Black John G, Cooper Steven J B, Schmidt Thomas L, Weeks Andrew R
School of Biosciences The University of Melbourne Melbourne Victoria Australia.
School of Biological Sciences and the Environment Institute The University of Adelaide Adelaide South Australia Australia.
Evol Appl. 2024 Dec 5;17(12):e70050. doi: 10.1111/eva.70050. eCollection 2024 Dec.
Genetic mixing aims to increase the genetic diversity of small or isolated populations, by mitigating genetic drift and inbreeding depression, either by maximally increasing genetic diversity, or minimising the prevalence of recessive, deleterious alleles. However, few studies investigate this beyond a single generation of mixing. Here, we model genetic mixing using captive, low-diversity recipient population of the threatened Southern brown bandicoot () over 50 generations and compare wild populations across south-eastern Australia as candidate source populations. We first assess genetic differentiation between 12 populations, including the first genomic assessment of three mainland Australian and three Tasmanian populations. We assess genetic diversity in the 12 populations using an individualised autosomal heterozygosity pipeline, using these results to identify a candidate recipient population for genetic mixing simulations. We found that populations fell into four major groups of genetic similarity: Adelaide Hills, western Victoria, eastern Victoria, and Tasmania, but populations within these groups were also distinct, and additional substructure was observed in some populations. Our autosomal heterozygosity pipeline indicated significant variability in mean heterozygosity between populations, identifying one extremely genetically degraded population on Inner Sister Island, Tasmania. Genetic mixing simulations of a low heterozygosity captive population in Victoria suggested the greatest increase in heterozygosity would be reached by using highly differentiated populations as mixing sources. However, when removing populations that may represent taxonomically discrete lineages, neither metrics of differentiation nor heterozygosity was strongly correlated with modelled heterozygosity increase, indicating the value of simulation-based approaches when selecting source populations for population mixing.
基因混合旨在通过减轻遗传漂变和近亲繁殖衰退来增加小型或孤立种群的遗传多样性,方法是最大限度地增加遗传多样性,或尽量减少隐性有害等位基因的流行。然而,很少有研究在一代以上的混合过程中对此进行调查。在这里,我们对受威胁的南褐袋狸()的圈养、低多样性受体种群进行了50代的基因混合建模,并将澳大利亚东南部的野生种群作为候选来源种群进行比较。我们首先评估了12个种群之间的遗传分化,包括对三个澳大利亚大陆种群和三个塔斯马尼亚种群的首次基因组评估。我们使用个性化的常染色体杂合度管道评估了这12个种群的遗传多样性,并利用这些结果确定了一个用于基因混合模拟的候选受体种群。我们发现,种群分为四个主要的遗传相似组:阿德莱德山、维多利亚西部、维多利亚东部和塔斯马尼亚,但这些组内的种群也各不相同,并且在一些种群中观察到了额外的亚结构。我们的常染色体杂合度管道表明,种群之间的平均杂合度存在显著差异,确定了塔斯马尼亚内姐妹岛上一个遗传极度退化的种群。对维多利亚州一个低杂合度圈养种群的基因混合模拟表明,使用高度分化的种群作为混合源将使杂合度增加最多。然而,当去除可能代表分类学上离散谱系的种群时,分化指标和杂合度都与模拟的杂合度增加没有强烈的相关性,这表明在为种群混合选择源种群时,基于模拟的方法具有价值。