Ancient Hybridisation Fuelled Diversification in Acropora Corals.

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Tianzhen Wu, Alan Ningyuan Xu, Yanli Lei, Haijun Song
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引用次数: 0

Abstract

Introgression is the infiltration or flow of genes from one species to another through hybridisation followed by backcrossing. This may lead to incorrect phylogenetic reconstruction or divergence-time estimation. Acropora is a dominant genus of reef-building corals; however, whether this group has an introgression history before their diversification remains unclear, and previous divergence-time estimates of Acropora have not considered the impact of introgression. In this study, we broke through the limitation of a few genes and a few species and proved the existence of ancient introgression in the evolution of Acropora from whole-genome protein-coding sequences. We inferred 21.9% of all triplet loci (homologous loci from three different species) with a history of introgression and a series of introgression events with a genetic material contribution of up to 30.9% before diversification. Furthermore, 7756 nuclear loci were clustered into three groups using a multidimensional scaling algorithm, the heterogeneity of which resulted in different phylogenetic relationships. The diversification time of Acropora was estimated to be middle to late Miocene when we retained only the gene group with the lowest degree of introgression. The collision of Australia with the Pacific arcs and the Southeast Asian margin in the early Miocene, and a series of cooling events in the middle to late Miocene, may provide geographical and climatic conditions for the diversification of Acropora, respectively. Therefore, our results indicate that at the genome-wide level, ancient introgressive hybridisation may have promoted the radiation evolution of Acropora. Based on our results, the influence of introgression should be taken into account when reconstructing phylogenetic relationships and evaluating divergence time.

古老的杂交促进了 Acropora 珊瑚的多样化。
引入是指一个物种的基因通过杂交或回交渗入或流向另一个物种。这可能会导致不正确的系统发育重建或分歧时间估计。Acropora 是造礁珊瑚中的主要属种;然而,该属种在分化之前是否有引种历史仍不清楚,而且以前对 Acropora 的分化时间估计也没有考虑引种的影响。在这项研究中,我们突破了少数基因和少数物种的限制,从全基因组蛋白质编码序列中证明了Acropora进化过程中存在古老的引种。我们推断出21.9%的三重基因位点(来自三个不同物种的同源基因位点)有引种历史,以及一系列引种事件,其遗传物质贡献率高达30.9%。此外,利用多维缩放算法将 7756 个核位点聚类为三组,其异质性导致了不同的系统发育关系。当我们只保留引入程度最低的基因组时,Acropora 的多样化时间估计为中新世中晚期。中新世早期澳大利亚与太平洋弧和东南亚边缘的碰撞,以及中新世中晚期的一系列降温事件,可能分别为 Acropora 的多样化提供了地理和气候条件。因此,我们的研究结果表明,在全基因组水平上,古老的引种杂交可能促进了银孔藻的辐射演化。基于我们的研究结果,在重建系统发育关系和评估分化时间时,应考虑到引种的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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