Yannick Cyr, Morgane Gourvest, Grace O Ciabattoni, Tracy Zhang, Alexandra Ac Newman, Tarik Zahr, Sofie Delbare, Florencia Schlamp, Meike Dittmann, Kathryn J Moore, Coen van Solingen
{"title":"lncRNA CARINH调控巨噬细胞中先天免疫转录因子IRF1的表达和功能。","authors":"Yannick Cyr, Morgane Gourvest, Grace O Ciabattoni, Tracy Zhang, Alexandra Ac Newman, Tarik Zahr, Sofie Delbare, Florencia Schlamp, Meike Dittmann, Kathryn J Moore, Coen van Solingen","doi":"10.26508/lsa.202403021","DOIUrl":null,"url":null,"abstract":"<p><p>The discovery of long non-coding RNAs (lncRNAs) has provided a new perspective on the centrality of RNA in gene regulation and genome organization. Here, we screened for lncRNAs with putative functions in the host response to single-stranded RNA respiratory viruses. We identify <i>CARINH</i> as a conserved cis-acting lncRNA up-regulated in three respiratory diseases to control the expression of its antisense gene <i>IRF1</i>, a key transcriptional regulator of the antiviral response. <i>CARINH</i> and <i>IRF1</i> are coordinately increased in the circulation of patients infected with human metapneumovirus, influenza A virus, or SARS-CoV-2, and in macrophages in response to viral infection or TLR3 agonist treatment. Targeted depletion of <i>CARINH</i> or its mouse ortholog <i>Carinh</i> in macrophages reduces the expression of IRF1/Irf1 and their associated target gene networks, increasing susceptibility to viral infection. Accordingly, CRISPR-mediated deletion of <i>Carinh</i> in mice reduces antiviral immunity, increasing viral burden upon sublethal challenge with influenza A virus. Together, these findings identify a conserved role of lncRNA <i>CARINH</i> in coordinating interferon-stimulated genes and antiviral immune responses.</p>","PeriodicalId":18081,"journal":{"name":"Life Science Alliance","volume":"8 3","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11707381/pdf/","citationCount":"0","resultStr":"{\"title\":\"lncRNA <i>CARINH</i> regulates expression and function of innate immune transcription factor IRF1 in macrophages.\",\"authors\":\"Yannick Cyr, Morgane Gourvest, Grace O Ciabattoni, Tracy Zhang, Alexandra Ac Newman, Tarik Zahr, Sofie Delbare, Florencia Schlamp, Meike Dittmann, Kathryn J Moore, Coen van Solingen\",\"doi\":\"10.26508/lsa.202403021\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The discovery of long non-coding RNAs (lncRNAs) has provided a new perspective on the centrality of RNA in gene regulation and genome organization. Here, we screened for lncRNAs with putative functions in the host response to single-stranded RNA respiratory viruses. We identify <i>CARINH</i> as a conserved cis-acting lncRNA up-regulated in three respiratory diseases to control the expression of its antisense gene <i>IRF1</i>, a key transcriptional regulator of the antiviral response. <i>CARINH</i> and <i>IRF1</i> are coordinately increased in the circulation of patients infected with human metapneumovirus, influenza A virus, or SARS-CoV-2, and in macrophages in response to viral infection or TLR3 agonist treatment. Targeted depletion of <i>CARINH</i> or its mouse ortholog <i>Carinh</i> in macrophages reduces the expression of IRF1/Irf1 and their associated target gene networks, increasing susceptibility to viral infection. Accordingly, CRISPR-mediated deletion of <i>Carinh</i> in mice reduces antiviral immunity, increasing viral burden upon sublethal challenge with influenza A virus. Together, these findings identify a conserved role of lncRNA <i>CARINH</i> in coordinating interferon-stimulated genes and antiviral immune responses.</p>\",\"PeriodicalId\":18081,\"journal\":{\"name\":\"Life Science Alliance\",\"volume\":\"8 3\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11707381/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Life Science Alliance\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.26508/lsa.202403021\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Life Science Alliance","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.26508/lsa.202403021","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"Print","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
lncRNA CARINH regulates expression and function of innate immune transcription factor IRF1 in macrophages.
The discovery of long non-coding RNAs (lncRNAs) has provided a new perspective on the centrality of RNA in gene regulation and genome organization. Here, we screened for lncRNAs with putative functions in the host response to single-stranded RNA respiratory viruses. We identify CARINH as a conserved cis-acting lncRNA up-regulated in three respiratory diseases to control the expression of its antisense gene IRF1, a key transcriptional regulator of the antiviral response. CARINH and IRF1 are coordinately increased in the circulation of patients infected with human metapneumovirus, influenza A virus, or SARS-CoV-2, and in macrophages in response to viral infection or TLR3 agonist treatment. Targeted depletion of CARINH or its mouse ortholog Carinh in macrophages reduces the expression of IRF1/Irf1 and their associated target gene networks, increasing susceptibility to viral infection. Accordingly, CRISPR-mediated deletion of Carinh in mice reduces antiviral immunity, increasing viral burden upon sublethal challenge with influenza A virus. Together, these findings identify a conserved role of lncRNA CARINH in coordinating interferon-stimulated genes and antiviral immune responses.
期刊介绍:
Life Science Alliance is a global, open-access, editorially independent, and peer-reviewed journal launched by an alliance of EMBO Press, Rockefeller University Press, and Cold Spring Harbor Laboratory Press. Life Science Alliance is committed to rapid, fair, and transparent publication of valuable research from across all areas in the life sciences.