CRY1 is involved in the take-off behaviour of migratory Cnaphalocrocis medinalis individuals.

IF 4.4 1区 生物学 Q1 BIOLOGY
Tianyi Sun, Fan Yang, Haiyan Zhang, Yajun Yang, Zhongxian Lu, Baoping Zhai, Hongxing Xu, Jiahao Lu, Yanhui Lu, Yumeng Wang, Jiawen Guo, Gao Hu
{"title":"CRY1 is involved in the take-off behaviour of migratory Cnaphalocrocis medinalis individuals.","authors":"Tianyi Sun, Fan Yang, Haiyan Zhang, Yajun Yang, Zhongxian Lu, Baoping Zhai, Hongxing Xu, Jiahao Lu, Yanhui Lu, Yumeng Wang, Jiawen Guo, Gao Hu","doi":"10.1186/s12915-024-01964-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Numerous insect species undertake long-distance migrations on an enormous scale, with great implications for ecosystems. Given that take-off is the point where it all starts, whether and how the external light and internal circadian rhythm are involved in regulating the take-off behaviour remains largely unknown. Herein, we explore this issue in a migratory pest, Cnaphalocrocis medinalis, via behavioural observations and RNAi experiments.</p><p><strong>Results: </strong>The results showed that C. medinalis moths took off under conditions where the light intensity gradually weakened to 0.1 lx during the afternoon or evening, and the take-off proportions under full spectrum or blue light were significantly higher than that under red and green light. The ultraviolet-A/blue light-sensitive type 1 cryptochrome gene (Cmedcry1) was significantly higher in take-off moths than that of non-take-off moths. In contrast, the expression of the light-insensitive CRY2 (Cmedcry2) and circadian genes (Cmedtim and Cmedper) showed no significant differences. After silencing Cmedcry1, the take-off proportion significantly decreased. Thus, Cmedcry1 is involved in the decrease in light intensity induced take-off behaviour in C. medinalis.</p><p><strong>Conclusions: </strong>This study can help further explain the molecular mechanisms behind insect migration, especially light perception and signal transmission during take-off phases.</p>","PeriodicalId":9339,"journal":{"name":"BMC Biology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11320853/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12915-024-01964-4","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Numerous insect species undertake long-distance migrations on an enormous scale, with great implications for ecosystems. Given that take-off is the point where it all starts, whether and how the external light and internal circadian rhythm are involved in regulating the take-off behaviour remains largely unknown. Herein, we explore this issue in a migratory pest, Cnaphalocrocis medinalis, via behavioural observations and RNAi experiments.

Results: The results showed that C. medinalis moths took off under conditions where the light intensity gradually weakened to 0.1 lx during the afternoon or evening, and the take-off proportions under full spectrum or blue light were significantly higher than that under red and green light. The ultraviolet-A/blue light-sensitive type 1 cryptochrome gene (Cmedcry1) was significantly higher in take-off moths than that of non-take-off moths. In contrast, the expression of the light-insensitive CRY2 (Cmedcry2) and circadian genes (Cmedtim and Cmedper) showed no significant differences. After silencing Cmedcry1, the take-off proportion significantly decreased. Thus, Cmedcry1 is involved in the decrease in light intensity induced take-off behaviour in C. medinalis.

Conclusions: This study can help further explain the molecular mechanisms behind insect migration, especially light perception and signal transmission during take-off phases.

CRY1参与了medinalis迁徙个体的起飞行为。
背景:许多昆虫物种都进行过大规模的长途迁徙,对生态系统产生了重大影响。鉴于起飞是一切的起点,外部光照和内部昼夜节律是否以及如何参与调节起飞行为在很大程度上仍是未知数。在此,我们通过行为观察和 RNAi 实验,在迁徙性害虫褐飞虱中探讨了这一问题:结果表明:在下午或傍晚光照强度逐渐减弱至0.1 lx的条件下,C. medinalis蛾起飞,全光谱或蓝光下的起飞比例明显高于红光和绿光下的起飞比例。起飞蛾对紫外线-A/蓝光敏感的 1 型隐色基因(Cmedcry1)的表达量明显高于未起飞蛾。相比之下,对光不敏感的 CRY2(Cmedcry2)和昼夜节律基因(Cmedtim 和 Cmedper)的表达则没有明显差异。沉默 Cmedcry1 后,起飞比例明显下降。因此,Cmedcry1 参与了光照强度降低诱导的鳉鱼起飞行为:这项研究有助于进一步解释昆虫迁徙背后的分子机制,尤其是起飞阶段的光感知和信号传递。
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
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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