Head-to-head antisense transcription and R-loop formation promotes transcriptional activation
The mechanisms used by antisense transcripts to regulate their corresponding sense mRNAs are not fully understood. Herein, we have addressed this issue for the vimentin ( VIM ) gene, a member of the intermediate filament family involved in cell and tissue integrity that is deregulated in different t...
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creator | Boque-Sastre, Raquel Soler, Marta Oliveira-Mateos, Cristina Portela, Anna Moutinho, Catia Sayols, Sergi Villanueva, Alberto Esteller, Manel Guil, Sonia |
description | The mechanisms used by antisense transcripts to regulate their corresponding sense mRNAs are not fully understood. Herein, we have addressed this issue for the vimentin ( VIM ) gene, a member of the intermediate filament family involved in cell and tissue integrity that is deregulated in different types of cancer. VIM mRNA levels are positively correlated with the expression of a previously uncharacterized head-to-head antisense transcript, both transcripts being silenced in colon primary tumors concomitant with promoter hypermethylation. Furthermore, antisense transcription promotes formation of an R-loop structure that can be disfavored in vitro and in vivo by ribonuclease H1 overexpression, resulting in VIM down-regulation. Antisense knockdown and R-loop destabilization both result in chromatin compaction around the VIM promoter and a reduction in the binding of transcriptional activators of the NF-κB pathway. These results are the first examples to our knowledge of R-loop–mediated enhancement of gene expression involving head-to-head antisense transcription at a cancer-related locus.
Significance The molecular mechanisms used by noncoding RNAs to regulate gene expression are largely unknown. We have discovered a previously unidentified regulatory phenomenon underlying the transcriptional activation of the intermediate filament protein vimentin. This regulation involves the participation of a previously uncharacterized head-to-head antisense transcript that forms part of a hybrid DNA:RNA structure known as the R loop. R loops have been the focus of recent research regarding their unexpected involvement in gene expression regulation. Antisense-mediated formation of the R loop supports a local chromatin environment that ensures the optimal binding of vimentin transcriptional activators. In addition, we describe how hypermethylation of the locus in a large panel of colon cancer patients is correlated with antisense silencing and, thereby, compromises its regulatory activity. |
doi_str_mv | 10.1073/pnas.1421197112 |
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Significance The molecular mechanisms used by noncoding RNAs to regulate gene expression are largely unknown. We have discovered a previously unidentified regulatory phenomenon underlying the transcriptional activation of the intermediate filament protein vimentin. This regulation involves the participation of a previously uncharacterized head-to-head antisense transcript that forms part of a hybrid DNA:RNA structure known as the R loop. R loops have been the focus of recent research regarding their unexpected involvement in gene expression regulation. Antisense-mediated formation of the R loop supports a local chromatin environment that ensures the optimal binding of vimentin transcriptional activators. In addition, we describe how hypermethylation of the locus in a large panel of colon cancer patients is correlated with antisense silencing and, thereby, compromises its regulatory activity.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1421197112</identifier><identifier>PMID: 25902512</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; Cancer ; Cell Line, Tumor ; Chromatin ; Chromatin - chemistry ; Chromatin Immunoprecipitation ; Colonic Neoplasms - genetics ; Colonic Neoplasms - metabolism ; CpG Islands ; DNA - chemistry ; DNA Methylation ; Gene expression ; Gene Silencing ; Humans ; In Situ Hybridization, Fluorescence ; Models, Molecular ; Nucleic Acid Conformation ; Nucleosomes - chemistry ; Oligonucleotides, Antisense - genetics ; Promoter Regions, Genetic ; Ribonucleic acid ; RNA ; RNA - chemistry ; Transcription, Genetic ; Transcriptional Activation ; Vimentin - genetics</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (18), p.5785-5790</ispartof><rights>Volumes 1–89 and 106–112, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences May 5, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-daff1cf386b6582213b46fc2c862be2f065758a5dd19fce70ec38349a501a7a63</citedby><cites>FETCH-LOGICAL-c557t-daff1cf386b6582213b46fc2c862be2f065758a5dd19fce70ec38349a501a7a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/112/18.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26462663$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26462663$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25902512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boque-Sastre, Raquel</creatorcontrib><creatorcontrib>Soler, Marta</creatorcontrib><creatorcontrib>Oliveira-Mateos, Cristina</creatorcontrib><creatorcontrib>Portela, Anna</creatorcontrib><creatorcontrib>Moutinho, Catia</creatorcontrib><creatorcontrib>Sayols, Sergi</creatorcontrib><creatorcontrib>Villanueva, Alberto</creatorcontrib><creatorcontrib>Esteller, Manel</creatorcontrib><creatorcontrib>Guil, Sonia</creatorcontrib><title>Head-to-head antisense transcription and R-loop formation promotes transcriptional activation</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The mechanisms used by antisense transcripts to regulate their corresponding sense mRNAs are not fully understood. Herein, we have addressed this issue for the vimentin ( VIM ) gene, a member of the intermediate filament family involved in cell and tissue integrity that is deregulated in different types of cancer. VIM mRNA levels are positively correlated with the expression of a previously uncharacterized head-to-head antisense transcript, both transcripts being silenced in colon primary tumors concomitant with promoter hypermethylation. Furthermore, antisense transcription promotes formation of an R-loop structure that can be disfavored in vitro and in vivo by ribonuclease H1 overexpression, resulting in VIM down-regulation. Antisense knockdown and R-loop destabilization both result in chromatin compaction around the VIM promoter and a reduction in the binding of transcriptional activators of the NF-κB pathway. These results are the first examples to our knowledge of R-loop–mediated enhancement of gene expression involving head-to-head antisense transcription at a cancer-related locus.
