: 2160-1836</identifier><identifier>DOI: 10.1534/g3.118.200296</identifier><identifier>PMID: 29666194</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>cancer ; Cell and Molecular Biology ; Cell- och molekylärbiologi ; chromatin ; correlation ; evolution ; expression ; features ; Genetics & Heredity ; Investigations ; landscape ; lncRNA ; Medical Genetics and Genomics ; Medicinsk genetik och genomik ; neighboring genes ; reveal ; RNAseq ; transcriptome</subject><ispartof>G3 : genes - genomes - genetics, 2018-06, Vol.8 (6), p.2019-2025</ispartof><rights>2018 Basu and Larsson 2018</rights><rights>Copyright © 2018 Basu and Larsson.</rights><rights>Copyright © 2018 Basu and Larsson 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-ae1ad819a51f857c5f2510e9dba3d9ad32212457ed203f424df2dfa1f83ec05c3</citedby><cites>FETCH-LOGICAL-c524t-ae1ad819a51f857c5f2510e9dba3d9ad32212457ed203f424df2dfa1f83ec05c3</cites><orcidid>0000-0003-1400-0119 ; 0000-0001-6107-2487</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982829/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982829/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29666194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/268640$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Basu, Swaraj</creatorcontrib><creatorcontrib>Larsson, Erik</creatorcontrib><title>A Catalogue of Putative cis-Regulatory Interactions Between Long Non-coding RNAs and Proximal Coding Genes Based on Correlative Analysis Across Diverse Human Tumors</title><title>G3 : genes - genomes - genetics</title><addtitle>G3 (Bethesda)</addtitle><description>Abstract
Antisense transcripts and other long non-coding RNAs are pervasive in mammalian cells, and some of these molecules have been proposed to regulate proximal protein-coding genes in cis. For example, non-coding transcription can contribute to inactivation of tumor suppressor genes in cancer, and antisense transcripts have been implicated in the epigenetic inactivation of imprinted genes. However, our knowledge is still limited and more such regulatory interactions likely await discovery. Here, we make use of available gene expression data from a large compendium of human tumors to generate hypotheses regarding non-coding-to-coding cis-regulatory relationships with emphasis on negative associations, as these are less likely to arise for reasons other than cis-regulation. We document a large number of possible regulatory interactions, including 193 coding/non-coding pairs that show expression patterns compatible with negative cis-regulation. Importantly, by this approach we capture several known cases, and many of the involved coding genes have known roles in cancer. Our study provides a large catalog of putative non-coding/coding cis-regulatory pairs that may serve as a basis for further experimental validation and characterization.</description><subject>cancer</subject><subject>Cell and Molecular Biology</subject><subject>Cell- och molekylärbiologi</subject><subject>chromatin</subject><subject>correlation</subject><subject>evolution</subject><subject>expression</subject><subject>features</subject><subject>Genetics & Heredity</subject><subject>Investigations</subject><subject>landscape</subject><subject>lncRNA</subject><subject>Medical Genetics and Genomics</subject><subject>Medicinsk genetik och genomik</subject><subject>neighboring genes</subject><subject>reveal</subject><subject>RNAseq</subject><subject>transcriptome</subject><issn>2160-1836</issn><issn>2160-1836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9Uk1v1DAQjRCIVqVHrshHLllsx3aSC9KyhXalVamqcrYm9iSkytqLnbTs_-GH4jalHxd8mdGbN29mrJdl7xldMFmIT12xYKxacEp5rV5lh5wpmrOqUK-f5QfZcYzXND0plRLqbXaQ2EqxWhxmf5ZkBSMMvpuQ-JZcTCOM_Q0S08f8ErtpgNGHPVm7EQOYsfcuki843iI6svGuI-fe5cbbPqWX58tIwFlyEfzvfgsDWc2FU3SY2iCiJd4lNAQc5jlLB8M-9pEsTfAxkpMEhojkbNqCI1fT1of4LnvTwhDx-CEeZT--fb1aneWb76fr1XKTG8nFmAMysBWrQbK2kqWRLZeMYm0bKGwNtuCccSFLtJwWreDCtty2kMgFGipNcZStZ13r4VrvQjoh7LWHXt8DPnQawtibAXXTYI1lIZhFK6AWjSwbw2ojjSl5aWnSymeteIu7qXmh1k07naBu0hE1V5USd_zPMz-Rt2gNujHA8KLtZcX1P3Xnb7SsK17xOgl8fBAI_teEcdTbPhocBnDop6g55SUtGSvU0273Xx6wfRzDqL4zlu4KnYylZ2Ml_ofnuz2y_9noabZPl_1f6y80D9jD</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Basu, Swaraj</creator><creator>Larsson, Erik</creator><general>Oxford