Liu Li, Zhang Li-Rong, Dao Fu-Ying, Yang Yan-Chao, Lin Hao
Laboratory of Theoretical Biophysics, School of Physical Science and Technology, Inner Mongolia University, Hohhot 010021, China.
School of Life Science and Technology, Center for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Mol Ther Nucleic Acids. 2020 Nov 17;23:347-354. doi: 10.1016/j.omtn.2020.11.011. eCollection 2021 Mar 5.
The pairwise interaction between transcription factors (TFs) plays an important role in enhancer-promoter loop formation. Although thousands of TFs in the human genome have been found, only a few TF pairs have been demonstrated to be related to loop formation. It is still a challenge to determine which TF pairs could be involved in the enhancer-promoter regulation network. This work describes a computational framework to identify TF pairs in enhancer-promoter regulation. By integrating different levels of data derived from Promoter Capture Hi-C, chromatin immunoprecipitation sequencing (ChIP-seq) of histone marks, RNA-seq, protein-protein interaction (PPI), and TF motif, we identified 361 significant TF pairs and constructed a TF interaction network. From the network, we found several hub-TFs, which may have important roles in the regulation of long-range interactions. Our studies extended TF pairs identified in other experimental and computational approaches. These findings will help the further study of long-range interactions between enhancers and promoters.
转录因子(TFs)之间的成对相互作用在增强子 - 启动子环形成中起着重要作用。尽管在人类基因组中已发现数千种转录因子,但仅有少数转录因子对被证明与环形成有关。确定哪些转录因子对可能参与增强子 - 启动子调控网络仍然是一项挑战。这项工作描述了一种用于识别增强子 - 启动子调控中转录因子对的计算框架。通过整合来自启动子捕获Hi-C、组蛋白标记的染色质免疫沉淀测序(ChIP-seq)、RNA测序、蛋白质 - 蛋白质相互作用(PPI)和转录因子基序的不同层次数据,我们识别出361个显著的转录因子对并构建了一个转录因子相互作用网络。从该网络中,我们发现了几个枢纽转录因子,它们可能在远程相互作用的调控中发挥重要作用。我们的研究扩展了在其他实验和计算方法中识别出的转录因子对。这些发现将有助于进一步研究增强子和启动子之间的远程相互作用。