Significance The molecular mechanisms used by noncoding RNAs to regulate gene expression are largely unknown. We have discovered a previously unidentified regulatory phenomenon underlying the transcriptional activation of the intermediate filament protein vimentin. This regulation involves the participation of a previously uncharacterized head-to-head antisense transcript that forms part of a hybrid DNA:RNA structure known as the R loop. R loops have been the focus of recent research regarding their unexpected involvement in gene expression regulation. Antisense-mediated formation of the R loop supports a local chromatin environment that ensures the optimal binding of vimentin transcriptional activators. In addition, we describe how hypermethylation of the locus in a large panel of colon cancer patients is correlated with antisense silencing and, thereby, compromises its regulatory activity.</description><subject>Biological Sciences</subject><subject>Cancer</subject><subject>Cell Line, Tumor</subject><subject>Chromatin</subject><subject>Chromatin - chemistry</subject><subject>Chromatin Immunoprecipitation</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colonic Neoplasms - metabolism</subject><subject>CpG Islands</subject><subject>DNA - chemistry</subject><subject>DNA Methylation</subject><subject>Gene expression</subject><subject>Gene Silencing</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Models, Molecular</subject><subject>Nucleic Acid Conformation</subject><subject>Nucleosomes - chemistry</subject><subject>Oligonucleotides, Antisense - genetics</subject><subject>Promoter Regions, Genetic</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA - chemistry</subject><subject>Transcription, Genetic</subject><subject>Transcriptional Activation</subject><subject>Vimentin - genetics</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi0EokvhzAmI1AuXtDMT23EuSKgqFKkSEtAjsryO3WaVxMHOVuLf4_1gl3IaaeaZRzN6GXuNcI5QVxfTaNI5ckJsakR6whYIDZaSN_CULQCoLhUnfsJepLQCgEYoeM5OSDRAAmnBfl4705ZzKO9zLcw4d8mNyRVzNGOysZvmLoy53xbfyj6EqfAhDmbbnGIYwuzSY9b0hbFz97BlXrJn3vTJvdrXU3b76erH5XV58_Xzl8uPN6UVop7L1niP1ldKLqVQRFgtufSWrJK0dORBilooI9oWG29dDc5WquKNEYCmNrI6ZR923mm9HFxr3Zhv6vUUu8HE3zqYTj-ejN29vgsPmnOSXKgseL8XxPBr7dKshy5Z1_dmdGGdNEoFqCQSZfTsP3QV1jH_vaWoAdlglamLHWVjSCk6fzgGQW-i05vo9DG6vPH23x8O_N-sMvBuD2w2DzokjUqLWolMvNkRqzSHeDRILknK6mjwJmhzF7ukb78ToARADlU2_AGVsrP6</recordid><startdate>20150505</startdate><enddate>20150505</enddate><creator>Boque-Sastre, Raquel</creator><creator>Soler, Marta</creator><creator>Oliveira-Mateos, Cristina</creator><creator>Portela, Anna</creator><creator>Moutinho, Catia</creator><creator>Sayols, Sergi</creator><creator>Villanueva, Alberto</creator><creator>Esteller, Manel</creator><creator>Guil, Sonia</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150505</creationdate><title>Head-to-head antisense transcription and R-loop formation promotes transcriptional activation</title><author>Boque-Sastre, Raquel ; 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Herein, we have addressed this issue for the vimentin ( VIM ) gene, a member of the intermediate filament family involved in cell and tissue integrity that is deregulated in different types of cancer. VIM mRNA levels are positively correlated with the expression of a previously uncharacterized head-to-head antisense transcript, both transcripts being silenced in colon primary tumors concomitant with promoter hypermethylation. Furthermore, antisense transcription promotes formation of an R-loop structure that can be disfavored in vitro and in vivo by ribonuclease H1 overexpression, resulting in VIM down-regulation. Antisense knockdown and R-loop destabilization both result in chromatin compaction around the VIM promoter and a reduction in the binding of transcriptional activators of the NF-κB pathway. These results are the first examples to our knowledge of R-loop–mediated enhancement of gene expression involving head-to-head antisense transcription at a cancer-related locus.
Significance The molecular mechanisms used by noncoding RNAs to regulate gene expression are largely unknown. We have discovered a previously unidentified regulatory phenomenon underlying the transcriptional activation of the intermediate filament protein vimentin. This regulation involves the participation of a previously uncharacterized head-to-head antisense transcript that forms part of a hybrid DNA:RNA structure known as the R loop. R loops have been the focus of recent research regarding their unexpected involvement in gene expression regulation. Antisense-mediated formation of the R loop supports a local chromatin environment that ensures the optimal binding of vimentin transcriptional activators. In addition, we describe how hypermethylation of the locus in a large panel of colon cancer patients is correlated with antisense silencing and, thereby, compromises its regulatory activity.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>25902512</pmid><doi>10.1073/pnas.1421197112</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological Sciences Cancer Cell Line, Tumor Chromatin Chromatin - chemistry Chromatin Immunoprecipitation Colonic Neoplasms - genetics Colonic Neoplasms - metabolism CpG Islands DNA - chemistry DNA Methylation Gene expression Gene Silencing Humans In Situ Hybridization, Fluorescence Models, Molecular Nucleic Acid Conformation Nucleosomes - chemistry Oligonucleotides, Antisense - genetics Promoter Regions, Genetic Ribonucleic acid RNA RNA - chemistry Transcription, Genetic Transcriptional Activation Vimentin - genetics |
title | Head-to-head antisense transcription and R-loop formation promotes transcriptional activation |
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