Organizing combinatorial transcription factor recruitment at cis-regulatory modules

Transcription. 2018;9(4):233-239. doi: 10.1080/21541264.2017.1394424. Epub 2017 Nov 28.

Abstract

Gene transcriptional regulation relies on cis-regulatory DNA modules (CRMs), which serve as nexus sites for integration of multiple transcription factor (TF) activities. Here, we provide evidence and discuss recent literature indicating that TF recruitment to CRMs is organized into combinations of trans-regulatory protein modules (TRMs). We propose that TRMs are functional entities composed of TFs displaying the most highly interdependent chromatin binding which are, in addition, able to modulate their recruitment to CRMs through inter-TRM effects. These findings shed light on the architectural organization of TF recruitment encoded by their recognition motifs within CRMs.

Keywords: Chromatin binding; DNA recognition elements; cis-regulatory modules; functional genomics; liver; single nucleotide variants; trans-regulatory modules; transcription factors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • DNA / genetics
  • DNA / metabolism
  • Gene Expression Regulation / genetics*
  • Humans
  • Regulatory Elements, Transcriptional / genetics*
  • Transcription Factors / metabolism*

Substances

  • Transcription Factors
  • DNA

Grants and funding

This work was supported by grants from the Fondation pour la Recherche Médicale (Equipe labellisée, DEQ20150331724), “European Genomic Institute for Diabetes” (E.G.I.D., ANR-10-LABX-46) and European Commission. B.S. is supported by the European Research Council (ERC Grant Immunobile, contract 694717).