Genetic, developmental, and neural changes underlying the evolution of butterfly mate preference.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2025-03-11 eCollection Date: 2025-03-01 DOI:10.1371/journal.pbio.3002989
Nicholas W VanKuren, Nathan P Buerkle, Wei Lu, Erica L Westerman, Alexandria K Im, Darli Massardo, Laura Southcott, Stephanie E Palmer, Marcus R Kronforst
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Abstract

Many studies have linked genetic variation to behavior, but few connect to the intervening neural circuits that underlie the arc from sensation to action. Here, we used a combination of genome-wide association (GWA), developmental gene expression, and photoreceptor electrophysiology to investigate the architecture of mate choice behavior in Heliconius cydno butterflies, a clade where males identify preferred mates based on wing color patterns. We first found that the GWA variants most strongly associated with male mate choice were tightly linked to the gene controlling wing color in the K locus, consistent with previous mapping efforts. RNA-seq across developmental time points then showed that seven genes near the top GWA peaks were differentially expressed in the eyes, optic lobes, or central brain of white and yellow H. cydno males, many of which have known functions in the development and maintenance of synaptic connections. In the visual system of these butterflies, we identified a striking physiological difference between yellow and white males that could provide an evolutionarily labile circuit motif in the eye to rapidly switch behavioral preference. Using single-cell electrophysiology recordings, we found that some ultraviolet (UV)-sensitive photoreceptors receive inhibition from long-wavelength photoreceptors in the male eye. Surprisingly, the proportion of inhibited UV photoreceptors was strongly correlated with male wing color, suggesting a difference in the early stages of visual processing that could plausibly influence courtship decisions. We discuss potential links between candidate genes and this physiological signature, and suggest future avenues for experimental work. Taken together, our results support the idea that alterations to the evolutionarily labile peripheral nervous system, driven by genetic and gene expression differences, can significantly and rapidly alter essential behaviors.

许多研究将遗传变异与行为联系起来,但很少有研究将遗传变异与从感觉到行动的神经回路联系起来。在这里,我们结合使用了全基因组关联(GWA)、发育基因表达和光感受器电生理学,研究了Heliconius cydno蝴蝶择偶行为的结构。我们首先发现,与雄性择偶关系最密切的 GWA 变体与 K 基因座中控制翅膀颜色的基因紧密相连,这与之前的图谱研究结果一致。然后,跨发育时间点的 RNA 片段分析表明,GWA 最高峰附近的 7 个基因在白蝶和黄蝶雄性的眼睛、视叶或大脑中央有不同程度的表达,其中许多基因在突触连接的发育和维持方面具有已知的功能。在这些蝴蝶的视觉系统中,我们发现了黄雄蝶和白雄蝶之间的显著生理差异,这种差异可能在眼睛中提供了一种进化上易变的电路图案,以快速切换行为偏好。通过单细胞电生理学记录,我们发现雄蝶眼睛中一些对紫外线(UV)敏感的光感受器会受到来自长波长光感受器的抑制。令人惊讶的是,受抑制的紫外线光感受器的比例与雄性翅膀颜色密切相关,这表明视觉处理早期阶段的差异可能会影响求偶决定。我们讨论了候选基因与这种生理特征之间的潜在联系,并提出了未来实验工作的途径。总之,我们的研究结果支持这样一种观点,即在遗传和基因表达差异的驱动下,进化过程中易受影响的外周神经系统的改变可以显著而迅速地改变基本行为。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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