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Inference of combinatorial regulation in yeast transcriptional networks: a case study of sporulation.

机译:酵母转录网络中组合调控的推论:孢子形成的案例研究。

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Decomposing transcriptional regulatory networks into functional modules and determining logical relations between them is the first step toward understanding transcriptional regulation at the system level. Modules based on analysis of genome-scale data can serve as the basis for inferring combinatorial regulation and for building mathematical models to quantitatively describe the behavior of the networks. We present here an algorithm called modem to identify target genes of a transcription factor (TF) from a single expression experiment, based on a joint probabilistic model for promoter sequence and gene expression data. We show how this method can facilitate the discovery of specific instances of combinatorial regulation and illustrate this for a specific case of transcriptional networks that regulate sporulation in the yeast Saccharomyces cerevisiae. Applying this method to analyze two crucial TFs in sporulation, Ndt80p and Sum1p, we were able to delineate their overlapping binding sites. We proposeda mechanistic model for the competitive regulation by the two TFs on a defined subset of sporulation genes. We show that this model accounts for the temporal control of the "middle" sporulation genes and suggest a similar regulatory arrangement can be found in developmental programs in higher organisms.
机译:将转录调控网络分解为功能模块并确定它们之间的逻辑关系是在系统级别理解转录调控的第一步。基于基因组规模数据分析的模块可以用作推断组合调控和建立数学模型以定量描述网络行为的基础。我们在这里提出一种称为调制解调器的算法,该算法基于启动子序列和基因表达数据的联合概率模型,从单个表达实验中识别转录因子(TF)的目标基因。我们展示了这种方法如何可以促进发现特定的组合调控实例,并针对在酿酒酵母中调控孢子形成的转录网络的特定实例说明了这一点。应用此方法分析孢子形成过程中的两个关键TF,Ndt80p和Sum1p,我们能够描绘出它们重叠的结合位点。我们提出了一种机制模型,用于通过两个TF对孢子基因的定义子集进行竞争调节。我们表明,该模型说明了“中间”孢子形成基因的时间控制,并暗示在高等生物的发育程序中可以发现类似的调控安排。

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