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. 2011 Oct;7(10):e1002165.
doi: 10.1371/journal.ppat.1002165. Epub 2011 Oct 13.

Defining emerging roles for NF-κB in antivirus responses: revisiting the interferon-β enhanceosome paradigm

Affiliations

Defining emerging roles for NF-κB in antivirus responses: revisiting the interferon-β enhanceosome paradigm

Siddharth Balachandran et al. PLoS Pathog. 2011 Oct.
No abstract available

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Temporally distinct roles for NF-κB in antivirus innate immune responses.
(A) In uninfected cells, NF-κB cycles robustly through the nucleus to maintain constitutive expression of basal ifnβ and sustain sutocrine IFN-β signaling. (B) Early in an infection, NF-κB cooperates with ATF-2/c-Jun and IRF-3 to recruit the transcription co-activator CBP/p300 to the ifnβ enhancer. (C) Later in an infection, IRF-3/7 powers expression of ifnβ, and NF-κB is rendered redundant in the ifnβ enhanceosome. (D) NF-κB then switches to regulating a distinct subset of non-IFN genes, including those involved in inflammation and cell survival. The relative importance of each transcription factor in driving gene expression during a particular stage of the immune response is indicated by the intensity of its color, with darker shades representing essential functions, and lighter shades indicating reduced roles.

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