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首页> 外文期刊>Industrial and organizational psychology >Increased genetic marker density reveals high levels of admixture between red deer and introduced Japanese sika in Kintyre, Scotland
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Increased genetic marker density reveals high levels of admixture between red deer and introduced Japanese sika in Kintyre, Scotland

机译:增加的遗传标记密度揭示了红鹿和苏格兰克林特雷的日本锡卡在克林特雷介绍了高水平的混合物

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摘要

Hybridization is a natural process at species range boundaries, but increasing numbers of species are hybridizing due to direct or indirect human activities. In such cases of anthropogenic hybridization, subsequent introgression can threaten the survival of native species. To date, many such systems have been studied with too few genetic markers to assess the level of threat resulting from advanced backcrossing. Here, we use 44,999 single nucleotide polymorphisms (SNPs) and the ADMIXTURE program to study two areas of Scotland where a panel of 22 diagnostic microsatellites previously identified introgression between native red deer (Cervus elaphus) and introduced Japanese sika (Cervus nippon). In Kintyre, we reclassify 26% of deer from the pure species categories to the hybrid category whereas in the NW Highlands we only reclassify 2%. As expected, the reclassified individuals are mostly advanced backcrosses. We also investigate the ability of marker panels selected on different posterior allele frequency criteria to find hybrids assigned by the full marker set and show that in our data, ancestry informative markers (i.e. those that are highly differentiated between the species, but not fixed) are better than diagnostic markers (those markers that are fixed between the species) because they are more evenly distributed in the genome. Diagnostic loci are concentrated on the X chromosome to the detriment of autosomal coverage.
机译:杂交是物种范围边界的自然过程,但由于直接或间接人类活动,越来越多的物种杂交。在这种人为杂交的情况下,随后的渗入可能会威胁到原生物物种的存活。迄今为止,已经用太少的遗传标记进行了许多这样的系统,以评估高级回复导致的威胁水平。在这里,我们使用44,999个单核苷酸多态性(SNP)和混合物计划来研究苏格兰的两个区域,其中22个诊断微卫星先前鉴定了天然红鹿(颈椎)和引入日本SIKA(Cervus nippon)之间的血气。在克林特尔,我们将26%的鹿从纯物种类别中重新分类到混合类别,而在NW Highlands中,我们只会重新分类2%。正如预期的那样,重新分类的个体主要是先进的回复。我们还研究了在不同后等位基因频率标准上选择的标记面板的能力,以找到由完整标记集分配的混合动力,并显示在我们的数据中,祖先的信息标记(即物种之间具有高度区分的数据,但不固定)是优于诊断标记(在物种之间固定的那些标记),因为它们更均匀地分布在基因组中。诊断基因座浓缩在X染色体上,以损害常染色体覆盖率。

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