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Genomic analyses identify multiple Asian origins and deeply diverged mitochondrial clades in inbred brown rats (Rattus norvegicus)

机译:基因组分析确定了近交棕色大鼠(Rattus norvegicus)的多个亚洲起源和线粒体进化分支

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摘要

Over 500 strains of inbred brown rats (Rattus norvegicus) have been developed for use as a biomedical model organism. Most of these inbred lines were derived from the colony established at the Wistar Institute in 1906 or its descendants following worldwide distribution to research and breeding centers. The geographic source of the animals that founded the Wistar colony has been lost to history; thus, we compared 25 inbred rat strains to 326 wild rats from a global diversity dataset at 32 k SNPs, and 47 mitochondrial genomes to identify the source populations. We analyzed nuclear genomic data using principal component analyses and co‐ancestry heat maps, and mitogenomes using phylogenetic trees and networks. In the nuclear genome, inbred rats clustered together indicating a single geographic origin for the strains studied and showed admixed ancestral variation with wild rats in eastern Asia and western North America. The Sprague Dawley derived, Wistar derived, and Brown Norway strains each had mitogenomes from different clades which diverged between 13 and 139 kya. Thus, we posit that rats originally collected for captive breeding had high mitochondrial diversity that became fixed through genetic drift and/or artificial selection. Our results show that these important medical models share common genomic ancestry from a few source populations, and opportunities exist to create new strains with diverse genomic backgrounds to provide novel insight into the genomic basis of disease phenotypes.
机译:已经开发了超过500个近交棕色大鼠(Rattus norvegicus)用作生物医学模型生物。这些近交系大部分来自于1906年在Wistar研究所建立的殖民地或其后代,在全球范围内分布到研究和繁育中心。建立Wistar殖民地的动物的地理来源已被遗忘;因此,我们从32 k SNPs和47个线粒体基因组的全球多样性数据集中,将25个自交系大鼠菌株与326只野生大鼠进行了比较,以鉴定来源种群。我们使用主成分分析和祖先热图分析了核基因组数据,并使用系统树和网络分析了有丝分裂基因组。在核基因组中,近交大鼠聚集在一起,表明所研究的菌株具有单一地理起源,并且与东亚和北美西部的野生大鼠显示出原始的祖先变异。 Sprague Dawley衍生株,Wistar衍生株和Brown Norway株分别具有来自不同进化枝的有丝分裂基因组,这些进化枝在13至139 kya之间分化。因此,我们假设最初为圈养繁殖而收集的大鼠具有较高的线粒体多样性,这种线粒体多样性通过遗传漂移和/或人工选择而变得固定。我们的结果表明,这些重要的医学模型从少数几个来源群体中共享共同的基因组血统,并且存在创造具有不同基因组背景的新菌株的机会,从而为疾病表型的基因组基础提供新颖的见解。

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