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Extending the Evolvability Model to the Prokaryotic World: Simulations and Results on Real Data

机译:将进化模型扩展到原核世界:真实数据的模拟和结果

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In 2006, Valiant introduced a variation to his celebrated PAC model to Biology, by which he wished to explain how such complex life mechanisms evolved in that short time by two simple mechanisms - random variation and natural selection. Soon after, several works extended and specialized his work to more specific processes. To the best of our knowledge, there is no such extension to the prokaryotic world, in which gene sharing is the prevailing mode of evolution. Here we extend the evolvability framework to accommodate horizontal gene transfer (HGT), the transfer of genetic material between unrelated organisms. While in a separate work we focused on the theoretical aspects of this extension and its learnability power, here the focus is on more practical and biological facets of this new model. Specifically, we focus on the evolutionary process of developing a trait and model it as the conjunction function. We demonstrate the speedup in learning time for a variant of conjunction to which learning algorithms are known. We also confront the new model with the recombination model on real data of E. coli strains under the task of developing pathogenicity and obtain results adhering to current existing knowledge. Apart from the sheer extension to the understudied prokaryotic world, our work offers comparisons of three different models of evolution under the same conditions, which we believe is unique and of a separate interest.
机译:2006年,Valiant向他著名的PAC模型Biology引入了一种变异,他希望通过两种简单的机制-随机变异和自然选择来解释这种复杂的生命机制在短时间内如何演变。此后不久,几件作品将他的工作扩展到了更具体的过程。就我们所知,原核世界还没有这样的扩展,其中基因共享是主要的进化模式。在这里,我们扩展了可进化性框架,以适应水平基因转移(HGT),即不相关生物之间遗传物质的转移。在单独的工作中,我们专注于此扩展的理论方面及其可学习性,而此处的重点是此新模型的更多实用性和生物学性。具体来说,我们专注于发展特质的进化过程并将其建模为连接函数。我们证明了学习算法已知的一种连接变体的学习时间加快。在发展致病性的任务下,我们还对大肠杆菌菌株的真实数据进行了重组模型对付新模型,并获得了符合现有知识的结果。除了将范围扩展到尚未充分研究的原核生物世界之外,我们的工作还提供了在相同条件下对三种不同进化模型的比较,我们认为这是独一无二的,并且具有不同的利益。

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