Molecular signatures of diapause in the Asian longhorned beetle: Gene expression

IF 2.2 Q1 ENTOMOLOGY
Alex S. Torson , Susan Bowman , Daniel Doucet , Amanda D. Roe , Brent J. Sinclair
{"title":"Molecular signatures of diapause in the Asian longhorned beetle: Gene expression","authors":"Alex S. Torson ,&nbsp;Susan Bowman ,&nbsp;Daniel Doucet ,&nbsp;Amanda D. Roe ,&nbsp;Brent J. Sinclair","doi":"10.1016/j.cris.2023.100054","DOIUrl":null,"url":null,"abstract":"<div><p>Most previous studies on gene expression during insect diapause do not address among-tissue variation in physiological processes. We measured transcriptomic changes during larval diapause in the Asian longhorned beetle, <em>Anoplophora glabripennis</em> (Coleoptera: Cerambycidae)<em>.</em> We conducted RNA-seq on fat body, the supraesophageal ganglion, midgut, hindgut, and Malpighian tubules during pre-diapause, diapause maintenance, post-diapause quiescence, and post-diapause development. We observed a small, but consistent, proportion of genes within each gene expression profile that were shared among tissues, lending support for a core set of diapause-associated genes whose expression is tissue-independent. We evaluated the overarching hypotheses that diapause would be associated with cell cycle arrest, developmental arrest, and increased stress tolerance and found evidence of repressed TOR and insulin signaling, reduced cell cycle activity and increased capacity of stress response via heat shock protein expression and remodeling of the cytoskeleton. However, these processes varied among tissues, with the brain and fat body appearing to maintain higher levels of cellular activity during diapause than the midgut or Malpighian tubules. We also observed temperature-dependent changes in gene expression during diapause maintenance, particularly in genes related to the heat shock response and MAPK, insulin, and TOR signaling pathways. Additionally, we provide evidence for epigenetic reorganization during the diapause/post-diapause quiescence transition and expression of genes involved in post-translational modification, highlighting the need for investigations of the protein activity of these candidate genes and processes. We conclude that diapause development is coordinated via diverse tissue-specific gene expression profiles and that canonical diapause phenotypes vary among tissues.</p></div>","PeriodicalId":34629,"journal":{"name":"Current Research in Insect Science","volume":"3 ","pages":"Article 100054"},"PeriodicalIF":2.2000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074507/pdf/main.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Insect Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666515823000033","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Most previous studies on gene expression during insect diapause do not address among-tissue variation in physiological processes. We measured transcriptomic changes during larval diapause in the Asian longhorned beetle, Anoplophora glabripennis (Coleoptera: Cerambycidae). We conducted RNA-seq on fat body, the supraesophageal ganglion, midgut, hindgut, and Malpighian tubules during pre-diapause, diapause maintenance, post-diapause quiescence, and post-diapause development. We observed a small, but consistent, proportion of genes within each gene expression profile that were shared among tissues, lending support for a core set of diapause-associated genes whose expression is tissue-independent. We evaluated the overarching hypotheses that diapause would be associated with cell cycle arrest, developmental arrest, and increased stress tolerance and found evidence of repressed TOR and insulin signaling, reduced cell cycle activity and increased capacity of stress response via heat shock protein expression and remodeling of the cytoskeleton. However, these processes varied among tissues, with the brain and fat body appearing to maintain higher levels of cellular activity during diapause than the midgut or Malpighian tubules. We also observed temperature-dependent changes in gene expression during diapause maintenance, particularly in genes related to the heat shock response and MAPK, insulin, and TOR signaling pathways. Additionally, we provide evidence for epigenetic reorganization during the diapause/post-diapause quiescence transition and expression of genes involved in post-translational modification, highlighting the need for investigations of the protein activity of these candidate genes and processes. We conclude that diapause development is coordinated via diverse tissue-specific gene expression profiles and that canonical diapause phenotypes vary among tissues.

亚洲长角甲虫滞育的分子特征:基因表达
以前关于昆虫滞育过程中基因表达的大多数研究都没有涉及生理过程中组织间的变化。我们测量了亚洲长角甲虫光肩星天牛幼虫滞育期间的转录组变化。在滞育前、滞育维持、滞育后静止和滞育后发育过程中,我们对脂肪体、食管上神经节、中肠、后肠和马尔皮氏管进行了RNA-seq。我们观察到,在每个基因表达谱中,组织之间共享的基因比例很小,但一致,这为滞育相关基因的核心集合提供了支持,这些基因的表达与组织无关。我们评估了滞育与细胞周期停滞、发育停滞和应激耐受性增加有关的总体假设,并发现了TOR和胰岛素信号传导受到抑制、细胞周期活性降低以及通过热休克蛋白表达和细胞骨架重塑增加应激反应能力的证据。然而,这些过程因组织而异,在滞育期间,大脑和脂肪体似乎比中肠或马尔皮氏管保持更高水平的细胞活动。我们还观察到滞育维持期间基因表达的温度依赖性变化,特别是与热休克反应和MAPK、胰岛素和TOR信号通路相关的基因。此外,我们为滞育/滞育后静止过渡期间的表观遗传学重组以及参与翻译后修饰的基因的表达提供了证据,强调了研究这些候选基因和过程的蛋白质活性的必要性。我们得出的结论是,滞育的发育是通过不同的组织特异性基因表达谱来协调的,并且不同组织的典型滞育表型不同。
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
Current Research in Insect Science
Current Research in Insect Science Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
3.20
自引率
0.00%
发文量
22
审稿时长
36 days
×
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