CRISPR-Based Editing Reveals Edge-Specific Effects in Biological Networks Conference: Mammalian Synthetic Biology WorkshopYear: 2018Proceeding: Fifth International Mammalian Synthetic Biology Workshop (mSBW 5.0)Group: Poster SessionSession: Poster Session Time: Saturday, May 5, 2018 - 5:30pm-6:30pm Authors: Li, Y., The University of Texas at Dallas Nowak, C., The University of Texas at Dallas Pertsemlidis, A., University of Texas Health Science Center at San Antonio Bleris, L., The University of Texas at Dallas Unraveling the properties of biological networks is central to understanding normal and disease cellular phenotypes. Networks consist of functional elements (nodes) that form a variety of diverse connections (edges) with each node being a hub for multiple edges. Herein, in contrast to node-centric network perturbation and analysis approaches, we present a high-throughput CRISPR-based methodology for delineating the role of network edges. Ablation of network edges using a library targeting 93 miRNA target sites in 71 genes reveals numerous edges that control, with variable importance, cellular survival under stress. To compare the impact of removing nodes versus edges in a biological network, we dissect a specific p53-microRNA pathway. In summary, we demonstrate that network edges are critical to the function and stability of biological networks. Our results introduce a novel genetic screening opportunity via edge ablation and highlight a new dimension in biological network analysis.