IIott, NE, Heward, JA, Roux, B, Tsitsiou, E, Fenwick, PS, Lenzi, L, Goodhead, I, Hertz-Fowler, C, Heger, A, Hall, N, Donnelly, LE, Sims, D and Lindsay, MA 2014, 'Long non-coding RNAs and enhancer RNAs regulate the lipopolysaccharide-induced inflammatory response in human monocytes' , Nature Communications, 5 , p. 3979.
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Early reports indicate that long non-coding RNAs (lncRNAs) are novel regulators of biological responses. However, their role in the human innate immune response, which provides the initial defence against infection, is largely unexplored. To address this issue, here we characterize the long non-coding RNA transcriptome in primary human monocytes using RNA sequencing. We identify 76 enhancer RNAs (eRNAs), 40 canonical lncRNAs, 65 antisense lncRNAs and 35 regions of bidirectional transcription (RBT) that are differentially expressed in response to bacterial lipopolysaccharide (LPS). Crucially, we demonstrate that knockdown of nuclear-localized, NF-κB-regulated, eRNAs (IL1β-eRNA) and RBT (IL1β-RBT46) surrounding the IL1β locus, attenuates LPS-induced messenger RNA transcription and release of the proinflammatory mediators, IL1β and CXCL8. We predict that lncRNAs can be important regulators of the human innate immune response.
|Themes:||Subjects outside of the University Themes|
|Schools:||Schools > School of Environment and Life Sciences > Ecosystems and Environment Research Centre|
|Journal or Publication Title:||Nature Communications|
|Publisher:||Nature Publishing Group|
|Funders:||Biotechnology and Biosciences Sciences Research Council (BBSRC), Medical Research Council (MRC)|
|Depositing User:||Dr Ian Goodhead|
|Date Deposited:||23 Sep 2015 17:04|
|Last Modified:||25 Sep 2015 10:12|
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