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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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6463213</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2199188806</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5191-f11bba19c80cf62668b85411bb9ed7f5004a22d100858ef32a692ff36f32aec83</originalsourceid><addsrcrecordid>eNqFkUtP3DAUha2KqgyPfVcoEhs2ob5O4tgSqkRHUKA8JETXlpO5Dhkl9tSeAPPv62F4FKSKla_s7xzd40PIV6D7ULCCfcO-mu4zCgIopTl8IiPIOU0ZLYs1MqKMQ5qDkOtkI4RpRApRwheynlEJglIxIuObW0w6Z5vEOlu7SRun68vD5Ppq_Os08dgMnZ5jSFprOt33eu78ImnQYoIPM48htM5ukc9GdwG3n85N8vv46GZ8kp5f_TwdH56ndQESUgNQVRpkLWhtOONcVKLIl5cSJ6UpYgDN2CQmEYVAkzHNJTMm48sRa5Ftku8r39lQ9Tip0c697tTMt732C-V0q96-2PZWNe5O8ZxnDLJosPdk4N2fAcNc9W2oseu0RTcExUDGfxGC8ojuvkOnbvA2xlOMUZlLKGUZKbqiau9C8GhelgGqHhtSy4bUa0NRsvNviBfBcyUROFgB922Hiw8N1dHFj7M3_rCSh6i0DfrXxf-701_XRK0J</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2209491797</pqid></control><display><type>article</type><title>The long noncoding RNA ROCKI regulates inflammatory gene expression</title><source>Wiley Free Content</source><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature OA Free Journals</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 & 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 & 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 & 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 & 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 & 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> |
fulltext | fulltext |
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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