由于动物类群的杂合性增加,基因拯救往往会带来更高的适应性

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Julia G. Clarke, Adam C. Smith, Catherine I. Cullingham
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引用次数: 0

摘要

生物多样性的丧失已达到临界水平,部分原因是人为造成的生境丧失和退化。这些景观变化具有破坏性,因为它们会将物种分布分割成孤立的小种群,导致基因流动受限、种群数量减少和适应潜力降低。基因拯救,即通过转移个体来增加遗传多样性并最终提高适应性,在破碎化种群中取得了可喜的成果,但由于缺乏长期数据和监测,仍未得到充分利用。为了更好地了解基因拯救及其短期内的潜在风险和益处,我们对已发表的基因拯救尝试进行了回顾和分析,以确定基因迁移后遗传多样性是否会增加,以及这种变化是否与适应性的提高有关。我们的综述确定了 19 项研究,这些研究提供了易位前后的遗传和适应性数据;其中大部分是关于哺乳动物的研究,包括实验性、自然性和保护性易位。利用贝叶斯元分析方法,我们发现平均而言,迁移后种群的遗传多样性和适应性都有所提高,但这一趋势也有例外。总体而言,遗传多样性对种群的适应性有积极的预测作用,在某些情况下,这种关系会在拯救后延续三代。这些数据表明,一次迁移就能带来持久的适应性益处,并支持将迁移作为另一种促进保护成功的工具。鉴于具有长期数据的研究数量有限,我们认为有必要对迁移后的种群进行遗传监测,以了解遗传拯救是否也能限制适应潜力的长期丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genetic rescue often leads to higher fitness as a result of increased heterozygosity across animal taxa

Genetic rescue often leads to higher fitness as a result of increased heterozygosity across animal taxa

Biodiversity loss has reached critical levels partly due to anthropogenic habitat loss and degradation. These landscape changes are damaging as they can fragment species distributions into small, isolated populations, resulting in limited gene flow, population declines and reduced adaptive potential. Genetic rescue, the translocation of individuals to increase genetic diversity and ultimately fitness, has produced promising results for fragmented populations but remains underutilized due to a lack of long-term data and monitoring. To promote a better understanding of genetic rescue and its potential risks and benefits over the short-term, we reviewed and analysed published genetic rescue attempts to identify whether genetic diversity increases following translocation, and if this change is associated with increased fitness. Our review identified 19 studies that provided genetic and fitness data from before and after the translocation; the majority of these were on mammals, and included experimental, natural and conservation-motivated translocations. Using a Bayesian meta-analytical approach, we found that on average, genetic diversity and fitness increased in populations post translocations, although there were some exceptions to this trend. Overall, genetic diversity was a positive predictor of population fitness, and in some cases this relationship extended three generations post-rescue. These data suggest a single translocation can have lasting fitness benefits, and support translocation as another tool to facilitate conservation success. Given the limited number of studies with long-term data, we echo the need for genetic monitoring of populations post-translocation to understand whether genetic rescue can also limit the loss of adaptive potential in the long-term.

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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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