A conserved enhancer regulates Il9 expression in multiple lineages
dc.contributor.author | Koh, Byunghee | |
dc.contributor.author | Qayum, Amina Abdul | |
dc.contributor.author | Srivastava, Rajneesh | |
dc.contributor.author | Fu, Yongyao | |
dc.contributor.author | Ulrich, Benjamin J. | |
dc.contributor.author | Janga, Sarath Chandra | |
dc.contributor.author | Kaplan, Mark H. | |
dc.contributor.department | Pediatrics, School of Medicine | en_US |
dc.date.accessioned | 2019-06-14T14:22:22Z | |
dc.date.available | 2019-06-14T14:22:22Z | |
dc.date.issued | 2018-11-15 | |
dc.description.abstract | Cytokine genes are regulated by multiple regulatory elements that confer tissue-specific and activation-dependent expression. The cis-regulatory elements of the gene encoding IL-9, a cytokine that promotes allergy, autoimmune inflammation and tumor immunity, have not been defined. Here we identify an enhancer (CNS-25) upstream of the Il9 gene that binds most transcription factors (TFs) that promote Il9 gene expression. Deletion of the enhancer in the mouse germline alters transcription factor binding to the remaining Il9 regulatory elements, and results in diminished IL-9 production in multiple cell types including Th9 cells, and attenuates IL-9-dependent immune responses. Moreover, deletion of the homologous enhancer (CNS-18) in primary human Th9 cultures results in significant decrease of IL-9 production. Thus, Il9 CNS-25/IL9 CNS-18 is a critical and conserved regulatory element for IL-9 production. | en_US |
dc.eprint.version | Final published version | en_US |
dc.identifier.citation | Koh, B., Abdul Qayum, A., Srivastava, R., Fu, Y., Ulrich, B. J., Janga, S. C., & Kaplan, M. H. (2018). A conserved enhancer regulates Il9 expression in multiple lineages. Nature communications, 9(1), 4803. doi:10.1038/s41467-018-07202-0 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/19616 | |
dc.language.iso | en_US | en_US |
dc.publisher | Nature Research | en_US |
dc.relation.isversionof | 10.1038/s41467-018-07202-0 | en_US |
dc.relation.journal | Nature Communications | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/us | * |
dc.source | PMC | en_US |
dc.subject | Binding Sites | en_US |
dc.subject | CRISPR-Cas Systems | en_US |
dc.subject | Cell Differentiation | en_US |
dc.subject | Cell Lineage | en_US |
dc.subject | Conserved Sequence | en_US |
dc.subject | Enhancer Elements, Genetic | en_US |
dc.subject | Gene Editing | en_US |
dc.subject | Gene Expression Regulation | en_US |
dc.subject | Interleukin-9 | en_US |
dc.subject | Mice, Inbred C57BL | en_US |
dc.subject | Mice, Knockout | en_US |
dc.subject | Primary Cell Culture | en_US |
dc.subject | Protein Binding | en_US |
dc.subject | T-Lymphocytes, Helper-Inducer | en_US |
dc.title | A conserved enhancer regulates Il9 expression in multiple lineages | en_US |
dc.type | Article | en_US |
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