超越基因流动:一对高度分化的同胞物种中次级接触的(非)平行性。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Pub Date : 2024-08-09 DOI:10.1111/mec.17488
Hannah Augustijnen, Kay Lucek
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引用次数: 0

摘要

复制的次生接触区可以让我们深入了解物种演化过程中基因流动的重要障碍,并揭示次生接触在多大程度上可能导致类似的进化结果。在这里,我们利用全基因组重测序数据研究了高山蝴蝶属(Erebia)高度分化的两个次级接触区。我们评估了种群和物种之间的基因组关系,发现杂交非常罕见,在这两个接触区都没有或几乎没有当前或历史上的引种。接触区之间有很大的相似性,这与种间分化的同域起源一致,没有迹象表明存在持续的强化选择。与预期的有效种群数量减少相一致,我们进一步发现,与整个基因组的高分化水平相比,与 Z 染色体相关的支架显示出更高的分化水平,这也暗示了 Z 染色体对该系统中物种分化的贡献。最后,我们在所有的卡西欧蝶(E. cassioides)中都检测到了内共生体沃尔巴克氏体(Wolbachia)的存在,这种内共生体可导致宿主之间的生殖隔离,而在接触区的滇滇蝶种群中似乎完全或基本不存在这种内共生体。我们将讨论这种罕见的模式是如何产生的,以及它是如何影响物种在二次接触时的动态演化的。
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Beyond gene flow: (non)-parallelism of secondary contact in a pair of highly differentiated sibling species

Replicated secondary contact zones can provide insights into the barriers to gene flow that are important during speciation and can reveal to which degree secondary contact may result in similar evolutionary outcomes. Here, we studied two secondary contact zones between highly differentiated Alpine butterflies of the genus Erebia using whole-genome resequencing data. We assessed the genomic relationships between populations and species and found hybridization to be rare, with no to little current or historical introgression in either contact zone. There are large similarities between contact zones, consistent with an allopatric origin of interspecific differentiation, with no indications for ongoing reinforcing selection. Consistent with expected reduced effective population size, we further find that scaffolds related to the Z-chromosome show increased differentiation compared to the already high levels across the entire genome, which could also hint towards a contribution of the Z chromosome to species divergence in this system. Finally, we detected the presence of the endosymbiont Wolbachia, which can cause reproductive isolation between its hosts, in all E. cassioides, while it appears to be fully or largely absent in contact zone populations of E. tyndarus. We discuss how this rare pattern may have arisen and how it may have affected the dynamics of speciation upon secondary contact.

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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
期刊最新文献
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