Department of Gynecologic Oncology, Women's Hospital and Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou 310006, China.
Institute of Bioinformatics, Zhejiang University, Hangzhou 310058, China.
Bioinformatics. 2023 Feb 14;39(2). doi: 10.1093/bioinformatics/btad071.
Mammalian cells can be transcriptionally reprogramed to other cellular phenotypes. Controllability of such complex transitions in transcriptional networks underlying cellular phenotypes is an inherent biological characteristic. This network controllability can be interpreted by operating a few key regulators to guide the transcriptional program from one state to another. Finding the key regulators in the transcriptional program can provide key insights into the network state transition underlying cellular phenotypes.
To address this challenge, here, we proposed to identify the key regulators in the transcriptional co-expression network as a minimum dominating set (MDS) of driver nodes that can fully control the network state transition. Based on the theory of structural controllability, we developed a weighted MDS network model (WMDS.net) to find the driver nodes of differential gene co-expression networks. The weight of WMDS.net integrates the degree of nodes in the network and the significance of gene co-expression difference between two physiological states into the measurement of node controllability of the transcriptional network. To confirm its validity, we applied WMDS.net to the discovery of cancer driver genes in RNA-seq datasets from The Cancer Genome Atlas. WMDS.net is powerful among various cancer datasets and outperformed the other top-tier tools with a better balance between precision and recall.
https://github.com/chaofen123/WMDS.net.
Supplementary data are available at Bioinformatics online.
哺乳动物细胞可以被转录重编程为其他细胞表型。在细胞表型的转录网络中,这种复杂的转录网络转换的可控性是一种固有生物学特性。通过操作几个关键调节剂来引导转录程序从一种状态到另一种状态,可以解释这种网络可控性。在转录程序中找到关键调节剂可以为细胞表型的网络状态转换提供关键见解。
为了解决这一挑战,我们在这里提出将转录共表达网络中的关键调节剂识别为驱动节点的最小支配集(MDS),以充分控制网络状态的转变。基于结构可控性理论,我们开发了一种加权 MDS 网络模型(WMDS.net),用于发现差异基因共表达网络的驱动节点。WMDS.net 的权重将网络节点的度和两个生理状态之间基因共表达差异的显著性纳入转录网络节点可控性的度量中。为了验证其有效性,我们将 WMDS.net 应用于从癌症基因组图谱的 RNA-seq 数据集中发现癌症驱动基因。WMDS.net 在各种癌症数据集中都很强大,并且优于其他顶级工具,在精度和召回率之间取得了更好的平衡。
https://github.com/chaofen123/WMDS.net。
补充数据可在 Bioinformatics 在线获得。