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NF-κB dynamics determine the stimulus specificity of epigenomic reprogramming in macrophages.
Cheng, Quen J; Ohta, Sho; Sheu, Katherine M; Spreafico, Roberto; Adelaja, Adewunmi; Taylor, Brooks; Hoffmann, Alexander.
Afiliación
  • Cheng QJ; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
  • Ohta S; Division of Infectious, Diseases Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
  • Sheu KM; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
  • Spreafico R; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
  • Adelaja A; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
  • Taylor B; Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, CA 90095, USA.
  • Hoffmann A; Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
Science ; 372(6548): 1349-1353, 2021 06 18.
Article en En | MEDLINE | ID: mdl-34140389
The epigenome of macrophages can be reprogrammed by extracellular cues, but the extent to which different stimuli achieve this is unclear. Nuclear factor κB (NF-κB) is a transcription factor that is activated by all pathogen-associated stimuli and can reprogram the epigenome by activating latent enhancers. However, we show that NF-κB does so only in response to a subset of stimuli. This stimulus specificity depends on the temporal dynamics of NF-κB activity, in particular whether it is oscillatory or non-oscillatory. Non-oscillatory NF-κB opens chromatin by sustained disruption of nucleosomal histone-DNA interactions, enabling activation of latent enhancers that modulate expression of immune response genes. Thus, temporal dynamics can determine a transcription factor's capacity to reprogram the epigenome in a stimulus-specific manner.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: FN-kappa B / Factor de Transcripción ReIA / Epigenoma / Macrófagos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Science Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: FN-kappa B / Factor de Transcripción ReIA / Epigenoma / Macrófagos Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Science Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos