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Targeting c-Myc-activated genes with a correlation method: Detection of global changes in large gene expression network dynamics

机译:使用相关方法靶向c-Myc激活的基因:检测大型基因表达网络动力学的全局变化

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摘要

This work studies the dynamics of a gene expression time series network. The network, which is obtained from the correlation of gene expressions, exhibits global dynamic properties that emerge after a cell state perturbation. The main features of this network appear to be more robust when compared with those obtained with a network obtained from a linear Markov model. In particular, the network properties strongly depend on the exact time sequence relationships between genes and are destroyed by random temporal data shuffling. We discuss in detail the problem of finding targets of the c-myc protooncogene, which encodes a transcriptional regulator whose inappropriate expression has been correlated with a wide array of malignancies. The data used for network construction are a time series of gene expression, collected by microarray analysis of a rat fibroblast cell line expressing a conditional Myc-estrogen receptor oncoprotein. We show that the correlation-based model can establish a clear relationship between network structure and the cascade of c-myc-activated genes.
机译:这项工作研究了基因表达时间序列网络的动力学。从基因表达的相关性获得的网络展现出在细胞状态扰动后出现的全局动态特性。与使用线性马尔可夫模型获得的网络相比,该网络的主要特征似乎更健壮。特别是,网络属性在很大程度上取决于基因之间的确切时间序列关系,并且会被随机的时间数据混洗破坏。我们将详细讨论寻找c-myc原癌基因靶标的问题,该靶标编码的转录调控因子的不适当表达与多种恶性肿瘤有关。用于网络构建的数据是基因表达的时间序列,通过表达条件性Myc-雌激素受体癌蛋白的大鼠成纤维细胞系的微阵列分析收集。我们表明基于相关的模型可以建立网络结构和c-myc激活基因的级联之间的明确关系。

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