原核生物转录调控网络进化的一般趋势。

Genome dynamics Pub Date : 2007-01-01 DOI:10.1159/000107604
M Madan Babu, S Balaji, L Aravind
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引用次数: 21

摘要

生物体内的基因表达受转录因子的调控蛋白控制,转录因子识别并结合特定的核苷酸序列。多年来,关于转录因子与靶基因在多种模式原核生物(如大肠杆菌和枯草芽孢杆菌)中的调控相互作用的研究已经积累了大量的信息。这允许以有向图的形式表示这些信息,这通常被称为转录调控网络。网络表示为我们提供了一个很好的概念框架来理解转录调控的结构,无论是在本地还是在全球组织水平上。一些研究表明,从模式生物推断的转录网络可能近似于无标度拓扑结构,这反过来意味着存在一个相对较小的高度连接的调节组(集线器或全局调节器)。虽然图论原理已被应用于推断这些网络的各种特性,但很少有研究真正调查了不同生物中转录调节网络的进化。利用最近开发的利用各种进化原理的计算方法,我们试图在大范围的原核生物中重建和比较这些网络。这为不同生物在进化过程中网络结构的改变和多样化提供了一些见解。首先,我们观察到靶基因比它们的转录调控基因表现出更高水平的保守性。这反过来表明,同一套功能在不同的生物体中可能受到不同的控制,这对它们的适应性辐射有重要贡献。特别是,在网络结构的局部水平上,生物体特异性的转录网络优化主要是通过修补单个调控相互作用而不是整个规模的重复使用或删除网络基序(局部结构)来进化的。反过来,随着系统发育多样化的进行,这一过程似乎有利于重复趋同到无标度结构,尽管有不同的调节中心。
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General trends in the evolution of prokaryotic transcriptional regulatory networks.

Gene expression in organisms is controlled by regulatory proteins termed transcription factors, which recognize and bind to specific nucleotide sequences. Over the years, considerable information has accumulated on the regulatory interactions between transcription factors and their target genes in various model prokaryotes, such as Escherichia coli and Bacillus subtilis. This has allowed the representation of this information in the form of a directed graph, which is commonly referred to as the transcriptional regulatory network. The network representation provides us with an excellent conceptual framework to understand the structure of the transcriptional regulation, both at local and global levels of organization. Several studies suggest that the transcriptional network inferred from model organisms may be approximated by a scale-free topology, which in turn implies the presence of a relatively small group of highly connected regulators (hubs or global regulators). While the graph theoretical principles have been applied to infer various properties of such networks, there have been few studies that have actually investigated the evolution of the transcriptional regulatory networks across diverse organisms. Using recently developed computational methods that exploit various evolutionary principles, we have attempted to reconstruct and compare these networks across a wide-range of prokaryotes. This has provided several insights on the modification and diversification of network structures of various organisms in course of evolution. Firstly, we observed that target genes show a much higher level of conservation than their transcriptional regulators. This in turn suggested that the same set of functions could be differently controlled across diverse organisms, contributing significantly to their adaptive radiations. In particular, at the local level of network structure, organism-specific optimization of the transcription network has evolved primarily via tinkering of individual regulatory interactions rather than whole scale reuse or deletion of network motifs (local structure). In turn, as phylogenetic diversification proceeds, this process appears to have favored repeated convergence to scale-free-like structures, albeit with different regulatory hubs.

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