Photoperiod controls insulin and juvenile hormone signaling pathways via the circadian clock in the bean bug Riptortus pedestris (Hemiptera: Alydidae)

IF 1.3 4区 农林科学 Q2 ENTOMOLOGY Applied Entomology and Zoology Pub Date : 2022-08-21 DOI:10.1007/s13355-022-00795-5
Genyu Mano, Shin G. Goto
{"title":"Photoperiod controls insulin and juvenile hormone signaling pathways via the circadian clock in the bean bug Riptortus pedestris (Hemiptera: Alydidae)","authors":"Genyu Mano,&nbsp;Shin G. Goto","doi":"10.1007/s13355-022-00795-5","DOIUrl":null,"url":null,"abstract":"<div><p>Most multivoltine insects in temperate zones enter diapause in response to short days. The photoperiod is evaluated in these organisms by a photoperiodic time measurement system, which involves the circadian clock, and activates or inactivates endocrine organs or cells to alter their physiological status. Although the physiological mechanisms underlying insect photoperiodism have been extensively studied, the molecular linkage between the circadian clock and endocrine signaling pathways remains unclear. In this study, we evaluated the bean bug <i>Riptortus pedestris</i> (F.) (Hemiptera: Alydidae), which enters adult (reproductive) diapause in response to short days. A gene encoding the insulin-like peptide ILP1, which is expressed in the pars intercerebralis in the brain, was upregulated and involved in fecundity under long days. <i>Ilp1</i> appeared to function independently of the photoperiodic response controlled by juvenile hormone signaling. <i>Cyp15</i>, which encodes an epoxidase crucial for juvenile hormone biosynthesis, was upregulated and involved in ovarian development under long days. RNA interference targeted against the circadian clock gene <i>per</i> canceled the <i>Ilp1</i> and <i>Cyp15</i> suppression and allowed females to be reproductive even under diapause-inducing short days. Thus, the circadian clock may control the photoperiodic response by altering the expression of key elements in two independent endocrine pathways.</p></div>","PeriodicalId":8551,"journal":{"name":"Applied Entomology and Zoology","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2022-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Entomology and Zoology","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s13355-022-00795-5","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Most multivoltine insects in temperate zones enter diapause in response to short days. The photoperiod is evaluated in these organisms by a photoperiodic time measurement system, which involves the circadian clock, and activates or inactivates endocrine organs or cells to alter their physiological status. Although the physiological mechanisms underlying insect photoperiodism have been extensively studied, the molecular linkage between the circadian clock and endocrine signaling pathways remains unclear. In this study, we evaluated the bean bug Riptortus pedestris (F.) (Hemiptera: Alydidae), which enters adult (reproductive) diapause in response to short days. A gene encoding the insulin-like peptide ILP1, which is expressed in the pars intercerebralis in the brain, was upregulated and involved in fecundity under long days. Ilp1 appeared to function independently of the photoperiodic response controlled by juvenile hormone signaling. Cyp15, which encodes an epoxidase crucial for juvenile hormone biosynthesis, was upregulated and involved in ovarian development under long days. RNA interference targeted against the circadian clock gene per canceled the Ilp1 and Cyp15 suppression and allowed females to be reproductive even under diapause-inducing short days. Thus, the circadian clock may control the photoperiodic response by altering the expression of key elements in two independent endocrine pathways.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
光周期通过昼夜节律时钟控制豆虫Riptotus pedetris(半翅目:Alydidae)的胰岛素和幼激素信号通路
温带地区的多数多伏特昆虫由于白昼短而进入滞育。在这些生物体中,光周期通过光周期时间测量系统进行评估,该系统涉及昼夜节律钟,并激活或停用内分泌器官或细胞以改变其生理状态。尽管昆虫光周期的生理机制已被广泛研究,但生物钟与内分泌信号通路之间的分子联系尚不清楚。在本研究中,我们评价了在短日照条件下进入成虫(生殖)滞育的豆虫Riptortus pestris (F.)(半翅目:豆虫科)。一种编码胰岛素样肽ILP1的基因,在大脑的脑间部表达,在长时间的白天被上调并参与繁殖力。Ilp1似乎独立于由幼代激素信号控制的光周期反应发挥作用。Cyp15编码一种环氧酶,对青少年激素的生物合成至关重要,在长时间内上调并参与卵巢发育。针对生物钟基因的RNA干扰取消了Ilp1和Cyp15的抑制,使雌性即使在诱导滞育的短时间内也能繁殖。因此,生物钟可能通过改变两个独立内分泌通路中关键元素的表达来控制光周期反应。
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 去求助
来源期刊
CiteScore
2.70
自引率
7.70%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Applied Entomology and Zoology publishes articles concerned with applied entomology, applied zoology, agricultural chemicals and pest control in English. Contributions of a basic and fundamental nature may be accepted at the discretion of the Editor. Manuscripts of original research papers, technical notes and reviews are accepted for consideration. No manuscript that has been published elsewhere will be accepted for publication.
期刊最新文献
Control of the Japanese orange fly, Bactrocera tsuneonis (Diptera: Tephritidae), through several preharvest management practices: establishment of a phytosanitary measure for citrus fruits for export Effects of Alphacypermethrin selection on fitness traits of Culex quinquefasciatus (Diptera: Culicidae) Detection of bee viruses from Apis mellifera (Hymenoptera: Apidae) and Varroa destructor (Acari: Varroidae) in Japan Experimental parasitism of the parasitoid beetle Dastarcus longulus (Coleoptera: Bothrideridae) larvae on invasive longhorn beetle Apriona swainsoni (Coleoptera: Cerambycidae) larvae A new record of the fairyfly Cosmocomoidea tenuis (Hymenoptera: Mymaridae) from Japan, with notes on its host associations
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1