Comparative genomics provides insights into molecular adaptation to hypermetamorphosis and cantharidin metabolism in blister beetles (Coleoptera: Meloidae)

IF 3.5 1区 生物学 Q1 ZOOLOGY
Alessandra RICCIERI, Lucrezia SPAGONI, Ming LI, Paolo FRANCHINI, Marianna N. ROSSI, Emiliano FRATINI, Manuela CERVELLI, Marco A. BOLOGNA, Emiliano MANCINI
{"title":"Comparative genomics provides insights into molecular adaptation to hypermetamorphosis and cantharidin metabolism in blister beetles (Coleoptera: Meloidae)","authors":"Alessandra RICCIERI,&nbsp;Lucrezia SPAGONI,&nbsp;Ming LI,&nbsp;Paolo FRANCHINI,&nbsp;Marianna N. ROSSI,&nbsp;Emiliano FRATINI,&nbsp;Manuela CERVELLI,&nbsp;Marco A. BOLOGNA,&nbsp;Emiliano MANCINI","doi":"10.1111/1749-4877.12819","DOIUrl":null,"url":null,"abstract":"<p>Blister beetles (Coleoptera: Meloidae) are currently subdivided into three subfamilies: Eleticinae (a basal group), Nemognathinae, and Meloinae. These are all characterized by the endogenous production of the defensive terpene cantharidin (CA), whereas the two most derived subfamilies show a hypermetamorphic larval development. Here, we provide novel draft genome assemblies of five species sampled across the three blister beetle subfamilies (<i>Iselma pallidipennis</i>, <i>Stenodera caucasica</i>, <i>Zonitis immaculata</i>, <i>Lydus trimaculatus</i>, and <i>Mylabris variabilis</i>) and performed a comparative analysis with other available Meloidae genomes and the closely-related canthariphilous species (<i>Pyrochroa serraticornis</i>) to disclose adaptations at a molecular level. Our results highlighted the expansion and selection of genes potentially responsible for CA production and metabolism, as well as its mobilization and vesicular compartmentalization. Furthermore, we observed adaptive selection patterns and gain of genes devoted to epigenetic regulation, development, and morphogenesis, possibly related to hypermetamorphosis. We hypothesize that most genetic adaptations occurred to support both CA biosynthesis and hypermetamorphosis, two crucial aspects of Meloidae biology that likely contributed to their evolutionary success.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":null,"pages":null},"PeriodicalIF":3.5000,"publicationDate":"2024-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1749-4877.12819","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative zoology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1749-4877.12819","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Blister beetles (Coleoptera: Meloidae) are currently subdivided into three subfamilies: Eleticinae (a basal group), Nemognathinae, and Meloinae. These are all characterized by the endogenous production of the defensive terpene cantharidin (CA), whereas the two most derived subfamilies show a hypermetamorphic larval development. Here, we provide novel draft genome assemblies of five species sampled across the three blister beetle subfamilies (Iselma pallidipennis, Stenodera caucasica, Zonitis immaculata, Lydus trimaculatus, and Mylabris variabilis) and performed a comparative analysis with other available Meloidae genomes and the closely-related canthariphilous species (Pyrochroa serraticornis) to disclose adaptations at a molecular level. Our results highlighted the expansion and selection of genes potentially responsible for CA production and metabolism, as well as its mobilization and vesicular compartmentalization. Furthermore, we observed adaptive selection patterns and gain of genes devoted to epigenetic regulation, development, and morphogenesis, possibly related to hypermetamorphosis. We hypothesize that most genetic adaptations occurred to support both CA biosynthesis and hypermetamorphosis, two crucial aspects of Meloidae biology that likely contributed to their evolutionary success.

Abstract Image

Abstract Image

比较基因组学深入揭示了水泡甲虫(鞘翅目: Meloidae)对超变态的分子适应和胭脂虫素代谢。
水泡甲虫(鞘翅目: Meloidae)目前被细分为三个亚科:Eleticinae(基干亚科)、Nemognathinae 和 Meloinae。这三个亚科的特征都是内源产生防御性萜类化合物 cantharidin (CA),而两个最衍生的亚科则表现出幼虫发育的超变态性。在本文中,我们提供了三个水泡甲亚科中五个物种(Iselma pallidipennis、Stenodera caucasica、Zonitis immaculata、Lydus trimaculatus 和 Mylabris variabilis)的新基因组组装草案,并与其他可用的 Meloidae 基因组和密切相关的嗜萜物种(Pyrochroa serraticornis)进行了比较分析,以披露分子水平上的适应性。我们的研究结果突显了可能负责CA生产和代谢的基因的扩展和选择,以及CA的动员和囊泡分隔。此外,我们还观察到表观遗传调控、发育和形态发生基因的适应性选择模式和增殖,这可能与超变态有关。我们推测,大多数基因的适应都是为了支持CA的生物合成和超变态,这两个方面是Meloidae生物学的重要方面,很可能是它们进化成功的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.40
自引率
12.10%
发文量
81
审稿时长
>12 weeks
期刊介绍: The official journal of the International Society of Zoological Sciences focuses on zoology as an integrative discipline encompassing all aspects of animal life. It presents a broader perspective of many levels of zoological inquiry, both spatial and temporal, and encourages cooperation between zoology and other disciplines including, but not limited to, physics, computer science, social science, ethics, teaching, paleontology, molecular biology, physiology, behavior, ecology and the built environment. It also looks at the animal-human interaction through exploring animal-plant interactions, microbe/pathogen effects and global changes on the environment and human society. Integrative topics of greatest interest to INZ include: (1) Animals & climate change (2) Animals & pollution (3) Animals & infectious diseases (4) Animals & biological invasions (5) Animal-plant interactions (6) Zoogeography & paleontology (7) Neurons, genes & behavior (8) Molecular ecology & evolution (9) Physiological adaptations
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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