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被自己的火药炸飞:果蝇亲缘关系中的性别比例减数驱动如何创造限制其传播的抗性等位基因。

Hoisted with his own petard: How sex-ratio meiotic drive in Drosophila affinis creates resistance alleles that limit its spread.

机构信息

Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, USA.

出版信息

J Evol Biol. 2022 Dec;35(12):1765-1776. doi: 10.1111/jeb.14077. Epub 2022 Aug 23.

Abstract

Meiotic drivers are selfish genetic elements that tinker with gametogenesis to bias their own transmission into the next generation of offspring. Such tinkering can have significant consequences on gametogenesis and end up hampering the spread of the driver. In Drosophila affinis, sex-ratio meiotic drive is caused by an X-linked complex that, when in males with a susceptible Y chromosome, results in broods that are typically more than 95% female. Interestingly, D. affinis males lacking a Y chromosome (XO) are fertile and males with the meiotic drive X and no Y produce only sons-effectively reversing the sex-ratio effect. Here, we show that meiotic drive dramatically increases the rate of nondisjunction of the Y chromosome (at least 750X), meaning that the driver is creating resistant alleles through the process of driving. We then model how the O might influence the spread, dynamics and equilibrium of the sex-ratio X chromosome. We find that the O can prevent the spread or reduce the equilibrium frequency of the sex-ratio X chromosome, and it can even lead to oscillations in frequency. Finally, with reasonable parameters, the O is unlikely to lead to the loss of the Y chromosome, but we discuss how it might lead to sex-chromosome turnover indirectly.

摘要

减数分裂驱动因子是自私的遗传因子,它们会干预配子发生过程,以使自身在后代中得到更多的传递。这种干预可能会对配子发生产生重大影响,并最终阻碍驱动因子的传播。在果蝇 affinis 中,性比率减数分裂驱动是由一个 X 连锁复合物引起的,当它存在于易感性 Y 染色体的雄性中时,会导致后代中通常超过 95%是雌性。有趣的是,缺乏 Y 染色体的 D. affinis 雄性(XO)是可育的,而带有减数分裂驱动 X 和没有 Y 的雄性只产生雄性——有效地反转了性比率效应。在这里,我们表明减数分裂驱动显著增加了 Y 染色体的非分离率(至少 750X),这意味着驱动因子通过驱动过程创造了抗性等位基因。然后,我们模拟了 O 如何影响性比率 X 染色体的传播、动态和平衡。我们发现,O 可以阻止性比率 X 染色体的传播或降低其平衡频率,甚至可以导致频率的振荡。最后,在合理的参数下,O 不太可能导致 Y 染色体的丢失,但我们讨论了它如何间接地导致性染色体的转换。

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