Optix 主要通过影响色素沉着来调节蝴蝶鳞片的纳米形态

IF 2.4 3区 环境科学与生态学 Q2 ECOLOGY
Tirtha Das Banerjee, Cédric Finet, Kwi Shan Seah, Antónia Monteiro
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引用次数: 0

摘要

先前的研究表明,Optix 可调节一些蝴蝶物种翅鳞的下层厚度和色素的产生类型。然而,Optix 在调节不同物种的色素生成以及调节鳞片形态的其他方面的作用仍有待研究。通过结合显微分光光度法、扫描电子显微镜和聚焦离子束技术对野生型和Optix Bicyclus anynana脆片进行研究,我们发现Optix能调节橙色色素(omochromes)的产生,抑制棕色色素(melanins)的产生,并调节橙色鳞片下表面和上表面的形态。我们的研究结果表明,Optix作为一个开关基因,在蝴蝶中具有激活omochromes和抑制黑色素合成的保守作用。通过将这些影响与其他只去除鳞片黑色素的基因突变进行比较,我们认为色素变化本身就会影响鳞片内几丁质的聚合方式,从而改变下层鳞片的厚度以及上表面的多种复杂结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optix regulates nanomorphology of butterfly scales primarily via its effects on pigmentation
Previous studies have shown that Optix regulates lower lamina thickness and the type of pigment that is produced in wing scales of a few butterfly species. However, the role of Optix in regulating pigment production across species, and in regulating additional aspects of scale morphology remains to be investigated. By combining microspectrophotometry, scanning electron microscopy, and focused ion beam technology on wild-type and Optix Bicyclus anynana crispants, we show that Optix regulates the production of orange pigments (ommochromes), represses the production of brown pigments (melanins), and regulates the morphology of the lower and upper surface of orange scales. Our findings suggest a conserved role of Optix as a switch gene that activates ommochrome and represses melanin synthesis across butterflies. By comparing these effects with other mutations, where only melanin is removed from scales, we propose that pigmentary changes, alone, affect the way that chitin polymerizes within a scale, changing lower lamina thickness as well as multiple intricate structures of the upper surface.
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来源期刊
Frontiers in Ecology and Evolution
Frontiers in Ecology and Evolution Environmental Science-Ecology
CiteScore
4.00
自引率
6.70%
发文量
1143
审稿时长
12 weeks
期刊介绍: Frontiers in Ecology and Evolution publishes rigorously peer-reviewed research across fundamental and applied sciences, to provide ecological and evolutionary insights into our natural and anthropogenic world, and how it should best be managed. Field Chief Editor Mark A. Elgar at the University of Melbourne is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Eminent biologist and theist Theodosius Dobzhansky’s astute observation that “Nothing in biology makes sense except in the light of evolution” has arguably even broader relevance now than when it was first penned in The American Biology Teacher in 1973. One could similarly argue that not much in evolution makes sense without recourse to ecological concepts: understanding diversity — from microbial adaptations to species assemblages — requires insights from both ecological and evolutionary disciplines. Nowadays, technological developments from other fields allow us to address unprecedented ecological and evolutionary questions of astonishing detail, impressive breadth and compelling inference. The specialty sections of Frontiers in Ecology and Evolution will publish, under a single platform, contemporary, rigorous research, reviews, opinions, and commentaries that cover the spectrum of ecological and evolutionary inquiry, both fundamental and applied. Articles are peer-reviewed according to the Frontiers review guidelines, which evaluate manuscripts on objective editorial criteria. Through this unique, Frontiers platform for open-access publishing and research networking, Frontiers in Ecology and Evolution aims to provide colleagues and the broader community with ecological and evolutionary insights into our natural and anthropogenic world, and how it might best be managed.
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