Conservation Mitonuclear Replacement: Facilitated mitochondrial adaptation for a changing world

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Erik N. K. Iverson
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Abstract

Most species will not be able to migrate fast enough to cope with climate change, nor evolve quickly enough with current levels of genetic variation. Exacerbating the problem are anthropogenic influences on adaptive potential, including the prevention of gene flow through habitat fragmentation and the erosion of genetic diversity in small, bottlenecked populations. Facilitated adaptation, or assisted evolution, offers a way to augment adaptive genetic variation via artificial selection, induced hybridization, or genetic engineering. One key source of genetic variation, particularly for climatic adaptation, are the core metabolic genes encoded by the mitochondrial genome. These genes influence environmental tolerance to heat, drought, and hypoxia, but must interact intimately and co-evolve with a suite of important nuclear genes. These coadapted mitonuclear genes form some of the important reproductive barriers between species. Mitochondrial genomes can and do introgress between species in an adaptive manner, and they may co-introgress with nuclear genes important for maintaining mitonuclear compatibility. Managers should consider the relevance of mitonuclear genetic variability in conservation decision-making, including as a tool for facilitating adaptation. I propose a novel technique dubbed Conservation Mitonuclear Replacement (CmNR), which entails replacing the core metabolic machinery of a threatened species—the mitochondrial genome and key nuclear loci—with those from a closely related species or a divergent population, which may be better-adapted to climatic changes or carry a lower genetic load. The most feasible route to CmNR is to combine CRISPR-based nuclear genetic editing with mitochondrial replacement and assisted reproductive technologies. This method preserves much of an organism's phenotype and could allow populations to persist in the wild when no other suitable conservation options exist. The technique could be particularly important on mountaintops, where rising temperatures threaten an alarming number of species with almost certain extinction in the next century.

Abstract Image

保护性线粒体核替代:促进线粒体适应不断变化的世界
大多数物种无法以足够快的速度迁徙以应对气候变化,也无法以目前的遗传变异水平迅速进化。人类活动对适应潜力的影响加剧了这一问题,包括通过生境破碎化阻止基因流动,以及侵蚀小型瓶颈种群的遗传多样性。促进适应或辅助进化提供了一种通过人工选择、诱导杂交或基因工程来增强适应性遗传变异的方法。线粒体基因组编码的核心代谢基因是遗传变异,尤其是气候适应性遗传变异的一个关键来源。这些基因影响着对高温、干旱和缺氧的环境耐受性,但必须与一系列重要的核基因密切互动和共同进化。这些共同适应的有丝分裂核基因构成了物种间一些重要的生殖屏障。线粒体基因组可以而且确实以适应性的方式在物种之间进行导入,它们可能与对维持有丝分裂核兼容性非常重要的核基因共同导入。管理者应考虑有丝分裂核基因变异在保护决策中的相关性,包括将其作为促进适应的工具。我提出了一种名为 "保护性线粒体核替换(CmNR)"的新技术,即用近缘物种或分化种群的线粒体基因组和关键核基因位点替换受威胁物种的核心代谢机制。实现 CmNR 的最可行途径是将基于 CRISPR 的核基因编辑与线粒体置换和辅助生殖技术相结合。这种方法可以保留生物的大部分表型,在没有其他合适的保护方案时,可以让种群在野外存活下来。这项技术在山顶上可能尤为重要,因为气温升高会威胁到数量惊人的物种,它们几乎肯定会在下个世纪灭绝。
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来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
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