Sex-specific chemosensory gene expression in the whitelined sphinx moth (Lepidoptera: Hyles lineata) suggests a role for odorant-binding proteins in host plant choice

R Keating Godfrey, Anthony Auletta, Edison Cheung, Riley M. Harper, Kireina Kates, Akito Y Kawahara, Yichen Li, Cristina Mercado, Fernando Miguelena, Ginger Pickett, Peter DiGennaro
{"title":"Sex-specific chemosensory gene expression in the whitelined sphinx moth (Lepidoptera: Hyles lineata) suggests a role for odorant-binding proteins in host plant choice","authors":"R Keating Godfrey, Anthony Auletta, Edison Cheung, Riley M. Harper, Kireina Kates, Akito Y Kawahara, Yichen Li, Cristina Mercado, Fernando Miguelena, Ginger Pickett, Peter DiGennaro","doi":"10.1101/2024.09.04.611314","DOIUrl":null,"url":null,"abstract":"The whitelined sphinx moth, Hyles lineata, is a generalist during both the larval and adult stages with a broad geographic range extending across North and Central America. Within the genus Hyles there have been multiple transitions to a narrower host plant range, making Hyles an ideal group to study the evolution and mechanisms of host plant selection. We characterize sex- and appendage-specific chemosensory gene expression in H. lineata, the oldest extant member of the genus. We also describe female-specific gene expression in appendages used to sense plant surfaces as a means of identifying candidate genes involved in host plant choice. Sensilla on these appendages house sensory neurons and support cells that express chemosensory genes, receptors, and small proteins that bind, shuttle, and transport small molecules to allow detection of odorants and other small molecules. We considered genes detected more frequently in the female leg and ovipositor samples to be candidate oviposition-relevant genes. Most chemosensory genes of interest were detected in both sexes, while several odorant receptors were only detected in females. We identified 18 putative chemosensory genes that were specific to female legs, ovipositors, or both body parts. However, most of these genes did not reach statistical criteria to be considered differentially expressed. Instead, a set of OBPs show statistically significant female-biased expression in legs and ovipositors. These genes may serve as candidates for future study of the evolution and mechanisms of oviposition behavior in this species and its relatives.","PeriodicalId":501183,"journal":{"name":"bioRxiv - Evolutionary Biology","volume":"67 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Evolutionary Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.04.611314","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The whitelined sphinx moth, Hyles lineata, is a generalist during both the larval and adult stages with a broad geographic range extending across North and Central America. Within the genus Hyles there have been multiple transitions to a narrower host plant range, making Hyles an ideal group to study the evolution and mechanisms of host plant selection. We characterize sex- and appendage-specific chemosensory gene expression in H. lineata, the oldest extant member of the genus. We also describe female-specific gene expression in appendages used to sense plant surfaces as a means of identifying candidate genes involved in host plant choice. Sensilla on these appendages house sensory neurons and support cells that express chemosensory genes, receptors, and small proteins that bind, shuttle, and transport small molecules to allow detection of odorants and other small molecules. We considered genes detected more frequently in the female leg and ovipositor samples to be candidate oviposition-relevant genes. Most chemosensory genes of interest were detected in both sexes, while several odorant receptors were only detected in females. We identified 18 putative chemosensory genes that were specific to female legs, ovipositors, or both body parts. However, most of these genes did not reach statistical criteria to be considered differentially expressed. Instead, a set of OBPs show statistically significant female-biased expression in legs and ovipositors. These genes may serve as candidates for future study of the evolution and mechanisms of oviposition behavior in this species and its relatives.
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
白纹狮身蛾(鳞翅目:Hyles lineata)的性别特异性化感基因表达表明气味结合蛋白在寄主植物选择中的作用
白刺蛾(Hyles lineata)在幼虫期和成虫期都是一种通食植物,其地理分布广泛,横跨北美洲和中美洲。在海尔斯蛾属中,寄主植物范围曾多次缩小,这使得海尔斯蛾成为研究寄主植物选择的进化和机制的理想类群。我们描述了该属现存最古老成员 H. lineata 的性别和附属器官特异性化感基因表达。我们还描述了用于感知植物表面的附肢中雌性特异性基因的表达,以此来确定参与寄主植物选择的候选基因。这些附肢上的感觉器容纳了感觉神经元和支持细胞,它们表达化学感觉基因、受体和小蛋白,这些基因、受体和小蛋白能结合、穿梭和运输小分子,从而检测气味和其他小分子。我们认为,在雌性腿部和产卵器样本中检测到的频率较高的基因是与排卵相关的候选基因。大多数感兴趣的化感基因在雌雄昆虫中都能检测到,而一些气味受体只在雌性昆虫中检测到。我们发现了 18 个对雌性腿部、产卵器或两个身体部位都有特异性的假定化感基因。然而,这些基因中的大多数都没有达到统计学标准,不能被认为是差异表达基因。相反,一组 OBPs 在腿部和产卵器中显示出显著的雌性偏向表达。这些基因可作为未来研究该物种及其近缘种产卵行为的进化和机制的候选基因。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Conserved Evolutionary Response to Whole Genome Duplication in Angiosperms Revealed Using High Resolution Gene Expression Profiling Adaptation to climate in the native and introduced ranges of a cosmopolitan plant Ecotype formation in the European anchovy fuelled by structural variants of different origins and genetic interactions with a southern lineage Most Beefalo cattle have no detectable bison genetic ancestry An Experimental Test of Local Adaptation in Native and Introduced Populations of an Ectomycorrhizal Fungus, Suillus luteus
×
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