重构基因调控网络:从随机到无标度连接。

J Wildenhain, E J Crampin
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引用次数: 30

摘要

利用基因敲除、RNAi和药物相互作用实验的组合来操纵生物体,可以用来揭示基因之间的调节相互作用。已经提出了几种算法,试图从这些实验产生的基因表达数据集重建潜在的调控网络。通常,这些方法假设每个基因在网络中有大约相同数量的相互作用,这些方法依赖于先验知识,或者研究者对平均网络连通性的最佳猜测。然而,最近的证据指出了生物网络中的无标度特性,其中网络连接遵循幂律分布。对于无标度网络,每个基因的调节相互作用的平均数量不能令人满意地表征网络。考虑到这一点,本文介绍了一种新的逆向工程方法,该方法不需要预先了解网络连接,并使用具有生物学相关网络结构的模拟基因表达数据与其他已发表的算法进行了性能比较。由于该方法不需要对网络连接的分布作任何假设,因此适用于无标度网络。
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Reconstructing gene regulatory networks: from random to scale-free connectivity.

The manipulation of organisms using combinations of gene knockout, RNAi and drug interaction experiments can be used to reveal regulatory interactions between genes. Several algorithms have been proposed that try to reconstruct the underlying regulatory networks from gene expression data sets arising from such experiments. Often these approaches assume that each gene has approximately the same number of interactions within the network, and the methods rely on prior knowledge, or the investigator's best guess, of the average network connectivity. Recent evidence points to scale-free properties in biological networks, however, where network connectivity follows a power-law distribution. For scale-free networks, the average number of regulatory interactions per gene does not satisfactorily characterise the network. With this in mind, a new reverse engineering approach is introduced that does not require prior knowledge of network connectivity and its performance is compared with other published algorithms using simulated gene expression data with biologically relevant network structures. Because this new approach does not make any assumptions about the distribution of network connections, it is suitable for application to scale-free networks.

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