对鞘翅类翅膀的转录组学研究揭示了与甲虫鞘翅相关的新结构的进化

IF 1.8 3区 生物学 Q3 DEVELOPMENTAL BIOLOGY
David M. Linz, Yuichiro Hara, Kevin D. Deem, Shigehiro Kuraku, Shigeo Hayashi, Yoshinori Tomoyasu
{"title":"对鞘翅类翅膀的转录组学研究揭示了与甲虫鞘翅相关的新结构的进化","authors":"David M. Linz,&nbsp;Yuichiro Hara,&nbsp;Kevin D. Deem,&nbsp;Shigehiro Kuraku,&nbsp;Shigeo Hayashi,&nbsp;Yoshinori Tomoyasu","doi":"10.1002/jez.b.23188","DOIUrl":null,"url":null,"abstract":"<p>The acquisition of novel traits is central to organismal evolution, yet the molecular mechanisms underlying this process are elusive. The beetle forewings (elytra) are evolutionarily modified to serve as a protective shield, providing a unique opportunity to study these mechanisms. In the past, the orthologs of genes within the wing gene network from <i>Drosophila</i> studies served as the starting point when studying the evolution of elytra (candidate genes). Although effective, candidate gene lists are finite and only explore genes conserved across species. To go beyond candidate genes, we used RNA sequencing and explored the wing transcriptomes of two Coleopteran species, the red flour beetle (<i>Tribolium castaneum</i>) and the Japanese stag beetle (<i>Dorcus hopei</i>). Our analysis revealed sets of genes enriched in <i>Tribolium</i> elytra (57 genes) and genes unique to the hindwings, which possess more “typical” insect wing morphologies (29 genes). Over a third of the hindwing-enriched genes were “candidate genes” whose functions were previously analyzed in <i>Tribolium</i>, demonstrating the robustness of our sequencing. Although the overlap was limited, transcriptomic comparison between the beetle species found a common set of genes, including key wing genes, enriched in either elytra or hindwings. Our RNA interference analysis for elytron-enriched genes in <i>Tribolium</i> uncovered novel genes with roles in forming various aspects of morphology that are unique to elytra, such as pigmentation, hardening, sensory development, and vein formation. Our analyses deepen our understanding of how gene network evolution facilitated the emergence of the elytron, a unique structure critical to the evolutionary success of beetles.</p>","PeriodicalId":15682,"journal":{"name":"Journal of experimental zoology. Part B, Molecular and developmental evolution","volume":"340 2","pages":"197-213"},"PeriodicalIF":1.8000,"publicationDate":"2023-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/11/c8/JEZ-340-197.PMC10107685.pdf","citationCount":"1","resultStr":"{\"title\":\"Transcriptomic exploration of the Coleopteran wings reveals insight into the evolution of novel structures associated with the beetle elytron\",\"authors\":\"David M. Linz,&nbsp;Yuichiro Hara,&nbsp;Kevin D. Deem,&nbsp;Shigehiro Kuraku,&nbsp;Shigeo Hayashi,&nbsp;Yoshinori Tomoyasu\",\"doi\":\"10.1002/jez.b.23188\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The acquisition of novel traits is central to organismal evolution, yet the molecular mechanisms underlying this process are elusive. The beetle forewings (elytra) are evolutionarily modified to serve as a protective shield, providing a unique opportunity to study these mechanisms. In the past, the orthologs of genes within the wing gene network from <i>Drosophila</i> studies served as the starting point when studying the evolution of elytra (candidate genes). Although effective, candidate gene lists are finite and only explore genes conserved across species. To go beyond candidate genes, we used RNA sequencing and explored the wing transcriptomes of two Coleopteran species, the red flour beetle (<i>Tribolium castaneum</i>) and the Japanese stag beetle (<i>Dorcus hopei</i>). Our analysis revealed sets of genes enriched in <i>Tribolium</i> elytra (57 genes) and genes unique to the hindwings, which possess more “typical” insect wing morphologies (29 genes). Over a third of the hindwing-enriched genes were “candidate genes” whose functions were previously analyzed in <i>Tribolium</i>, demonstrating the robustness of our sequencing. Although the overlap was limited, transcriptomic comparison between the beetle species found a common set of genes, including key wing genes, enriched in either elytra or hindwings. Our RNA interference analysis for elytron-enriched genes in <i>Tribolium</i> uncovered novel genes with roles in forming various aspects of morphology that are unique to elytra, such as pigmentation, hardening, sensory development, and vein formation. Our analyses deepen our understanding of how gene network evolution facilitated the emergence of the elytron, a unique structure critical to the evolutionary success of beetles.</p>\",\"PeriodicalId\":15682,\"journal\":{\"name\":\"Journal of experimental zoology. Part B, Molecular and developmental evolution\",\"volume\":\"340 2\",\"pages\":\"197-213\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-01-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/11/c8/JEZ-340-197.PMC10107685.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of experimental zoology. Part B, Molecular and developmental evolution\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jez.b.23188\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental zoology. Part B, Molecular and developmental evolution","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jez.b.23188","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

