A regulatory module driving the recurrent evolution of irreducible molecular complexes.

Polina Tikanova, James Julian Ross, Andreas Hagmueller, Florian Puehringer, Pinelopi Pliota, Daniel Krogull, Valeria Stefania, Manuel Hunold, Alevtina Koreshova, Anja Koller, Ivanna Ostapchuk, Jacqueline Okweri, Joseph Gokcezade, Peter Duchek, Gang Dong, Eyal Ben-David, Alejandro Burga
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Abstract

To sustain life, molecular complexes require the concerted action of multiple proteins, each relying on one another to perform intricate tasks. However, how such interdependent protein interactions evolve in the first place is poorly understood. To address this, we investigated the origins of a group of fast-evolving genetic parasites, toxin-antidote elements, which boil down this dilemma to a simple question: what came first, the toxin or the antidote? By integrating quantitative genetics, biochemistry, and evolutionary genomics, we discovered that toxins and antidotes can arise simultaneously through the duplication of a regulatory module comprising an F-box protein in linkage to its substrate. Our findings provide one solution to the recurrent emergence of mutual dependence in protein complexes and illustrate in detail how complexity can swiftly arise from simplicity.
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驱动不可还原分子复合物反复进化的调控模块。
为了维持生命,分子复合体需要多种蛋白质的协同作用,每种蛋白质都依赖彼此来执行复杂的任务。然而,人们对这种相互依赖的蛋白质相互作用最初是如何进化的却知之甚少。为了解决这个问题,我们研究了一组快速进化的遗传寄生虫--毒素-解毒元素的起源,它们将这一难题归结为一个简单的问题:先有毒素还是先有解毒剂?通过整合定量遗传学、生物化学和进化基因组学,我们发现毒素和解毒剂可以通过一个由 F-box 蛋白与其底物连接组成的调控模块的复制而同时产生。我们的发现为蛋白质复合物中反复出现的相互依赖关系提供了一种解决方案,并详细说明了复杂性是如何从简单性中迅速产生的。
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