大堡礁上的珊瑚 Acropora kenti 染色体倒位蕴藏着过多的突变负荷。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jia Zhang, Nadja M. Schneller, Matt A. Field, Cheong Xin Chan, David J. Miller, Jan M. Strugnell, Cynthia Riginos, Line Bay, Ira Cooke
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引用次数: 0

摘要

随着海洋变暖和极端天气事件日益频繁,人类世界中珊瑚礁未来的生存取决于珊瑚的适应能力。然而,迄今为止,绘制珊瑚基因组变异图的工作几乎都集中在 SNPs 上,忽略了结构变异,而这些结构变异已被证明能驱动其他类群的适应过程。在这里,我们发现造礁珊瑚 Acropora kenti 至少存在五种大型、高度多态的结构变异,所有这些变异都显示出异核型中重组被强烈抑制的特征,而这通常与染色体倒位有关。基于其较高的小等位基因频率、在不同生境中的均匀分布以及较高的遗传负荷,我们认为 A. kenti 中的这些倒位变体很可能处于平衡选择之下。这些位点中对蛋白编码基因影响较大的 SNPs 过多,使其成为适应性选择的潜在目标,并在未来珊瑚种群变得支离破碎或近亲繁殖时成为基因衰退的促成因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chromosomal inversions harbour excess mutational load in the coral, Acropora kenti, on the Great Barrier Reef

Chromosomal inversions harbour excess mutational load in the coral, Acropora kenti, on the Great Barrier Reef

The future survival of coral reefs in the Anthropocene depends on the capacity of corals to adapt as oceans warm and extreme weather events become more frequent. Targeted interventions designed to assist evolutionary processes in corals require a comprehensive understanding of the distribution and structure of standing variation, however, efforts to map genomic variation in corals have so far focussed almost exclusively on SNPs, overlooking structural variants that have been shown to drive adaptive processes in other taxa. Here, we show that the reef-building coral, Acropora kenti, harbours at least five large, highly polymorphic structural variants, all of which exhibit signatures of strongly suppressed recombination in heterokaryotypes, a feature commonly associated with chromosomal inversions. Based on their high minor allele frequency, uniform distribution across habitats and elevated genetic load, we propose that these inversions in A. kenti are likely to be under balancing selection. An excess of SNPs with high impact on protein-coding genes within these loci elevates their importance both as potential targets for adaptive selection and as contributors to genetic decline if coral populations become fragmented or inbred in future.

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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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