McCord Rachel Patton, Berger Michael F, Philippakis Anthony A, Bulyk Martha L
Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Mol Syst Biol. 2007;3:100. doi: 10.1038/msb4100140. Epub 2007 Apr 17.
Numerous genomic and proteomic datasets are permitting the elucidation of transcriptional regulatory networks in the yeast Saccharomyces cerevisiae. However, predicting the condition dependence of regulatory network interactions has been challenging, because most protein-DNA interactions identified in vivo are from assays performed in one or a few cellular states. Here, we present a novel method to predict the condition-specific functions of S. cerevisiae transcription factors (TFs) by integrating 1327 microarray gene expression data sets and either comprehensive TF binding site data from protein binding microarrays (PBMs) or in silico motif data. Importantly, our method does not impose arbitrary thresholds for calling target regions 'bound' or genes 'differentially expressed', but rather allows all the information derived from a TF binding or gene expression experiment to be considered. We show that this method can identify environmental, physical, and genetic interactions, as well as distinct sets of genes that might be activated or repressed by a single TF under particular conditions. This approach can be used to suggest conditions for directed in vivo experimentation and to predict TF function.
大量的基因组和蛋白质组数据集有助于阐明酿酒酵母中的转录调控网络。然而,预测调控网络相互作用的条件依赖性一直具有挑战性,因为体内鉴定出的大多数蛋白质 - DNA 相互作用来自于在一种或几种细胞状态下进行的实验。在这里,我们提出了一种新方法,通过整合 1327 个微阵列基因表达数据集以及来自蛋白质结合微阵列(PBM)的全面转录因子结合位点数据或计算机模拟基序数据,来预测酿酒酵母转录因子(TF)的条件特异性功能。重要的是,我们的方法不会为判定目标区域“被结合”或基因“差异表达”设置任意阈值,而是允许考虑来自转录因子结合或基因表达实验的所有信息。我们表明,该方法可以识别环境、物理和遗传相互作用,以及在特定条件下可能被单个转录因子激活或抑制的不同基因集。这种方法可用于为体内定向实验提供条件建议并预测转录因子功能。