SYSBIO Centre for Systems Biology Milano, Italy ; Department of Biotechnology and Biosciences, University of Milano-Bicocca Milano, Italy.
Department of Biotechnology and Biosciences, University of Milano-Bicocca Milano, Italy.
Front Physiol. 2014 Jan 21;4:315. doi: 10.3389/fphys.2013.00315. eCollection 2013.
Cell growth and proliferation require a complex series of tight-regulated and well-orchestrated events. Accordingly, proteins governing such events are evolutionary conserved, even among distant organisms. By contrast, it is more singular the case of "core functions" exerted by functional analogous proteins that are not homologous and do not share any kind of structural similarity. This is the case of proteins regulating the G1/S transition in higher eukaryotes-i.e., the retinoblastoma (Rb) tumor suppressor Rb-and budding yeast, i.e., Whi5. The interaction landscape of Rb and Whi5 is quite large, with more than one hundred proteins interacting either genetically or physically with each protein. The Whi5 interactome has been used to construct a concept map of Whi5 function and regulation. Comparison of physical and genetic interactors of Rb and Whi5 allows highlighting a significant core of conserved, common functionalities associated with the interactors indicating that structure and function of the network-rather than individual proteins-are conserved during evolution. A combined bioinformatics and biochemical approach has shown that the whole Whi5 protein is highly disordered, except for a small region containing the protein family signature. The comparison with Whi5 homologs from Saccharomycetales has prompted the hypothesis of a modular organization of structural disorder, with most evolutionary conserved regions alternating with highly variable ones. The finding of a consensus sequence points to the conservation of a specific phosphorylation rhythm along with two disordered sequence motifs, probably acting as phosphorylation-dependent seeds in Whi5 folding/unfolding. Thus, the widely disordered Whi5 appears to act as a hierarchical, "date hub" that has evolutionary assayed an original way of modular organization before being supplanted by the globular, multi-domain structured Rb, more suitable to cover the role of a "party hub".
细胞的生长和增殖需要一系列复杂的、紧密调节和协调的事件。因此,控制这些事件的蛋白质在进化上是保守的,即使在遥远的生物中也是如此。相比之下,功能类似的蛋白质发挥的“核心功能”就更为独特,这些蛋白质不是同源的,也没有任何结构上的相似性。这种情况发生在调节高等真核生物 G1/S 转换的蛋白质中,即视网膜母细胞瘤(Rb)肿瘤抑制因子 Rb 和芽殖酵母,即 Whi5。Rb 和 Whi5 的相互作用景观非常大,有超过一百种蛋白质在遗传或物理上与每种蛋白质相互作用。Whi5 的相互作用组已被用于构建 Whi5 功能和调节的概念图。比较 Rb 和 Whi5 的物理和遗传相互作用体允许突出与相互作用体相关的保守、常见功能的核心,这表明在进化过程中,网络的结构和功能而不是单个蛋白质是保守的。综合生物信息学和生化方法表明,整个 Whi5 蛋白高度无序,除了包含蛋白质家族特征的一小区域外。与 Saccharomycetales 的 Whi5 同源物的比较促使人们提出了结构无序的模块化组织假设,大多数进化上保守的区域与高度可变的区域交替出现。保守序列的发现指向了沿特定磷酸化节律的保守性,以及两个无序序列基序,这两个基序可能在 Whi5 折叠/展开中作为磷酸化依赖性的种子。因此,广泛无序的 Whi5 似乎充当了一个层次化的“日期集线器”,在被球形、多结构域的 Rb 取代之前,它已经进化出了一种原始的模块化组织方式,Rb 更适合扮演“聚会集线器”的角色。