The long noncoding RNA ROCKI regulates inflammatory gene expression

Long noncoding RNAs (lncRNAs) can regulate target gene expression by acting in cis (locally) or in trans (non‐locally). Here, we performed genome‐wide expression analysis of Toll‐like receptor (TLR)‐stimulated human macrophages to identify pairs of cis ‐acting lncRNAs and protein‐coding genes involv...

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Veröffentlicht in:The EMBO journal 2019-04, Vol.38 (8), p.n/a
Hauptverfasser: Zhang, Qiong, Chao, Ti‐Chun, Patil, Veena S, Qin, Yue, Tiwari, Shashi Kant, Chiou, Joshua, Dobin, Alexander, Tsai, Chih‐Ming, Li, Zhonghan, Dang, Jason, Gupta, Shagun, Urdahl, Kevin, Nizet, Victor, Gingeras, Thomas R, Gaulton, Kyle J, Rana, Tariq M
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container_title The EMBO journal
container_volume 38
creator Zhang, Qiong
Chao, Ti‐Chun
Patil, Veena S
Qin, Yue
Tiwari, Shashi Kant
Chiou, Joshua
Dobin, Alexander
Tsai, Chih‐Ming
Li, Zhonghan
Dang, Jason
Gupta, Shagun
Urdahl, Kevin
Nizet, Victor
Gingeras, Thomas R
Gaulton, Kyle J
Rana, Tariq M
description Long noncoding RNAs (lncRNAs) can regulate target gene expression by acting in cis (locally) or in trans (non‐locally). Here, we performed genome‐wide expression analysis of Toll‐like receptor (TLR)‐stimulated human macrophages to identify pairs of cis ‐acting lncRNAs and protein‐coding genes involved in innate immunity. A total of 229 gene pairs were identified, many of which were commonly regulated by signaling through multiple TLRs and were involved in the cytokine responses to infection by group B Streptococcus . We focused on elucidating the function of one lncRNA, named lnc‐MARCKS or ROCKI (Regulator of Cytokines and Inflammation), which was induced by multiple TLR stimuli and acted as a master regulator of inflammatory responses. ROCKI interacted with APEX1 (apurinic/apyrimidinic endodeoxyribonuclease 1) to form a ribonucleoprotein complex at the MARCKS promoter. In turn, ROCKI –APEX1 recruited the histone deacetylase HDAC1, which removed the H3K27ac modification from the promoter, thus reducing MARCKS transcription and subsequent Ca 2+ signaling and inflammatory gene expression. Finally, genetic variants affecting ROCKI expression were linked to a reduced risk of certain inflammatory and infectious disease in humans, including inflammatory bowel disease and tuberculosis. Collectively, these data highlight the importance of cis ‐acting lncRNAs in TLR signaling, innate immunity, and pathophysiological inflammation. Synopsis Activation of Toll‐like receptors (TLRs) induced expression changes in lncRNAs that regulate their neighboring genes involved in inflammation. A lncRNA named ROCKI forms a ribonucleoprotein complex and controls inflammatory responses via chromatin modification. More than 200 cis ‐acting lncRNAs and protein‐coding gene pairs were identified in TLR‐stimulated macrophages. Lnc‐MARCKS , also designated ROCKI , is a master regulator of inflammatory responses to TLR ligands. ROCKI interacts with APEX1 and HDAC1 enzymes at the MARCKS promoter. ROCKI expression is significantly associated with inflammation‐ and infection‐related disease phenotypes in humans. Graphical Abstract Genome‐wide identification of cis ‐acting lncRNAs that regulate gene expression in response to infection identify a Toll‐like receptor‐induced upstream regulator of calcium signalling and inflammation processes, associated with inflammatory or infectious disease pathologies in humans.
