HaJAK2/STAT5B Mediate the Post-Mating Switch of Reproductive Behaviour in Helicoverpa armigera Female

IF 1.8 3区 农林科学 Q2 ENTOMOLOGY
Journal of Applied Entomology Pub Date : 2026-04-01 Epub Date: 2026-01-02 DOI:10.1111/jen.70058
Yilin Wang, Zhixian Zhang, Xueyi Ruan, Xiaoxia Liu, Songdou Zhang
{"title":"HaJAK2/STAT5B Mediate the Post-Mating Switch of Reproductive Behaviour in Helicoverpa armigera Female","authors":"Yilin Wang,&nbsp;Zhixian Zhang,&nbsp;Xueyi Ruan,&nbsp;Xiaoxia Liu,&nbsp;Songdou Zhang","doi":"10.1111/jen.70058","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Mated female moths display behavioural and physiological changes such as oviposition initiation, reduced receptivity and shortened lifespan. The behavioural transition in post-mating female insects constitutes a critical adaptive strategy for optimising reproductive success, but little is known about the detailed regulatory molecules. The JAK/STAT signalling pathway has been confirmed to play an important role in insect cell growth, immunity and reproductive processes, but its potential role in post-mating behavioural transformation is still unclear. In this study, we initially identified core components of the JAK/STAT signalling pathway, <i>HaJAK2</i> and <i>HaSTAT5B</i>, in <i>Helicoverpa armigera</i> through screening of the NCBI database and transcriptomic data. Then phylogenetic analysis and multiple amino acid sequence alignment revealed high homology of HaJAK2 and HaSTAT5B with homologues of <i>Spodoptera litura</i> and <i>Helicoverpa zea</i>, respectively. QRT-PCR analysis demonstrated tissue-specific expression patterns of <i>HaJAK2</i> and <i>HaSTAT5B</i>, showing predominant expression in the spermathecae/parovaria tissue. Furthermore, RNAi-mediated gene knockdown experiments indicated that suppressing <i>HaJAK2</i> and <i>HaSTAT5B</i> expression altered post-mating behaviours, including reduced oviposition, extended longevity and diminished re-mating propensity. Finally, we revealed that the transcription factor <i>HaGATAa</i> dynamically regulates the expression of <i>HaJAK2</i> and <i>HaSTAT5B</i>. In conclusion, this study reveals that the GATAa-JAK/STAT axis governs reproductive state-dependent behavioural transitions in lepidopteran post-mating processes, advancing our understanding of insect reproductive strategies and identifying the JAK/STAT cascade as a potential target for novel pest control interventions to disrupt key reproductive behaviours in agricultural pests.</p>\n </div>","PeriodicalId":14987,"journal":{"name":"Journal of Applied Entomology","volume":"150 4","pages":"506-515"},"PeriodicalIF":1.8000,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Entomology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jen.70058","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/2 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Mated female moths display behavioural and physiological changes such as oviposition initiation, reduced receptivity and shortened lifespan. The behavioural transition in post-mating female insects constitutes a critical adaptive strategy for optimising reproductive success, but little is known about the detailed regulatory molecules. The JAK/STAT signalling pathway has been confirmed to play an important role in insect cell growth, immunity and reproductive processes, but its potential role in post-mating behavioural transformation is still unclear. In this study, we initially identified core components of the JAK/STAT signalling pathway, HaJAK2 and HaSTAT5B, in Helicoverpa armigera through screening of the NCBI database and transcriptomic data. Then phylogenetic analysis and multiple amino acid sequence alignment revealed high homology of HaJAK2 and HaSTAT5B with homologues of Spodoptera litura and Helicoverpa zea, respectively. QRT-PCR analysis demonstrated tissue-specific expression patterns of HaJAK2 and HaSTAT5B, showing predominant expression in the spermathecae/parovaria tissue. Furthermore, RNAi-mediated gene knockdown experiments indicated that suppressing HaJAK2 and HaSTAT5B expression altered post-mating behaviours, including reduced oviposition, extended longevity and diminished re-mating propensity. Finally, we revealed that the transcription factor HaGATAa dynamically regulates the expression of HaJAK2 and HaSTAT5B. In conclusion, this study reveals that the GATAa-JAK/STAT axis governs reproductive state-dependent behavioural transitions in lepidopteran post-mating processes, advancing our understanding of insect reproductive strategies and identifying the JAK/STAT cascade as a potential target for novel pest control interventions to disrupt key reproductive behaviours in agricultural pests.

HaJAK2/STAT5B介导棉铃虫雌性交配后生殖行为的转换
交配后的雌蛾表现出产卵开始、接受性降低和寿命缩短等行为和生理变化。交配后雌性昆虫的行为转变构成了优化繁殖成功的关键适应策略,但对详细的调节分子知之甚少。JAK/STAT信号通路已被证实在昆虫细胞生长、免疫和生殖过程中发挥重要作用,但其在交配后行为转变中的潜在作用尚不清楚。在本研究中,我们通过筛选NCBI数据库和转录组学数据,初步确定了棉铃虫JAK/STAT信号通路的核心组分HaJAK2和HaSTAT5B。系统发育分析和多氨基酸序列比对显示,HaJAK2和HaSTAT5B基因分别与斜纹夜蛾(Spodoptera litura)和玉米螺旋虫(Helicoverpa zea)的同源基因高度同源。QRT-PCR分析显示HaJAK2和HaSTAT5B具有组织特异性表达模式,主要表达于精囊/子宫颈组织。此外,rnai介导的基因敲低实验表明,抑制HaJAK2和HaSTAT5B的表达会改变交配后的行为,包括产卵减少、寿命延长和再交配倾向降低。最后,我们发现转录因子HaGATAa动态调控HaJAK2和HaSTAT5B的表达。总之,本研究揭示了GATAa-JAK/STAT轴控制鳞翅目交配后生殖状态依赖的行为转变,促进了我们对昆虫生殖策略的理解,并将JAK/STAT级联确定为新型害虫防治干预措施的潜在目标,以破坏农业害虫的关键生殖行为。
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
3.40
自引率
5.30%
发文量
132
审稿时长
6 months
期刊介绍: The Journal of Applied Entomology publishes original articles on current research in applied entomology, including mites and spiders in terrestrial ecosystems. Submit your next manuscript for rapid publication: the average time is currently 6 months from submission to publication. With Journal of Applied Entomology''s dynamic article-by-article publication process, Early View, fully peer-reviewed and type-set articles are published online as soon as they complete, without waiting for full issue compilation.
×
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:604180095
Book学术官方微信
小红书