CTCF Mediates the Cis-Regulatory Hubs in Mouse Hearts.
Mick Lee, Loïc Mangnier, Cory C Padilla, Dominic Paul Lee, Wilson Tan, Wen Hao Zheng, Louis Hanqiang Gan, Ching Kit Chen, Yee Phong Lim, Rina Miao Qin Wang, Peter Yiqing Li, Yonglin Zhu, Steve Bilodeau, Alexandre Bureau, Roger Sik-Yin Foo
Abstract
Open AccessThe 3D chromatin architecture establishes a complex network of genes and regulatory elements necessary for transcriptomic regulation in development and disease. This network can be modeled by cis-regulatory hubs (CRH), which underscore the local functional interactions between enhancers and promoter regions and differ from other higher-order chromatin structures such as topologically associated domains (TAD). The activity-by-contact (ABC) model of enhancer-promoter regulation has been recently used in the identification of these CRHs, but little is known about the role of transcription factor CCTC binding factor (CTCF) on ABC scores and their consequent impact on CRHs. Here, we show that the loss of CTCF leads to a reorganization of the ABC-derived rankings of putative enhancers in the mouse heart, a global reduction in the total number of CRHs and an increase in the size of CRHs. Furthermore, CTCF loss leads to a higher percentage of CRHs that cross TAD boundaries. These results provide additional evidence to support the importance of CTCF in forming the regulatory networks necessary for gene regulation.