doi_str_mv 10.15252/embj.2018100041
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Here, we performed genome‐wide expression analysis of Toll‐like receptor (TLR)‐stimulated human macrophages to identify pairs of cis ‐acting lncRNAs and protein‐coding genes involved in innate immunity. A total of 229 gene pairs were identified, many of which were commonly regulated by signaling through multiple TLRs and were involved in the cytokine responses to infection by group B Streptococcus . We focused on elucidating the function of one lncRNA, named lnc‐MARCKS or ROCKI (Regulator of Cytokines and Inflammation), which was induced by multiple TLR stimuli and acted as a master regulator of inflammatory responses. ROCKI interacted with APEX1 (apurinic/apyrimidinic endodeoxyribonuclease 1) to form a ribonucleoprotein complex at the MARCKS promoter. In turn, ROCKI –APEX1 recruited the histone deacetylase HDAC1, which removed the H3K27ac modification from the promoter, thus reducing MARCKS transcription and subsequent Ca 2+ signaling and inflammatory gene expression. Finally, genetic variants affecting ROCKI expression were linked to a reduced risk of certain inflammatory and infectious disease in humans, including inflammatory bowel disease and tuberculosis. Collectively, these data highlight the importance of cis ‐acting lncRNAs in TLR signaling, innate immunity, and pathophysiological inflammation. Synopsis Activation of Toll‐like receptors (TLRs) induced expression changes in lncRNAs that regulate their neighboring genes involved in inflammation. A lncRNA named ROCKI forms a ribonucleoprotein complex and controls inflammatory responses via chromatin modification. More than 200 cis ‐acting lncRNAs and protein‐coding gene pairs were identified in TLR‐stimulated macrophages. Lnc‐MARCKS , also designated ROCKI , is a master regulator of inflammatory responses to TLR ligands. ROCKI interacts with APEX1 and HDAC1 enzymes at the MARCKS promoter. ROCKI expression is significantly associated with inflammation‐ and infection‐related disease phenotypes in humans. Graphical Abstract Genome‐wide identification of cis ‐acting lncRNAs that regulate gene expression in response to infection identify a Toll‐like receptor‐induced upstream regulator of calcium signalling and inflammation processes, associated with inflammatory or infectious disease pathologies in humans.</description><identifier>ISSN: 0261-4189</identifier><identifier>ISSN: 1460-2075</identifier><identifier>EISSN: 1460-2075</identifier><identifier>DOI: 10.15252/embj.2018100041</identifier><identifier>PMID: 30918008</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Calcium ions ; Calcium signalling ; Cells, Cultured ; Chromatin ; cytokine production ; Cytokines ; Cytokines - metabolism ; DNA-(Apurinic or Apyrimidinic Site) Lyase - genetics ; DNA-(Apurinic or Apyrimidinic Site) Lyase - metabolism ; EMBO19 ; EMBO23 ; EMBO36 ; Gene expression ; Gene Expression Regulation ; Genes ; Genetic diversity ; Genetic variance ; Genome, Human ; Genomes ; Histone deacetylase ; Histone Deacetylase 1 - genetics ; Histone Deacetylase 1 - metabolism ; host–pathogen interactions ; Humans ; Immune system ; Immunity ; Immunity, Innate - immunology ; Infectious diseases ; Inflammation ; Inflammation - genetics ; Inflammation - immunology ; Inflammation - microbiology ; Inflammatory bowel diseases ; innate immune system ; Innate immunity ; Intestine ; Kinases ; lncRNA ; Macrophages ; Macrophages - immunology ; Macrophages - metabolism ; Macrophages - microbiology ; MARCKS protein ; Myristoylated Alanine-Rich C Kinase Substrate - genetics ; Myristoylated Alanine-Rich C Kinase Substrate - metabolism ; Phenotypes ; Promoter Regions, Genetic ; Proteins ; Receptors ; Ribonucleic acid ; Risk management ; RNA ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Streptococcal Infections - immunology ; Streptococcal Infections - microbiology ; Streptococcus agalactiae - isolation &amp; purification ; Streptococcus infections ; TLRs ; Toll-like receptors ; Toll-Like Receptors - genetics ; Toll-Like Receptors - metabolism ; Transcription ; Tuberculosis</subject><ispartof>The EMBO journal, 2019-04, Vol.38 (8), p.n/a</ispartof><rights>The Author(s) 2019</rights><rights>2019 The Authors. Published under the terms of the CC BY NC ND 4.0 license</rights><rights>2019 The Authors. Published under the terms of the CC BY NC ND 4.0 license.