新特征的获得是生物进化的核心,然而这一过程背后的分子机制是难以捉摸的。甲虫的前翅(鞘翅)在进化过程中被改造成一个保护盾,为研究这些机制提供了一个独特的机会。过去,在研究鞘翅(候选基因)进化时,以果蝇研究中翅膀基因网络内基因的同源物为出发点。虽然有效,但候选基因列表是有限的,并且只能探索跨物种保守的基因。为了超越候选基因,我们使用RNA测序并探索了两个鞘翅目物种,红粉甲虫(Tribolium castaneum)和日本鹿角甲虫(Dorcus hopei)的翅膀转录组。我们的分析揭示了Tribolium elytra中富含的基因组(57个基因)和后翅特有的基因组(29个基因),后者具有更“典型”的昆虫翅膀形态。超过三分之一的后翼富集基因是“候选基因”,其功能先前在Tribolium中分析过,证明了我们测序的稳健性。虽然重叠是有限的,但在甲虫物种之间的转录组学比较发现了一组共同的基因,包括关键的翅膀基因,在鞘翅或后翅中富集。我们对Tribolium中鞘翅富集基因的RNA干扰分析发现了新的基因,这些基因在形成鞘翅独特形态的各个方面发挥作用,如色素沉着、硬化、感觉发育和静脉形成。我们的分析加深了我们对基因网络进化如何促进鞘翅出现的理解,鞘翅是甲虫进化成功的一个独特结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic exploration of the Coleopteran wings reveals insight into the evolution of novel structures associated with the beetle elytron

Transcriptomic exploration of the Coleopteran wings reveals insight into the evolution of novel structures associated with the beetle elytron

The acquisition of novel traits is central to organismal evolution, yet the molecular mechanisms underlying this process are elusive. The beetle forewings (elytra) are evolutionarily modified to serve as a protective shield, providing a unique opportunity to study these mechanisms. In the past, the orthologs of genes within the wing gene network from Drosophila studies served as the starting point when studying the evolution of elytra (candidate genes). Although effective, candidate gene lists are finite and only explore genes conserved across species. To go beyond candidate genes, we used RNA sequencing and explored the wing transcriptomes of two Coleopteran species, the red flour beetle (Tribolium castaneum) and the Japanese stag beetle (Dorcus hopei). Our analysis revealed sets of genes enriched in Tribolium elytra (57 genes) and genes unique to the hindwings, which possess more “typical” insect wing morphologies (29 genes). Over a third of the hindwing-enriched genes were “candidate genes” whose functions were previously analyzed in Tribolium, demonstrating the robustness of our sequencing. Although the overlap was limited, transcriptomic comparison between the beetle species found a common set of genes, including key wing genes, enriched in either elytra or hindwings. Our RNA interference analysis for elytron-enriched genes in Tribolium uncovered novel genes with roles in forming various aspects of morphology that are unique to elytra, such as pigmentation, hardening, sensory development, and vein formation. Our analyses deepen our understanding of how gene network evolution facilitated the emergence of the elytron, a unique structure critical to the evolutionary success of beetles.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.80
自引率
9.10%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Developmental Evolution is a branch of evolutionary biology that integrates evidence and concepts from developmental biology, phylogenetics, comparative morphology, evolutionary genetics and increasingly also genomics, systems biology as well as synthetic biology to gain an understanding of the structure and evolution of organisms. The Journal of Experimental Zoology -B: Molecular and Developmental Evolution provides a forum where these fields are invited to bring together their insights to further a synthetic understanding of evolution from the molecular through the organismic level. Contributions from all these branches of science are welcome to JEZB. We particularly encourage submissions that apply the tools of genomics, as well as systems and synthetic biology to developmental evolution. At this time the impact of these emerging fields on developmental evolution has not been explored to its fullest extent and for this reason we are eager to foster the relationship of systems and synthetic biology with devo evo.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信