Selection Across the Three-Dimensional Structure of Venom Proteins from North American Scolopendromorph Centipedes.

IF 2.1 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Molecular Evolution Pub Date : 2024-08-01 Epub Date: 2024-07-18 DOI:10.1007/s00239-024-10191-y
Schyler A Ellsworth, Rhett M Rautsaw, Micaiah J Ward, Matthew L Holding, Darin R Rokyta
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引用次数: 0

Abstract

Gene duplication followed by nucleotide differentiation is one of the simplest mechanisms to develop new functions for genes. However, the evolutionary processes underlying the divergence of multigene families remain controversial. We used multigene families found within the diversity of toxic proteins in centipede venom to test two hypotheses related to venom evolution: the two-speed mode of venom evolution and the rapid accumulation of variation in exposed residues (RAVER) model. The two-speed mode of venom evolution proposes that different types of selection impact ancient and younger venomous lineages with negative selection being the predominant form in ancient lineages and positive selection being the dominant form in younger lineages. The RAVER hypothesis proposes that, instead of different types of selection acting on different ages of venomous lineages, the different types of selection will selectively contribute to amino acid variation based on whether the residue is exposed to the solvent where it can potentially interact directly with toxin targets. This hypothesis parallels the longstanding understanding of protein evolution that suggests that residues found within the structural or active regions of the protein will be under negative or purifying selection, and residues that do not form part of these areas will be more prone to positive selection. To test these two hypotheses, we compared the venom of 26 centipedes from the order Scolopendromorpha from six currently recognized species from across North America using both transcriptomics and proteomics. We first estimated their phylogenetic relationships and uncovered paraphyly among the genus Scolopendra and evidence for cryptic diversity among currently recognized species. Using our phylogeny, we then characterized the diverse venom components from across the identified clades using a combination of transcriptomics and proteomics. We conducted selection-based analyses in the context of predicted three-dimensional properties of the venom proteins and found support for both hypotheses. Consistent with the two-speed hypothesis, we found a prevalence of negative selection across all proteins. Consistent with the RAVER hypothesis, we found evidence of positive selection on solvent-exposed residues, with structural and less-exposed residues showing stronger signal for negative selection. Through the use of phylogenetics, transcriptomics, proteomics, and selection-based analyses, we were able to describe the evolution of venom from an ancient venomous lineage and support principles of protein evolution that directly relate to multigene family evolution.

Abstract Image

北美蚣类毒液蛋白三维结构的选择。
基因复制后核苷酸分化是开发基因新功能的最简单机制之一。然而,多基因家族分化的进化过程仍存在争议。我们利用蜈蚣毒液中毒性蛋白多样性中发现的多基因家族来检验与毒液进化有关的两种假说:毒液进化的双速模式和暴露残基变异快速积累(RAVER)模式。毒液进化的双速模式假说认为,不同类型的选择会影响古老和年轻的毒系,在古老毒系中,负向选择占主导地位,而在年轻毒系中,正向选择占主导地位。RAVER 假说认为,不同类型的选择作用于不同年龄的毒系,而不同类型的选择将根据残基是否暴露在溶剂中,是否有可能直接与毒素靶标相互作用,选择性地促成氨基酸变异。这一假说与长期以来对蛋白质进化的理解相似,即蛋白质结构或活性区域内的残基将受到负向或纯化选择,而不属于这些区域的残基则更容易受到正向选择。为了验证这两个假设,我们使用转录组学和蛋白质组学方法,比较了北美目前已知的六个物种中 26 种蜈蚣的毒液。我们首先估算了它们的系统发育关系,发现了Scolopendra属之间的旁系关系,以及目前已知物种之间的隐性多样性证据。利用我们的系统发生学,我们结合转录组学和蛋白质组学对已确定支系中的不同毒液成分进行了表征。我们根据预测的毒液蛋白三维特性进行了基于选择的分析,发现两种假说都得到了支持。与双速假说一致的是,我们发现所有蛋白质都普遍存在负选择。与 RAVER 假说一致,我们发现溶剂暴露残基存在正选择的证据,而结构性残基和暴露较少的残基则显示出更强的负选择信号。通过使用系统发生学、转录组学、蛋白质组学和基于选择的分析,我们能够描述一个古老毒系的毒液进化过程,并支持与多基因家族进化直接相关的蛋白质进化原则。
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来源期刊
Journal of Molecular Evolution
Journal of Molecular Evolution 生物-进化生物学
CiteScore
5.50
自引率
2.60%
发文量
36
审稿时长
3 months
期刊介绍: Journal of Molecular Evolution covers experimental, computational, and theoretical work aimed at deciphering features of molecular evolution and the processes bearing on these features, from the initial formation of macromolecular systems through their evolution at the molecular level, the co-evolution of their functions in cellular and organismal systems, and their influence on organismal adaptation, speciation, and ecology. Topics addressed include the evolution of informational macromolecules and their relation to more complex levels of biological organization, including populations and taxa, as well as the molecular basis for the evolution of ecological interactions of species and the use of molecular data to infer fundamental processes in evolutionary ecology. This coverage accommodates such subfields as new genome sequences, comparative structural and functional genomics, population genetics, the molecular evolution of development, the evolution of gene regulation and gene interaction networks, and in vitro evolution of DNA and RNA, molecular evolutionary ecology, and the development of methods and theory that enable molecular evolutionary inference, including but not limited to, phylogenetic methods.
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