</rights><rights>2019 EMBO</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5191-f11bba19c80cf62668b85411bb9ed7f5004a22d100858ef32a692ff36f32aec83</citedby><cites>FETCH-LOGICAL-c5191-f11bba19c80cf62668b85411bb9ed7f5004a22d100858ef32a692ff36f32aec83</cites><orcidid>0000-0002-4618-0647 ; 0000-0001-9558-5766 ; 0000-0003-3847-0422</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/PMC6463213/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463213/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,1427,27901,27902,41096,42165,45550,45551,46384,46808,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30918008$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Qiong</creatorcontrib><creatorcontrib>Chao, Ti‐Chun</creatorcontrib><creatorcontrib>Patil, Veena S</creatorcontrib><creatorcontrib>Qin, Yue</creatorcontrib><creatorcontrib>Tiwari, Shashi Kant</creatorcontrib><creatorcontrib>Chiou, Joshua</creatorcontrib><creatorcontrib>Dobin, Alexander</creatorcontrib><creatorcontrib>Tsai, Chih‐Ming</creatorcontrib><creatorcontrib>Li, Zhonghan</creatorcontrib><creatorcontrib>Dang, Jason</creatorcontrib><creatorcontrib>Gupta, Shagun</creatorcontrib><creatorcontrib>Urdahl, Kevin</creatorcontrib><creatorcontrib>Nizet, Victor</creatorcontrib><creatorcontrib>Gingeras, Thomas R</creatorcontrib><creatorcontrib>Gaulton, Kyle J</creatorcontrib><creatorcontrib>Rana, Tariq M</creatorcontrib><title>The long noncoding RNA ROCKI regulates inflammatory gene expression</title><title>The EMBO journal</title><addtitle>EMBO J</addtitle><addtitle>EMBO J</addtitle><description>Long noncoding RNAs (lncRNAs) can regulate target gene expression by acting in cis (locally) or in trans (non‐locally). Here, we performed genome‐wide expression analysis of Toll‐like receptor (TLR)‐stimulated human macrophages to identify pairs of cis ‐acting lncRNAs and protein‐coding genes involved in innate immunity. A total of 229 gene pairs were identified, many of which were commonly regulated by signaling through multiple TLRs and were involved in the cytokine responses to infection by group B Streptococcus . We focused on elucidating the function of one lncRNA, named lnc‐MARCKS or ROCKI (Regulator of Cytokines and Inflammation), which was induced by multiple TLR stimuli and acted as a master regulator of inflammatory responses. ROCKI interacted with APEX1 (apurinic/apyrimidinic endodeoxyribonuclease 1) to form a ribonucleoprotein complex at the MARCKS promoter. In turn, ROCKI –APEX1 recruited the histone deacetylase HDAC1, which removed the H3K27ac modification from the promoter, thus reducing MARCKS transcription and subsequent Ca 2+ signaling and inflammatory gene expression. Finally, genetic variants affecting ROCKI expression were linked to a reduced risk of certain inflammatory and infectious disease in humans, including inflammatory bowel disease and tuberculosis. Collectively, these data highlight the importance of cis ‐acting lncRNAs in TLR signaling, innate immunity, and pathophysiological inflammation. Synopsis Activation of Toll‐like receptors (TLRs) induced expression changes in lncRNAs that regulate their neighboring genes involved in inflammation. A lncRNA named ROCKI forms a ribonucleoprotein complex and controls inflammatory responses via chromatin modification. More than 200 cis ‐acting lncRNAs and protein‐coding gene pairs were identified in TLR‐stimulated macrophages. Lnc‐MARCKS , also designated ROCKI , is a master regulator of inflammatory responses to TLR ligands. ROCKI interacts with APEX1 and HDAC1 enzymes at the MARCKS promoter. ROCKI expression is significantly associated with inflammation‐ and infection‐related disease phenotypes in humans. Graphical Abstract Genome‐wide identification of cis ‐acting lncRNAs that regulate gene expression in response to infection identify a Toll‐like receptor‐induced upstream regulator of calcium signalling and inflammation processes, associated with inflammatory or infectious disease pathologies in humans.