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arXiv 2403.09436q-bio.BMcond-mat.dis-nnq-bio.PE
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蛋白质进化中上位效应的涌现时间尺度

Emergent time scales of epistasis in protein evolution

Leonardo Di Bari, Matteo Bisardi, Sabrina Cotogno, Martin Weigt, Francesco Zamponi

AI总结:

提出数据驱动的蛋白质进化上位效应模型,通过适应度景观模拟进化,准确再现多时间尺度序列统计,揭示上位效应集体性质,定量再现偶然性、固化及可预测性丧失现象,挑战独立位点模型。

摘要:

我们引入了一种数据驱动的蛋白质进化上位效应模型,能够生成跨越从单个突变到分化同源蛋白等截然不同时间尺度的进化轨迹。我们的计算机模拟进化包含随机核苷酸突变、插入和缺失,并使用适应度景观对选择进行建模,该景观通过蛋白质家族的生成概率模型推断得出。我们表明,所提出的框架准确再现了短时间(实验性)和长时间(自然)蛋白质进化的序列统计特征,表明其也适用于目前进化实验无法触及的、数据相对匮乏的中间进化时间尺度。我们的模型揭示了上位效应的高度集体性质,即在分化的序列背景下逐渐改变突变的适应度效应,而不是通过单个突变间的强相互作用起作用。这种集体性质触发了长时间进化尺度的涌现,将给定序列背景内的快速突变过程与背景本身的缓慢进化分离开来。该模型定量再现了偶然性和固化等上位效应现象,以及在远缘同源蛋白的深度突变扫描实验中观察到的蛋白质进化可预测性丧失现象。它从而加深了我们对突变与选择在塑造蛋白质多样性和新功能中相互作用的理解,允许对进化进行统计预测,并挑战了当前主流的蛋白质进化独立位点模型,这些模型无法捕捉上位效应的根本重要性。

英文摘要:

We introduce a data-driven epistatic model of protein evolution, capable of generating evolutionary trajectories spanning very different time scales reaching from individual mutations to diverged homologs. Our in silico evolution encompasses random nucleotide mutations, insertions and deletions, and models selection using a fitness landscape, which is inferred via a generative probabilistic model for protein families. We show that the proposed framework accurately reproduces the sequence statistics of both short-time (experimental) and long-time (natural) protein evolution, suggesting applicability also to relatively data-poor intermediate evolutionary time scales, which are currently inaccessible to evolution experiments. Our model uncovers a highly collective nature of epistasis, gradually changing the fitness effect of mutations in a diverging sequence context, rather than acting via strong interactions between individual mutations. This collective nature triggers the emergence of a long evolutionary time scale, separating fast mutational processes inside a given sequence context, from the slow evolution of the context itself. The model quantitatively reproduces epistatic phenomena such as contingency and entrenchment, as well as the loss of predictability in protein evolution observed in deep mutational scanning experiments of distant homologs. It thereby deepens our understanding of the interplay between mutation and selection in shaping protein diversity and novel functions, allows one to statistically forecast evolution, and challenges the prevailing independent-site models of protein evolution, which are unable to capture the fundamental importance of epistasis.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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