Aburatani Sachiyo
Computational Biology Research Center, National Institute of Advanced Industrial Science and Technology, 2-4-7 Aomi, Koto-ku, Tokyo, 135-0064, Japan.
Gene Regul Syst Bio. 2011;5:75-88. doi: 10.4137/GRSB.S7569. Epub 2011 Nov 10.
Revealing the gene regulatory systems among DNA and proteins in living cells is one of the central aims of systems biology. In this study, I used Structural Equation Modeling (SEM) in combination with stepwise factor analysis to infer the protein-DNA interactions for gene expression control from only gene expression profiles, in the absence of protein information. I applied my approach to infer the causalities within the well-studied serial transcriptional regulation composed of GAL-related genes in yeast. This allowed me to reveal the hierarchy of serial transcriptional regulation, including previously unclear protein-DNA interactions. The validity of the constructed model was demonstrated by comparing the results with previous reports describing the regulation of the transcription factors. Furthermore, the model revealed combinatory regulation by Gal4p and Gal80p. In this study, the target genes were divided into three types: those regulated by one factor and those controlled by a combination of two factors.
揭示活细胞中DNA与蛋白质之间的基因调控系统是系统生物学的核心目标之一。在本研究中,我运用结构方程模型(SEM)结合逐步因子分析,在缺乏蛋白质信息的情况下,仅从基因表达谱推断用于基因表达控制的蛋白质-DNA相互作用。我将我的方法应用于推断酵母中由GAL相关基因组成的、已被充分研究的串联转录调控中的因果关系。这使我能够揭示串联转录调控的层次结构,包括先前不清楚的蛋白质-DNA相互作用。通过将结果与先前描述转录因子调控的报告进行比较,证明了所构建模型的有效性。此外,该模型揭示了Gal4p和Gal80p的组合调控。在本研究中,目标基因被分为三种类型:受一个因子调控的基因和受两个因子组合控制的基因。