尽管存在基因流,但对季节性繁殖的适应和环境相关因素推动了西北大西洋鲱鱼的时空分化

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Angela P. Fuentes-Pardo, Ryan Stanley, Christina Bourne, Rabindra Singh, Kim Emond, Lisa Pinkham, Jenni L. McDermid, Leif Andersson, Daniel E. Ruzzante
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引用次数: 0

摘要

了解海洋生物如何适应当地环境对于预测种群如何应对全球气候变化至关重要。然而,人们对本地适应所涉及的基因组基础、环境因素和进化过程还不甚了解。在这里,我们以大西洋鲱鱼为模型生物来评估局部适应性。大西洋鲱鱼是一种数量丰富、洄游性强、分布广泛且拥有大量基因组资源的海洋鱼类。我们研究了加拿大大西洋和美国 15 个产卵群的基因组变异及其与广泛环境变量的相关性。然后,我们将研究结果与现有的大西洋东北部种群基因组数据进行了比较。我们证实,种群结构存在于基因组的一部分,其中包括可能具有重要功能的适应性基因变异。我们发现了分布在四条染色体上的 10 个高度分化的基因组区域。其中九个区域与季节性繁殖密切相关。其中一个区域与 12 号染色体上的已知反转相对应,是区分斯科舍大陆架生物地理过渡区南北种群的纬度模式的基础。基因组-环境关联表明,冬季海水温度与这一反转的纬度模式最为相关。与季节性繁殖有关的两个所谓 "分化岛 "的变化似乎与西北大西洋有关。大西洋西北部和东北部的种群共享其中四个分歧区域的变异,同时在另外四个区域的单倍型组成上表现出显著的多样性,其中包括 8 号染色体上一个未被描述的长约 7.7 Mb 的结构变异。我们的研究结果表明,产卵和早期发育的时间和地理位置可能在不同环境中受到与等位基因适应性有关的不同选择压力。我们的研究凸显了基因组结构、祖先单倍型和选择在维持种群规模大且可能基因流动频繁的物种的适应性分化中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adaptation to seasonal reproduction and environment-associated factors drive temporal and spatial differentiation in northwest Atlantic herring despite gene flow

Adaptation to seasonal reproduction and environment-associated factors drive temporal and spatial differentiation in northwest Atlantic herring despite gene flow

Understanding how marine organisms adapt to local environments is crucial for predicting how populations will respond to global climate change. The genomic basis, environmental factors and evolutionary processes involved in local adaptation are however not well understood. Here we use Atlantic herring, an abundant, migratory and widely distributed marine fish with substantial genomic resources, as a model organism to evaluate local adaptation. We examined genomic variation and its correlation with environmental variables across a broad environmental gradient, for 15 spawning aggregations in Atlantic Canada and the United States. We then compared our results with available genomic data of northeast Atlantic populations. We confirmed that population structure lies in a fraction of the genome including likely adaptive genetic variants of functional importance. We discovered 10 highly differentiated genomic regions distributed across four chromosomes. Nine regions show strong association with seasonal reproduction. One region, corresponding to a known inversion on chromosome 12, underlies a latitudinal pattern discriminating populations north and south of a biogeographic transition zone on the Scotian Shelf. Genome–environment associations indicate that winter seawater temperature best correlates with the latitudinal pattern of this inversion. The variation at two so-called ‘islands of divergence’ related to seasonal reproduction appear to be private to the northwest Atlantic. Populations in the northwest and northeast Atlantic share variation at four of these divergent regions, simultaneously displaying significant diversity in haplotype composition at another four regions, which includes an undescribed structural variant approximately 7.7 Mb long on chromosome 8. Our results suggest that the timing and geographic location of spawning and early development may be under diverse selective pressures related to allelic fitness across environments. Our study highlights the role of genomic architecture, ancestral haplotypes and selection in maintaining adaptive divergence in species with large population sizes and presumably high gene flow.

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来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
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