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Epromoters function as a hub to recruit key transcription factors required for the inflammatory response

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Listed:
  • David Santiago-Algarra

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Charbel Souaid

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Himanshu Singh

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Lan T. M. Dao

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer
    Vinmec Healthcare System)

  • Saadat Hussain

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Alejandra Medina-Rivera

    (Laboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México)

  • Lucia Ramirez-Navarro

    (Laboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México)

  • Jaime A. Castro-Mondragon

    (Aix-Marseille University, INSERM, TAGC
    University of Oslo)

  • Nori Sadouni

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Guillaume Charbonnier

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

  • Salvatore Spicuglia

    (Aix-Marseille University, INSERM, TAGC
    Equipe Labellisée Ligue Contre le Cancer)

Abstract

Gene expression is controlled by the involvement of gene-proximal (promoters) and distal (enhancers) regulatory elements. Our previous results demonstrated that a subset of gene promoters, termed Epromoters, work as bona fide enhancers and regulate distal gene expression. Here, we hypothesized that Epromoters play a key role in the coordination of rapid gene induction during the inflammatory response. Using a high-throughput reporter assay we explored the function of Epromoters in response to type I interferon. We find that clusters of IFNa-induced genes are frequently associated with Epromoters and that these regulatory elements preferentially recruit the STAT1/2 and IRF transcription factors and distally regulate the activation of interferon-response genes. Consistently, we identified and validated the involvement of Epromoter-containing clusters in the regulation of LPS-stimulated macrophages. Our findings suggest that Epromoters function as a local hub recruiting the key TFs required for coordinated regulation of gene clusters during the inflammatory response.

Suggested Citation

  • David Santiago-Algarra & Charbel Souaid & Himanshu Singh & Lan T. M. Dao & Saadat Hussain & Alejandra Medina-Rivera & Lucia Ramirez-Navarro & Jaime A. Castro-Mondragon & Nori Sadouni & Guillaume Charb, 2021. "Epromoters function as a hub to recruit key transcription factors required for the inflammatory response," Nature Communications, Nature, vol. 12(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26861-0
    DOI: 10.1038/s41467-021-26861-0
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    References listed on IDEAS

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    1. Fulai Jin & Yan Li & Jesse R. Dixon & Siddarth Selvaraj & Zhen Ye & Ah Young Lee & Chia-An Yen & Anthony D. Schmitt & Celso A. Espinoza & Bing Ren, 2013. "A high-resolution map of the three-dimensional chromatin interactome in human cells," Nature, Nature, vol. 503(7475), pages 290-294, November.
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    3. Francesco N. Carelli & Angélica Liechti & Jean Halbert & Maria Warnefors & Henrik Kaessmann, 2018. "Repurposing of promoters and enhancers during mammalian evolution," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
    4. Xinchen Wang & Liang He & Sarah M. Goggin & Alham Saadat & Li Wang & Nasa Sinnott-Armstrong & Melina Claussnitzer & Manolis Kellis, 2018. "High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
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    1. Hye Kyung Lee & Michaela Willi & Chengyu Liu & Lothar Hennighausen, 2023. "Cell-specific and shared regulatory elements control a multigene locus active in mammary and salivary glands," Nature Communications, Nature, vol. 14(1), pages 1-17, December.

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