</description><subject>Calcium ions</subject><subject>Calcium signalling</subject><subject>Cells, Cultured</subject><subject>Chromatin</subject><subject>cytokine production</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>DNA-(Apurinic or Apyrimidinic Site) Lyase - genetics</subject><subject>DNA-(Apurinic or Apyrimidinic Site) Lyase - metabolism</subject><subject>EMBO19</subject><subject>EMBO23</subject><subject>EMBO36</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Genes</subject><subject>Genetic diversity</subject><subject>Genetic variance</subject><subject>Genome, Human</subject><subject>Genomes</subject><subject>Histone deacetylase</subject><subject>Histone Deacetylase 1 - genetics</subject><subject>Histone Deacetylase 1 - metabolism</subject><subject>host–pathogen interactions</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunity</subject><subject>Immunity, Innate - immunology</subject><subject>Infectious diseases</subject><subject>Inflammation</subject><subject>Inflammation - genetics</subject><subject>Inflammation - immunology</subject><subject>Inflammation - microbiology</subject><subject>Inflammatory bowel diseases</subject><subject>innate immune system</subject><subject>Innate immunity</subject><subject>Intestine</subject><subject>Kinases</subject><subject>lncRNA</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - microbiology</subject><subject>MARCKS protein</subject><subject>Myristoylated Alanine-Rich C Kinase Substrate - genetics</subject><subject>Myristoylated Alanine-Rich C Kinase Substrate - metabolism</subject><subject>Phenotypes</subject><subject>Promoter Regions, Genetic</subject><subject>Proteins</subject><subject>Receptors</subject><subject>Ribonucleic acid</subject><subject>Risk management</subject><subject>RNA</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Streptococcal Infections - immunology</subject><subject>Streptococcal Infections - microbiology</subject><subject>Streptococcus agalactiae - isolation &amp; purification</subject><subject>Streptococcus infections</subject><subject>TLRs</subject><subject>Toll-like receptors</subject><subject>Toll-Like Receptors - genetics</subject><subject>Toll-Like Receptors - metabolism</subject><subject>Transcription</subject><subject>Tuberculosis</subject><issn>0261-4189</issn><issn>1460-2075</issn><issn>1460-2075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNqFkUtP3DAUha2KqgyPfVcoEhs2ob5O4tgSqkRHUKA8JETXlpO5Dhkl9tSeAPPv62F4FKSKla_s7xzd40PIV6D7ULCCfcO-mu4zCgIopTl8IiPIOU0ZLYs1MqKMQ5qDkOtkI4RpRApRwheynlEJglIxIuObW0w6Z5vEOlu7SRun68vD5Ppq_Os08dgMnZ5jSFprOt33eu78ImnQYoIPM48htM5ukc9GdwG3n85N8vv46GZ8kp5f_TwdH56ndQESUgNQVRpkLWhtOONcVKLIl5cSJ6UpYgDN2CQmEYVAkzHNJTMm48sRa5Ftku8r39lQ9Tip0c697tTMt732C-V0q96-2PZWNe5O8ZxnDLJosPdk4N2fAcNc9W2oseu0RTcExUDGfxGC8ojuvkOnbvA2xlOMUZlLKGUZKbqiau9C8GhelgGqHhtSy4bUa0NRsvNviBfBcyUROFgB922Hiw8N1dHFj7M3_rCSh6i0DfrXxf-701_XRK0J</recordid><startdate>20190415</startdate><enddate>20190415</enddate><creator>Zhang, Qiong</creator><creator>Chao, Ti‐Chun</creator><creator>Patil, Veena S</creator><creator>Qin, Yue</creator><creator>Tiwari, Shashi Kant</creator><creator>Chiou, Joshua</creator><creator>Dobin, Alexander</creator><creator>Tsai, Chih‐Ming</creator><creator>Li, Zhonghan</creator><creator>Dang, Jason</creator><creator>Gupta, Shagun</creator><creator>Urdahl, Kevin</creator><creator>Nizet, Victor</creator><creator>Gingeras, Thomas R</creator><creator>Gaulton, Kyle J</creator><creator>Rana, Tariq M</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>John Wiley and Sons Inc</general><scope>C6C</scope><scope>24P</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>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>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4618-0647</orcidid><orcidid>https://orcid.org/0000-0001-9558-5766</orcidid><orcidid>https://orcid.org/0000-0003-3847-0422</orcidid></search><sort><creationdate>20190415</creationdate><title>The long noncoding RNA ROCKI regulates inflammatory gene expression</title><author>Zhang, Qiong ; Chao, Ti‐Chun ; Patil, Veena S ; Qin, Yue ; Tiwari, Shashi Kant ; Chiou, Joshua ; Dobin, Alexander ; Tsai, Chih‐Ming ; Li, Zhonghan ; Dang, Jason ; Gupta, Shagun ; Urdahl, Kevin ; Nizet, Victor ; Gingeras, Thomas R ; Gaulton, Kyle