| Literature DB >> 25419628 |
Elizabeth K Flynn1, Bojan Vilagos2, Udochuku Richson2, David E Symer1,3, Alan Aderem4, Christopher Schliehe2, Savitha Swaminanthan4, Berislav Bosnjak5, Lisa Bauer2, Richard K Kandasamy2, Isabel M Griesshammer2, Lindsay Kosack2, Frank Schmitz4, Vladimir Litvak6, James Sissons4, Alexander Lercher2, Anannya Bhattacharya2, Kseniya Khamina2, Anna L Trivett1, Lino Tessarollo1, Ildiko Mesteri7, Anastasiya Hladik2,8, Doron Merkler9,10, Stefan Kubicek2, Sylvia Knapp2,8, Michelle M Epstein5, Andreas Bergthaler2.
Abstract
Immune responses are tightly regulated to ensure efficient pathogen clearance while avoiding tissue damage. Here we report that Setdb2 was the only protein <span class="Chemical">lysine methyltransferase induced during infection with influenza virus. Setdb2 expression depended on signaling via type I interferons, and Setdb2 repressed expression of the gene encoding the neutrophil attractant CXCL1 and other genes that are targets of the transcription factor NF-κB. This coincided with occupancy by Setdb2 at the Cxcl1 promoter, which in the absence of Setdb2 displayed diminished trimethylation of histone H3 Lys9 (H3K9me3). Mice with a hypomorphic gene-trap construct of Setdb2 exhibited increased infiltration of neutrophils during sterile lung inflammation and were less sensitive to bacterial superinfection after infection with influenza virus. This suggested that a Setdb2-mediated regulatory crosstalk between the type I interferons and NF-κB pathways represents an important mechanism for virus-induced susceptibility to bacterial superinfection.Entities:
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Year: 2014 PMID: 25419628 PMCID: PMC4320687 DOI: 10.1038/ni.3046
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606