Vockley Christopher M, McDowell Ian C, D'Ippolito Antony M, Reddy Timothy E
a Department of Biostatistics & Bioinformatics , Duke University , Durham , NC , USA.
b Center for Genomic & Computational Biology , Duke University , Durham , NC , USA.
Transcription. 2017 Aug 8;8(4):261-267. doi: 10.1080/21541264.2017.1317694. Epub 2017 Jun 9.
Gene regulation is fundamentally important for the coordination of diverse biologic processes including homeostasis and responses to developmental and environmental stimuli. Transcription factor (TF) binding sites are one of the major functional subunits of gene regulation. They are arranged in cis-regulatory modules (CRMs) that can be more active than the sum of their individual effects. Recently, we described a mechanism of glucocorticoid (GC)-induced gene regulation in which the glucocorticoid receptor (GR) binds coordinately to multiple CRMs that are 10s of kilobases apart in the genome. In those results, the minority of GR binding sites appear to involve direct TF:DNA interactions. Meanwhile, other GR binding sites in a cluster interact with those direct binding sites to tune their gene regulatory activity. Here, we consider the implications of those and related results in the context of existing models of gene regulation. Based on our analyses, we propose that the billboard and regulatory grammar models of cis-regulatory element activity be expanded to consider the influence of long-range interactions between cis-regulatory modules.
基因调控对于协调包括内稳态以及对发育和环境刺激的反应在内的多种生物学过程至关重要。转录因子(TF)结合位点是基因调控的主要功能亚基之一。它们排列在顺式调控模块(CRM)中,这些模块的活性可能比其各自效应的总和更高。最近,我们描述了一种糖皮质激素(GC)诱导的基因调控机制,其中糖皮质激素受体(GR)协同结合到基因组中相距数十千碱基的多个CRM上。在这些结果中,少数GR结合位点似乎涉及直接的TF:DNA相互作用。同时,簇中的其他GR结合位点与那些直接结合位点相互作用,以调节它们的基因调控活性。在这里,我们在现有基因调控模型的背景下考虑这些及相关结果的意义。基于我们的分析,我们建议扩展顺式调控元件活性的广告牌和调控语法模型,以考虑顺式调控模块之间长程相互作用的影响。