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Universal Constraints on Protein Evolution in the Long-Term Evolution Experiment with Escherichia coli

机译:大肠杆菌长期演化实验中蛋白质演化的普遍约束

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摘要

Although it is well known that abundant proteins evolve slowly across the tree of life, there is little consensus for why this is true. Here, I report that abundant proteins evolve slowly in the hypermutator populations of Lenski’s long-term evolution experiment with Escherichia coli (LTEE). Specifically, the density of all observed mutations per gene, as measured in metagenomic time series covering 60,000 generations of the LTEE, significantly anticorrelates with mRNA abundance, protein abundance, and degree of protein–protein interaction. The same pattern holds for nonsynonymous mutation density. However, synonymous mutation density, measured across the LTEE hypermutator populations, positively correlates with protein abundance. These results show that universal constraints on protein evolution are visible in data spanning three decades of experimental evolution. Therefore, it should be possible to design experiments to answer why abundant proteins evolve slowly.
机译:众所周知,丰富的蛋白质在生命之树上缓慢发展,虽然很少有共识,为什么这是真的。在这里,我认为丰富的蛋白质在Lenski的长期演进实验与大肠杆菌(LTEE)的长期演进实验中的高培训群中慢慢地发展。具体地,在覆盖60,000代LTEE的MATAGENOMIC时间序列中测量的所有基因的所有观察到的突变的密度,用mRNA丰度,蛋白质丰度和蛋白质 - 蛋白质相互作用的程度显着逆尿。相同的模式适用于非同义词突变密度。然而,在LTEE高培训犬群中测量的同义突变密度,与蛋白质丰度正相关。这些结果表明,在跨越三十年的实验演化的数据中可以看到对蛋白质进化的普遍约束。因此,应该可以设计实验来回答为什么丰富的蛋白质缓慢进化的原因。

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