| Literature DB >> 29105538 |
Julie Dubois-Chevalier1, Parisa Mazrooei2, Mathieu Lupien2, Bart Staels1, Philippe Lefebvre1, Jérôme Eeckhoute1.
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
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Year: 2017 PMID: 29105538 PMCID: PMC6104691 DOI: 10.1080/21541264.2017.1394424
Source DB: PubMed Journal: Transcription ISSN: 2154-1272