两个报春花杂交带的基因组分化和基因渗入模式。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Huiqin Yi, Lihua Yang, Ming Kang
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引用次数: 0

摘要

杂交带一直被认为是了解物种形成机制的自然实验室。多个或复制的杂交区尤其具有信息性,因为它们允许评估不同环境背景和人口历史中基因组分化和渗入的一致性,从而提高我们对在更大范围内驱动或阻碍物种形成的因素的理解。本文利用全基因组重测序数据,比较了两个报春花杂交带的基因组分化和基因渗入模式。我们发现,这两个杂交区域的基因组分化在很大程度上是由中性过程形成的,只有少数基因组区域显示出平衡或谱系特异性选择的特征。基因组突变分析发现,在两个杂交区,许多snp显示出比全基因组预期更陡峭的曲线和偏中心,这与生殖障碍的存在一致。在基因流动受限区域内,我们鉴定出21个基因在两个杂交区之间共享。基因功能的注释揭示了几个基因参与生殖过程。此外,许多区域特异性异常位点与花粉和花朵发育相关的基因相关,表明这些障碍可能有助于局部生态条件下的生殖隔离。总的来说,这些发现表明,虽然某些生殖障碍在独立杂交区保持一致,但其他障碍可能取决于当地的环境背景。我们的研究结果表明,Primulina的一般机制和区域特异性机制都有助于生殖隔离,提供了经验证据,表明一些基因组障碍在独立杂交区域重复出现,而另一些则通过局部适应产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patterns of Genomic Divergence and Introgression in Two Primulina Hybrid Zones.

Hybrid zones have long been promoted as natural laboratories for understanding the mechanisms of speciation. Multiple or replicated hybrid zones are particularly informative, as they allow for assessing the consistency of genomic divergence and introgression across different environmental contexts and demographic histories, thereby improving our understanding of the factors that drive or hinder speciation on a broader scale. Here, using whole-genome resequencing data, we compare the patterns of genomic divergence and introgression in two Primulina hybrid zones. We found that genomic divergence in both hybrid zones is largely shaped by neutral processes, with only a few genomic regions showing signatures of balancing or lineage-specific selection. Genomic cline analyses identified numerous SNPs that showed significantly steeper clines and biased centres than the genome-wide expectation in both hybrid zones, consistent with the existence of reproductive barriers. Within regions of restricted gene flow, we identified 21 genes shared between the two hybrid zones. Annotation of gene function revealed that several genes are involved in reproductive processes. In addition, many zone-specific outlier loci were linked to genes associated with pollen and flower development, suggesting that these barriers may contribute to reproductive isolation under localised ecological conditions. Overall, these findings suggest that while certain reproductive barriers remain consistent across independent hybrid zones, others may be contingent on local environmental contexts. Our results demonstrate that both general and zone-specific mechanisms contribute to reproductive isolation in Primulina, providing empirical evidence that some genomic barriers recur across independent hybrid zones while others arise through localised adaptation.

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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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