Do protein language models learn phylogeny?

IF 7.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Briefings in bioinformatics Pub Date : 2024-11-22 DOI:10.1093/bib/bbaf047
Sanjana Tule, Gabriel Foley, Mikael Bodén
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Abstract

Deep machine learning demonstrates a capacity to uncover evolutionary relationships directly from protein sequences, in effect internalising notions inherent to classical phylogenetic tree inference. We connect these two paradigms by assessing the capacity of protein-based language models (pLMs) to discern phylogenetic relationships without being explicitly trained to do so. We evaluate ESM2, ProtTrans, and MSA-Transformer relative to classical phylogenetic methods, while also considering sequence insertions and deletions (indels) across 114 Pfam datasets. The largest ESM2 model tends to outperform other pLMs (including the multimodal ESM3) by recovering phylogenetic relationships among homologous protein sequences in both low- and high-gap settings. pLMs agree with conventional phylogenetic methods in general, but more so for protein families with fewer implied indels, highlighting indels as a key factor differentiating classical phylogenetics from pLMs. We find that pLMs preferentially capture broader as opposed to finer evolutionary relationships within a specific protein family, where ESM2 has a sweet spot for highly divergent sequences, at remote distance. Less than 10% of neurons are sufficient to broadly recapitulate classical phylogenetic distances; when used in isolation, the difference between the paradigms is further diminished. We show these neurons are polysemantic, shared among different homologous families but never fully overlapping. We highlight the potential of ESM2 as a complementary tool for phylogenetic analysis, especially when extending to remote homologs that are difficult to align and imply complex histories of insertions and deletions. Implementations of analyses are available at https://github.com/santule/pLMEvo.

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蛋白质语言模型学习系统发育吗?
深度机器学习展示了直接从蛋白质序列中发现进化关系的能力,实际上内化了经典系统发育树推理固有的概念。我们通过评估基于蛋白质的语言模型(pLMs)在没有明确训练的情况下识别系统发育关系的能力,将这两种范式联系起来。我们评估了ESM2、ProtTrans和MSA-Transformer相对于经典的系统发育方法,同时也考虑了114个Pfam数据集的序列插入和缺失(indels)。最大的ESM2模型往往优于其他pLMs(包括多模态ESM3),通过恢复同源蛋白序列在低间隙和高间隙设置中的系统发育关系。一般来说,plm与传统的系统发育方法一致,但对于含有较少隐含索引的蛋白质家族则更一致,这突出了索引是区分经典系统发育与plm的关键因素。我们发现pLMs优先捕获更广泛的,而不是特定蛋白质家族中更精细的进化关系,其中ESM2在远距离上具有高度分化序列的最佳点。不到10%的神经元足以概括经典的系统发育距离;当单独使用时,范式之间的差异进一步缩小。我们发现这些神经元是多义的,在不同的同源家族中共享,但从未完全重叠。我们强调了ESM2作为系统发育分析的补充工具的潜力,特别是当扩展到难以校准和暗示插入和删除的复杂历史的远程同源物时。分析的实现可以在https://github.com/santule/pLMEvo上找到。
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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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