J ; Rana, Tariq M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5191-f11bba19c80cf62668b85411bb9ed7f5004a22d100858ef32a692ff36f32aec83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Calcium ions</topic><topic>Calcium signalling</topic><topic>Cells, Cultured</topic><topic>Chromatin</topic><topic>cytokine production</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>DNA-(Apurinic or Apyrimidinic Site) Lyase - genetics</topic><topic>DNA-(Apurinic or Apyrimidinic Site) Lyase - metabolism</topic><topic>EMBO19</topic><topic>EMBO23</topic><topic>EMBO36</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Genes</topic><topic>Genetic diversity</topic><topic>Genetic variance</topic><topic>Genome, Human</topic><topic>Genomes</topic><topic>Histone deacetylase</topic><topic>Histone Deacetylase 1 - genetics</topic><topic>Histone Deacetylase 1 - metabolism</topic><topic>host–pathogen interactions</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunity</topic><topic>Immunity, Innate - immunology</topic><topic>Infectious diseases</topic><topic>Inflammation</topic><topic>Inflammation - genetics</topic><topic>Inflammation - immunology</topic><topic>Inflammation - microbiology</topic><topic>Inflammatory bowel diseases</topic><topic>innate immune system</topic><topic>Innate immunity</topic><topic>Intestine</topic><topic>Kinases</topic><topic>lncRNA</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - microbiology</topic><topic>MARCKS protein</topic><topic>Myristoylated Alanine-Rich C Kinase Substrate - genetics</topic><topic>Myristoylated Alanine-Rich C Kinase Substrate - metabolism</topic><topic>Phenotypes</topic><topic>Promoter Regions, Genetic</topic><topic>Proteins</topic><topic>Receptors</topic><topic>Ribonucleic acid</topic><topic>Risk management</topic><topic>RNA</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Streptococcal Infections - immunology</topic><topic>Streptococcal Infections - microbiology</topic><topic>Streptococcus agalactiae - isolation &amp; purification</topic><topic>Streptococcus infections</topic><topic>TLRs</topic><topic>Toll-like receptors</topic><topic>Toll-Like Receptors - genetics</topic><topic>Toll-Like Receptors - metabolism</topic><topic>Transcription</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Qiong</creatorcontrib><creatorcontrib>Chao, Ti‐Chun</creatorcontrib><creatorcontrib>Patil, Veena S</creatorcontrib><creatorcontrib>Qin, Yue</creatorcontrib><creatorcontrib>Tiwari, Shashi Kant</creatorcontrib><creatorcontrib>Chiou, Joshua</creatorcontrib><creatorcontrib>Dobin, Alexander</creatorcontrib><creatorcontrib>Tsai, Chih‐Ming</creatorcontrib><creatorcontrib>Li, Zhonghan</creatorcontrib><creatorcontrib>Dang, Jason</creatorcontrib><creatorcontrib>Gupta, Shagun</creatorcontrib><creatorcontrib>Urdahl, Kevin</creatorcontrib><creatorcontrib>Nizet, Victor</creatorcontrib><creatorcontrib>Gingeras, Thomas R</creatorcontrib><creatorcontrib>Gaulton, Kyle J</creatorcontrib><creatorcontrib>Rana, Tariq M</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors 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>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The EMBO journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Qiong</au><au>Chao, Ti‐Chun</au><au>Patil, Veena S</au><au>Qin, Yue</au><au>Tiwari, Shashi Kant</au><au>Chiou, Joshua</au><au>Dobin, Alexander</au><au>Tsai, Chih‐Ming</au><au>Li, Zhonghan</au><au>Dang, Jason</au><au>Gupta, Shagun</au><au>Urdahl, Kevin</au><au>Nizet, Victor</au><au>Gingeras, Thomas R</au><au>Gaulton, Kyle J</au><au>Rana, Tariq M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The long noncoding RNA ROCKI regulates inflammatory gene expression</atitle><jtitle>The EMBO journal</jtitle><stitle>EMBO J</stitle><addtitle>EMBO J</addtitle><date>2019-04-15</date><risdate>2019</risdate><volume>38</volume><issue>8</issue><epage>n/a</epage><issn>0261-4189</issn><issn>1460-2075</issn><eissn>1460-2075</eissn><abstract>Long noncoding RNAs (lncRNAs) can regulate target gene expression by acting in cis (locally) or in trans (non‐locally). Here, we performed genome‐wide expression analysis of Toll‐like receptor (TLR)‐stimulated human macrophages to identify pairs of cis ‐acting lncRNAs