University Press</general><general>Genetics Society of America</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>F1U</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1400-0119</orcidid><orcidid>https://orcid.org/0000-0001-6107-2487</orcidid></search><sort><creationdate>20180601</creationdate><title>A Catalogue of Putative cis-Regulatory Interactions Between Long Non-coding RNAs and Proximal Coding Genes Based on Correlative Analysis Across Diverse Human Tumors</title><author>Basu, Swaraj ; Larsson, Erik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-ae1ad819a51f857c5f2510e9dba3d9ad32212457ed203f424df2dfa1f83ec05c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>cancer</topic><topic>Cell and Molecular Biology</topic><topic>Cell- och molekylärbiologi</topic><topic>chromatin</topic><topic>correlation</topic><topic>evolution</topic><topic>expression</topic><topic>features</topic><topic>Genetics & Heredity</topic><topic>Investigations</topic><topic>landscape</topic><topic>lncRNA</topic><topic>Medical Genetics and Genomics</topic><topic>Medicinsk genetik och genomik</topic><topic>neighboring genes</topic><topic>reveal</topic><topic>RNAseq</topic><topic>transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Basu, Swaraj</creatorcontrib><creatorcontrib>Larsson, Erik</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Göteborgs universitet</collection><collection>Directory of Open Access Journals</collection><jtitle>G3 : genes - genomes - genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Basu, Swaraj</au><au>Larsson, Erik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Catalogue of Putative cis-Regulatory Interactions Between Long Non-coding RNAs and Proximal Coding Genes Based on Correlative Analysis Across Diverse Human Tumors</atitle><jtitle>G3 : genes - genomes - genetics</jtitle><addtitle>G3 (Bethesda)</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>8</volume><issue>6</issue><spage>2019</spage><epage>2025</epage><pages>2019-2025</pages><issn>2160-1836</issn><eissn>2160-1836</eissn><abstract>Abstract
Antisense transcripts and other long non-coding RNAs are pervasive in mammalian cells, and some of these molecules have been proposed to regulate proximal protein-coding genes in cis. For example, non-coding transcription can contribute to inactivation of tumor suppressor genes in cancer, and antisense transcripts have been implicated in the epigenetic inactivation of imprinted genes. However, our knowledge is still limited and more such regulatory interactions likely await discovery. Here, we make use of available gene expression data from a large compendium of human tumors to generate hypotheses regarding non-coding-to-coding cis-regulatory relationships with emphasis on negative associations, as these are less likely to arise for reasons other than cis-regulation. We document a large number of possible regulatory interactions, including 193 coding/non-coding pairs that show expression patterns compatible with negative cis-regulation. Importantly, by this approach we capture several known cases, and many of the involved coding genes have known roles in cancer. Our study provides a large catalog of putative non-coding/coding cis-regulatory pairs that may serve as a basis for further experimental validation and characterization.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>29666194</pmid><doi>10.1534/g3.118.200296</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1400-0119</orcidid><orcidid>https://orcid.org/0000-0001-6107-2487</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | cancer Cell and Molecular Biology Cell- och molekylärbiologi chromatin correlation evolution expression features Genetics & Heredity Investigations landscape lncRNA Medical Genetics and Genomics Medicinsk genetik och genomik neighboring genes reveal RNAseq transcriptome |
title | A Catalogue of Putative cis-Regulatory Interactions Between Long Non-coding RNAs and Proximal Coding Genes Based on Correlative Analysis Across Diverse Human Tumors |
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