Selection on genes associated with the evolution of divergent life histories: Gamete recognition or something else?

IF 2.6 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY Evolution & Development Pub Date : 2021-09-21 DOI:10.1111/ede.12392
Vanessa I. Guerra, Gwilym Haynes, Maria Byrne, Michael W. Hart
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引用次数: 1

Abstract

Gamete compatibility, and fertilization success, is mediated by gamete-recognition genes (GRGs) that are expected to show genetic evidence of a response to sexual selection associated with mating system traits. Changes in the strength of sexual selection can arise from the resolution of sperm competition among males, sexual conflicts of interest between males and females, or other mechanisms of sexual selection. To assess these expectations, we compared patterns of episodic diversifying selection among genes expressed in the gonads of Cryptasterina pentagona and C. hystera, which recently speciated and have evolved different mating systems (gonochoric or hermaphroditic), modes of fertilization (outcrossing or selfing), and dispersal (planktonic larvae or internal brooding). Cryptasterina spp. inhabit the upper intertidal of the coast of Queensland and coral islands of the Great Barrier Reef. We found some evidence for positive selection on a GRG in the outcrossing C. pentagona, and we found evidence of loss of gene function in a GRG of the self-fertilizing C. hystera. The modification or loss of gene functionality may be evidence of relaxed selection on some aspects of gamete interaction in C. hystera. In addition to these genes involved in gamete interactions, we also found genes under selection linked to abiotic stress, chromosomal regulation, polyspermy, and egg-laying. We interpret those results as possible evidence that Cryptasterina spp. with different mating systems may have been adapting in divergent ways to oxidative stress or other factors associated with reproduction in the physiologically challenging environment of the high intertidal.

Research Highlights

Recent speciation between two sea stars was unlikely the result of selection on gamete-recognition genes annotated in this study. Instead, our results point to selection on genes linked to the intertidal environment and reproduction.

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与不同生命史进化相关的基因选择:配子识别还是别的什么?
配子兼容性和受精成功是由配子识别基因(GRGs)介导的,该基因有望显示与交配系统特征相关的性选择反应的遗传证据。性选择强度的变化可能源于雄性之间精子竞争的解决,雄性和雌性之间的性利益冲突,或其他性选择机制。为了评估这些期望,我们比较了最近形成并进化出不同交配系统(雌雄同体或雌雄同体)、受精模式(异交或自交)和扩散(浮游幼虫或内部孵化)的五角形隐蝽和子宫隐蝽性腺中表达的基因的偶发多样化选择模式。隐翅虫栖息在昆士兰海岸的潮间带上部和大堡礁的珊瑚岛上。我们在异交五角草中发现了GRG阳性选择的证据,而在自受精的子宫草中发现了GRG基因功能缺失的证据。基因功能的改变或丧失可能是在配子相互作用的某些方面放松选择的证据。除了这些参与配子相互作用的基因外,我们还发现了与非生物胁迫、染色体调节、多精和产卵有关的选择基因。我们将这些结果解释为可能的证据,表明在高潮间带的生理挑战环境中,具有不同交配系统的隐盘虫可能以不同的方式适应氧化应激或其他与繁殖相关的因素。两颗海星之间最近的物种形成不太可能是本研究中注释的配子识别基因选择的结果。相反,我们的结果指向了与潮间带环境和繁殖有关的基因选择。
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来源期刊
Evolution & Development
Evolution & Development 生物-发育生物学
CiteScore
6.30
自引率
3.40%
发文量
26
审稿时长
>12 weeks
期刊介绍: Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.
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