群体抑制的合成基因驱动的自然选择倾向于一种中等强度的驱动。

IF 2.7 2区 环境科学与生态学 Q2 ECOLOGY
American Naturalist Pub Date : 2025-09-01 Epub Date: 2025-07-11 DOI:10.1086/736727
P J Beaghton, Austin Burt
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引用次数: 0

摘要

摘要合成基因驱动作为抑制害虫种群的工具正在被研究,了解自然选择如何作用于可能由新生突变产生或有意释放的变异驱动是很重要的。在这项研究中,我们扩展了以前的空间隐式随机模型,以研究斑块环境中当种群大小动态响应驱动因子的扩散时,合成驱动Y染色体的进化动力学,并推导出驱动强度存在进化稳定策略(ESS)的条件。在广泛的条件下,一种中等驱动强度作为ESS出现,能够胜过较强和较弱的变体。此外,我们还展示了故意释放跨越ESS的两个驾驶员如何有助于稳定种群动态。最后,近交抑制具有扩大不存在中间ESS的条件范围的作用,在种群被淘汰之前,选择越来越强的驱动。这些结果为基因驱动系统的预期进化轨迹提供了见解,对害虫和病媒控制中基因驱动的设计和释放具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Selection of Synthetic Gene Drives for Population Suppression Can Favor an Intermediate Strength of Drive.

AbstractSynthetic gene drives are being investigated as tools to suppress pest populations, and it is important to understand how natural selection will act on variant drivers that may either arise by de novo mutation or be intentionally released. In this study, we extend previous spatially implicit stochastic models to examine the evolutionary dynamics of synthetic driving Y chromosomes in patchy environments when population size is responding dynamically to the spread of the driver and derive conditions for the existence of an evolutionarily stable strategy (ESS) for drive strength. Under broad conditions, an intermediate drive strength emerges as the ESS, capable of outcompeting both stronger and weaker variants. Additionally, we show how the intentional release of two drivers straddling the ESS can help stabilize population dynamics. Finally, inbreeding depression has the effect of expanding the range of conditions under which no intermediate ESS exists, with ever stronger drive being selected until the population is eliminated. These results provide insights into the expected evolutionary trajectories of gene drive systems, with important implications for the design and release of gene drives for pest and vector control.

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来源期刊
American Naturalist
American Naturalist 环境科学-进化生物学
CiteScore
5.40
自引率
3.40%
发文量
194
审稿时长
3 months
期刊介绍: Since its inception in 1867, The American Naturalist has maintained its position as one of the world''s premier peer-reviewed publications in ecology, evolution, and behavior research. Its goals are to publish articles that are of broad interest to the readership, pose new and significant problems, introduce novel subjects, develop conceptual unification, and change the way people think. AmNat emphasizes sophisticated methodologies and innovative theoretical syntheses—all in an effort to advance the knowledge of organic evolution and other broad biological principles.
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