Sahlgrenska Cancer Center, University of Gothenburg, Gothenburg, Sweden.
PLoS One. 2013 Jul 25;8(7):e68598. doi: 10.1371/journal.pone.0068598. Print 2013.
Functionally interacting perturbations, such as synergistic drugs pairs or synthetic lethal gene pairs, are of key interest in both pharmacology and functional genomics. However, to find such pairs by traditional screening methods is both time consuming and costly. We present a novel computational-experimental framework for efficient identification of synergistic target pairs, applicable for screening of systems with sizes on the order of current drug, small RNA or SGA (Synthetic Genetic Array) libraries (>1000 targets). This framework exploits the fact that the response of a drug pair in a given system, or a pair of genes' propensity to interact functionally, can be partly predicted by computational means from (i) a small set of experimentally determined target pairs, and (ii) pre-existing data (e.g. gene ontology, PPI) on the similarities between targets. Predictions are obtained by a novel matrix algebraic technique, based on cyclical projections onto convex sets. We demonstrate the efficiency of the proposed method using drug-drug interaction data from seven cancer cell lines and gene-gene interaction data from yeast SGA screens. Our protocol increases the rate of synergism discovery significantly over traditional screening, by up to 7-fold. Our method is easy to implement and could be applied to accelerate pair screening for both animal and microbial systems.
功能相互作用的扰动,如协同药物对或合成致死基因对,在药理学和功能基因组学中都具有重要意义。然而,通过传统的筛选方法找到这样的对既费时又费钱。我们提出了一种新的计算实验框架,用于有效地识别协同靶对,适用于筛选当前药物、小 RNA 或 SGA(合成遗传阵列)文库(>1000 个靶标)大小的系统。该框架利用了这样一个事实,即给定系统中药物对的反应,或一对基因相互作用的功能倾向,可以部分通过计算手段从(i)一小部分实验确定的靶对,和(ii)关于目标之间相似性的预先存在的数据(例如基因本体论、蛋白质-蛋白质相互作用)来预测。预测是通过一种新的基于凸集循环投影的矩阵代数技术获得的。我们使用来自七个癌细胞系的药物-药物相互作用数据和来自酵母 SGA 筛选的基因-基因相互作用数据来证明所提出方法的效率。与传统的筛选方法相比,我们的方案大大提高了协同发现的速度,高达 7 倍。我们的方法易于实施,可用于加速动物和微生物系统的配对筛选。