Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Genome Biol Evol. 2021 Jun 8;13(6). doi: 10.1093/gbe/evab070.
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.
尽管人们普遍认为,在生命之树上丰富的蛋白质进化缓慢,但对于为什么会这样却没有达成共识。在这里,我报告说,在 Lenski 的大肠杆菌长期进化实验(LTEE)的超突变体种群中,丰富的蛋白质进化缓慢。具体来说,在涵盖 LTEE 60000 代的宏基因组时间序列中,每基因观察到的所有突变的密度,与 mRNA 丰度、蛋白质丰度和蛋白质-蛋白质相互作用程度呈显著负相关。非同义突变密度也呈现相同的模式。然而,在 LTEE 超突变体种群中测量的同义突变密度与蛋白质丰度呈正相关。这些结果表明,跨越三个十年实验进化的数据集可以看到对蛋白质进化的普遍限制。因此,应该有可能设计实验来回答为什么丰富的蛋白质进化缓慢。