Lee Seungha Alisa, Kristjánsdóttir Katla, Kwak Hojoong
Cornell University.
Res Sq. 2023 Feb 28:rs.3.rs-2592357. doi: 10.21203/rs.3.rs-2592357/v1.
Enhancer RNAs (eRNAs) are non-coding RNAs produced from transcriptional enhancers that are highly correlated with their activities. Using capped nascent RNA sequencing (PRO-cap) dataset in human lymphoblastoid cell lines across individuals, we identified inter-individual variation of expression in over 80 thousand transcribed transcriptional regulatory elements (tTREs), in both enhancers and promoters. Co-expression analysis of eRNAs from tTREs across individuals revealed how enhancers interact with each other and with promoters. Mid-to-long range interactions showed distance-dependent decay, which was modified by TF occupancy. In particular, we found a class of 'bivalent' TFs, including Cohesin, which both facilitates and insulates the interaction between enhancers and/or promoters depending on the topology. In short ranges, we observed strand specific interactions between nearby eRNAs in both convergent or divergent orientations. Our finding supports a cooperative convergent eRNA model, which is compatible with eRNA remodeling neighboring enhancers rather than interfering with each other. Therefore, our approach to infer functional interactions from co-expression analyses provided novel insights into the principles of enhancer interactions depending on the distance, orientation, and the binding landscapes of TFs.
增强子RNA(eRNA)是由转录增强子产生的非编码RNA,与增强子的活性高度相关。利用来自不同个体的人类淋巴母细胞系中的加帽新生RNA测序(PRO-cap)数据集,我们在增强子和启动子中鉴定出超过8万个转录调控元件(tTRE)的个体间表达差异。对不同个体tTRE的eRNA进行共表达分析,揭示了增强子之间以及增强子与启动子之间的相互作用方式。中到长距离的相互作用呈现出距离依赖性衰减,这种衰减会受到转录因子(TF)占据情况的影响。特别是,我们发现了一类“双价”转录因子,包括黏连蛋白,它们根据拓扑结构既促进又隔离增强子和/或启动子之间的相互作用。在短距离内,我们观察到在同向或反向排列的相邻eRNA之间存在链特异性相互作用。我们的发现支持一种协同同向eRNA模型,该模型与eRNA重塑相邻增强子而非相互干扰相一致。因此,我们从共表达分析中推断功能相互作用的方法为基于距离、方向和转录因子结合图谱的增强子相互作用原理提供了新的见解。