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High-throughput and quantitative assessment of enhancer activity in mammals by CapStarr-seq

Author

Listed:
  • Laurent Vanhille

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC)

  • Aurélien Griffon

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC)

  • Muhammad Ahmad Maqbool

    (Institute of Molecular Genetics of Montpellier (IGMM), UMR5535 CNRS)

  • Joaquin Zacarias-Cabeza

    (Institute of Biomedical Research, University of Birmingham)

  • Lan T.M. Dao

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC)

  • Nicolas Fernandez

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC
    TGML, IBiSA platform)

  • Benoit Ballester

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC)

  • Jean Christophe Andrau

    (Institute of Molecular Genetics of Montpellier (IGMM), UMR5535 CNRS)

  • Salvatore Spicuglia

    (Inserm U1090, Technological Advances for Genomics and Clinics (TAGC)
    Aix-Marseille University UMR-S 1090, TAGC)

Abstract

Cell-type specific regulation of gene expression requires the activation of promoters by distal genomic elements defined as enhancers. The identification and the characterization of enhancers are challenging in mammals due to their genome complexity. Here we develop CapStarr-Seq, a novel high-throughput strategy to quantitatively assess enhancer activity in mammals. This approach couples capture of regions of interest to previously developed Starr-seq technique. Extensive assessment of CapStarr-seq demonstrates accurate quantification of enhancer activity. Furthermore, we find that enhancer strength is associated with binding complexity of tissue-specific transcription factors and super-enhancers, while additive enhancer activity isolates key genes involved in cell identity and function. The CapStarr-Seq thus provides a fast and cost-effective approach to assess the activity of potential enhancers for a given cell type and will be helpful in decrypting transcription regulation mechanisms.

Suggested Citation

  • Laurent Vanhille & Aurélien Griffon & Muhammad Ahmad Maqbool & Joaquin Zacarias-Cabeza & Lan T.M. Dao & Nicolas Fernandez & Benoit Ballester & Jean Christophe Andrau & Salvatore Spicuglia, 2015. "High-throughput and quantitative assessment of enhancer activity in mammals by CapStarr-seq," Nature Communications, Nature, vol. 6(1), pages 1-10, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7905
    DOI: 10.1038/ncomms7905
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    Cited by:

    1. 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.

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