and protein‐coding genes involved in innate immunity. A total of 229 gene pairs were identified, many of which were commonly regulated by signaling through multiple TLRs and were involved in the cytokine responses to infection by group B Streptococcus . We focused on elucidating the function of one lncRNA, named lnc‐MARCKS or ROCKI (Regulator of Cytokines and Inflammation), which was induced by multiple TLR stimuli and acted as a master regulator of inflammatory responses. ROCKI interacted with APEX1 (apurinic/apyrimidinic endodeoxyribonuclease 1) to form a ribonucleoprotein complex at the MARCKS promoter. In turn, ROCKI –APEX1 recruited the histone deacetylase HDAC1, which removed the H3K27ac modification from the promoter, thus reducing MARCKS transcription and subsequent Ca 2+ signaling and inflammatory gene expression. Finally, genetic variants affecting ROCKI expression were linked to a reduced risk of certain inflammatory and infectious disease in humans, including inflammatory bowel disease and tuberculosis. Collectively, these data highlight the importance of cis ‐acting lncRNAs in TLR signaling, innate immunity, and pathophysiological inflammation. Synopsis Activation of Toll‐like receptors (TLRs) induced expression changes in lncRNAs that regulate their neighboring genes involved in inflammation. A lncRNA named ROCKI forms a ribonucleoprotein complex and controls inflammatory responses via chromatin modification. More than 200 cis ‐acting lncRNAs and protein‐coding gene pairs were identified in TLR‐stimulated macrophages. Lnc‐MARCKS , also designated ROCKI , is a master regulator of inflammatory responses to TLR ligands. ROCKI interacts with APEX1 and HDAC1 enzymes at the MARCKS promoter. ROCKI expression is significantly associated with inflammation‐ and infection‐related disease phenotypes in humans. Graphical Abstract Genome‐wide identification of cis ‐acting lncRNAs that regulate gene expression in response to infection identify a Toll‐like receptor‐induced upstream regulator of calcium signalling and inflammation processes, associated with inflammatory or infectious disease pathologies in humans.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30918008</pmid><doi>10.15252/embj.2018100041</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0002-4618-0647</orcidid><orcidid>https://orcid.org/0000-0001-9558-5766</orcidid><orcidid>https://orcid.org/0000-0003-3847-0422</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0261-4189
ispartof The EMBO journal, 2019-04, Vol.38 (8), p.n/a
issn 0261-4189
1460-2075
1460-2075
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6463213
source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature OA Free Journals
subjects Calcium ions
Calcium signalling
Cells, Cultured
Chromatin
cytokine production
Cytokines
Cytokines - metabolism
DNA-(Apurinic or Apyrimidinic Site) Lyase - genetics
DNA-(Apurinic or Apyrimidinic Site) Lyase - metabolism
EMBO19
EMBO23
EMBO36
Gene expression
Gene Expression Regulation
Genes
Genetic diversity
Genetic variance
Genome, Human
Genomes
Histone deacetylase
Histone Deacetylase 1 - genetics
Histone Deacetylase 1 - metabolism
host–pathogen interactions
Humans
Immune system
Immunity
Immunity, Innate - immunology
Infectious diseases
Inflammation
Inflammation - genetics
Inflammation - immunology
Inflammation - microbiology
Inflammatory bowel diseases
innate immune system
Innate immunity
Intestine
Kinases
lncRNA
Macrophages
Macrophages - immunology
Macrophages - metabolism
Macrophages - microbiology
MARCKS protein
Myristoylated Alanine-Rich C Kinase Substrate - genetics
Myristoylated Alanine-Rich C Kinase Substrate - metabolism
Phenotypes
Promoter Regions, Genetic
Proteins
Receptors
Ribonucleic acid
Risk management
RNA
RNA, Long Noncoding - genetics
RNA, Long Noncoding - metabolism
Streptococcal Infections - immunology
Streptococcal Infections - microbiology
Streptococcus agalactiae - isolation & purification
Streptococcus infections
TLRs
Toll-like receptors
Toll-Like Receptors - genetics
Toll-Like Receptors - metabolism
Transcription
Tuberculosis
title The long noncoding RNA ROCKI regulates inflammatory gene expression
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