Reproductive isolation arises during laboratory adaptation to a novel hot environment.

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Sheng-Kai Hsu, Wei-Yun Lai, Johannes Novak, Felix Lehner, Ana Marija Jakšić, Elisabetta Versace, Christian Schlötterer
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Abstract

Background: Reproductive isolation can result from adaptive processes (e.g., ecological speciation and mutation-order speciation) or stochastic processes such as "system drift" model. Ecological speciation predicts barriers to gene flow between populations from different environments, but not among replicate populations from the same environment. In contrast, reproductive isolation among populations independently adapted to the same/similar environment can arise from both mutation-order speciation or system drift.

Results: In experimentally evolved populations adapting to a hot environment for over 100 generations, we find evidence for pre- and postmating reproductive isolation. On one hand, an altered lipid metabolism and cuticular hydrocarbon composition pointed to possible premating barriers between the ancestral and replicate evolved populations. On the other hand, the pronounced gene expression differences in male reproductive genes may underlie the postmating isolation among replicate evolved populations adapting to the same environment with the same standing genetic variation.

Conclusion: Our study confirms that replicated evolution experiments provide valuable insights into the mechanisms of speciation. The rapid emergence of the premating reproductive isolation during temperature adaptation showcases incipient ecological speciation. The potential evidence of postmating reproductive isolation among replicates gave rise to two hypotheses: (1) mutation-order speciation through a common selection on early fecundity leading to an inherent inter-locus sexual conflict; (2) system drift with genetic drift along the neutral ridges.

在实验室适应新的高温环境的过程中出现了生殖隔离。
背景:生殖隔离可由适应过程(如生态分化和变异阶梯分化)或随机过程(如 "系统漂移 "模型)引起。生态种群分化预示着来自不同环境的种群之间存在基因流动障碍,但来自同一环境的复制种群之间却不存在基因流动障碍。与此相反,独立适应相同/相似环境的种群之间的生殖隔离可能来自突变阶梯式的物种分化或系统漂移:结果:在适应炎热环境超过 100 代的实验进化种群中,我们发现了交配前和交配后生殖隔离的证据。一方面,脂质代谢和角质烃组成的改变表明,祖先种群和复制进化种群之间可能存在交配前障碍。另一方面,雄性生殖基因在基因表达上的明显差异,可能是适应相同环境、具有相同遗传变异的复制进化种群在交配后出现隔离的原因:我们的研究证实,复制进化实验为物种演化机制提供了宝贵的见解。在温度适应过程中迅速出现的交配前生殖隔离显示了生态物种分化的萌芽。复制样本间交配后生殖隔离的潜在证据提出了两个假设:(1)通过对早期繁殖力的共同选择导致病灶间固有的性冲突,从而产生突变阶梯式物种分化;(2)系统漂移与沿中性脊的遗传漂移。
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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