利用双目标归巢救援策略最大化大鼠基因驱动的根除潜力:经验数据的空间建模

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aysegul Birand, Luke Gierus, Thomas A. A. Prowse, Phillip Cassey, Paul Q. Thomas
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引用次数: 0

摘要

基因驱动是具有正向偏传的遗传因素,可能是抑制威胁全球生物多样性的哺乳动物害虫的有用工具。虽然基因驱动在小鼠身上取得了进展,但人们对其在侵入性大鼠控制方面的潜力知之甚少。最近的一份报告提供了大鼠生殖系基因转化的第一批数据,表明雌性可以实现适度的归巢率(高达67%)。在这里,我们利用我们的随机、空间明确、基于个体的建模框架,应用这些经验推导的值来研究各种基因驱动策略抑制20万只大鼠岛屿种群的潜力。嵌入单倍繁殖或生存基因的标准归巢驱动未能根除,但实现了永久的种群抑制。相比之下,在单致死基因中嵌入寻巢救援(HR)驱动的双靶点设计,也针对独立的生育或生存基因,显示出相当大的抑制潜力。值得注意的是,针对单倍足雌性生育基因的HR驱动即使在先前在大鼠中显示的相对较低的归巢率下也显示出强大的根除能力。有趣的是,归巢率对根除概率的影响相对较低,而单致死基因的切割效率至关重要。此外,只要后者与切割和随后的非连锁女性生育基因敲除相似,那么就可以在一定的归巢率范围内实现根除。总之,这些结果表明,适度的归巢率,比如在老鼠和其他物种中已经证明的,可以潜在地用于种群抑制,为基因驱动的发展提供新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maximising Eradication Potential of Rat Gene Drives Using a Two-Target Homing Rescue Strategy: Spatial Modelling of Empirical Data

Maximising Eradication Potential of Rat Gene Drives Using a Two-Target Homing Rescue Strategy: Spatial Modelling of Empirical Data

Gene drives are genetic elements with positively biased transmission and may be useful tools to suppress mammalian pests that threaten biodiversity worldwide. While gene drives are progressing in mice, less is known about their potential for invasive rat control. A recent report has provided the first data on germline gene conversion in rats, demonstrating that modest homing rates (up to 67%) can be achieved in females. Here, we apply these empirically derived values to investigate the potential of various gene drive strategies to suppress an island population of 200,000 rats, using our stochastic, spatially explicit, individual-based modelling framework. Standard homing drives embedded in haplosufficient fertility or viability genes failed to eradicate, but achieved permanent population suppression. In contrast, a two-target design with a homing rescue (HR) drive embedded in a haplolethal gene that also targets an independent fertility or viability gene demonstrated considerable suppression potential. Remarkably, an HR drive targeting a haplosufficient female fertility gene showed robust eradication even at the relatively low homing rates previously demonstrated in rats. Interestingly, homing rate had a relatively low influence on eradication probability while cutting efficiency at the haplolethal gene was critical. Further, as long as the latter was similar to the cutting and subsequent knockout of the unlinked female fertility gene, then eradication could be achieved across a range of homing rates. Together, these results suggest that modest homing rates, such as have been demonstrated in rats and other species, can potentially be leveraged for population suppression, offering new opportunities for gene drive development.

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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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