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The impact of mating systems and dispersal on fine-scale genetic structure at maternally, paternally and biparentally inherited markers

机译:交配系统和分散在母系,患者患者和两性继承标志物的微尺遗传结构上的影响

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For decades, studies have focused on how dispersal and mating systems influence genetic structure across populations or social groups. However, we still lack a thorough understanding of how these processes and their interaction shape spatial genetic patterns over a finer scale (tenshundreds of metres). Using uniparentally inherited markers may help answer these questions, yet their potential has not been fully explored. Here, we use individual-level simulations to investigate the effects of dispersal and mating system on fine-scale genetic structure at autosomal, mitochondrial and Y chromosome markers. Using genetic spatial autocorrelation analysis, we found that dispersal was the major driver of fine-scale genetic structure across maternally, paternally and biparentally inherited markers. However, when dispersal was restricted (mean distance=100m), variation in mating behaviour created strong differences in the comparative level of structure detected at maternally and paternally inherited markers. Promiscuity reduced spatial genetic structure at Y chromosome loci (relative to monogamy), whereas structure increased under polygyny. In contrast, mitochondrial and autosomal markers were robust to differences in the specific mating system, although genetic structure increased across all markers when reproductive success was skewed towards fewer individuals. Comparing males and females at Y chromosome vs. mitochondrial markers, respectively, revealed that some mating systems can generate similar patterns to those expected under sex-biased dispersal. This demonstrates the need for caution when inferring ecological and behavioural processes from genetic results. Comparing patterns between the sexes, across a range of marker types, may help us tease apart the processes shaping fine-scale genetic structure.
机译:几十年来,研究专注于分散和交配系统如何影响人口或社会群体的遗传结构。然而,我们仍然彻底了解这些过程如何以及它们在更精细的规模上(三通数米)的空间遗传模式。使用单一继承的标记可能有助于回答这些问题,但他们的潜力尚未完全探索。在这里,我们使用个性级模拟来研究分散和配合系统对常染色体,线粒体和Y染色体标记的细尺遗传结构的影响。使用遗传空间自相关分析,我们发现分散是潜水,患者和两性继承标志物的细尺遗传结构的主要驱动器。然而,当分散的限制(平均距离= 100m)时,配合行为的变化在潜水和宠物遗传标记处检测到的比较结构中产生强烈差异。滥交降低了Y染色体基因座(相对于单羊毛)的空间遗传结构,而结构在Polygyny下增加。相反,线粒体和常染色体标记对于特定配合系统的差异是强大的,尽管当生殖成功偏向更少的个体时,遗传结构在所有标记上增加了遗传结构。在Y染色体与线粒体标记物中比较男性和雌性,揭示了一些配合系统可以在性偏见的分散下的预期产生类似的模式。这证明了在从遗传结果推断生态和行为过程时谨慎的需要。比较性别之间的模式,在一系列标记类型中,可以帮助我们挑逗整形细尺遗传结构的过程。

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