Research School of Chemistry, Australian National University, Canberra, ACT, Australia.
Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Melbourne, VIC, Australia.
Mol Biol Evol. 2021 Jun 25;38(7):2915-2929. doi: 10.1093/molbev/msab081.
Serine protease inhibitors (serpins) are found in all kingdoms of life and play essential roles in multiple physiological processes. Owing to the diversity of the superfamily, phylogenetic analysis is challenging and prokaryotic serpins have been speculated to have been acquired from Metazoa through horizontal gene transfer due to their unexpectedly high homology. Here, we have leveraged a structural alignment of diverse serpins to generate a comprehensive 6,000-sequence phylogeny that encompasses serpins from all kingdoms of life. We show that in addition to a central "hub" of highly conserved serpins, there has been extensive diversification of the superfamily into many novel functional clades. Our analysis indicates that the hub proteins are ancient and are similar because of convergent evolution, rather than the alternative hypothesis of horizontal gene transfer. This work clarifies longstanding questions in the evolution of serpins and provides new directions for research in the field of serpin biology.
丝氨酸蛋白酶抑制剂(serpins)存在于所有生命领域,在多种生理过程中发挥着重要作用。由于超家族的多样性,系统发育分析具有挑战性,并且由于其出乎意料的高同源性,推测原核 serpins 是通过水平基因转移从后生动物中获得的。在这里,我们利用不同 serpins 的结构比对生成了一个包含所有生命领域 serpins 的综合 6000 个序列系统发育。我们表明,除了中心“枢纽”高度保守的 serpins 之外,该超家族还广泛多样化为许多新的功能分支。我们的分析表明,枢纽蛋白是古老的,并且由于趋同进化而相似,而不是水平基因转移的替代假设。这项工作阐明了 serpins 进化中的长期存在的问题,并为 serpin 生物学领域的研究提供了新的方向。