Preparing for parenthood: molecular reprogramming precedes parenting in the burying beetle Nicrophorus vespilloides.

IF 2.8 2区 生物学 Q1 ZOOLOGY
Julius Rombach, Heiko Vogel, Sandra Steiger, Volker Nehring
{"title":"Preparing for parenthood: molecular reprogramming precedes parenting in the burying beetle Nicrophorus vespilloides.","authors":"Julius Rombach, Heiko Vogel, Sandra Steiger, Volker Nehring","doi":"10.1186/s12983-026-00615-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Subsocial insects transition from solitary to social behavior during reproduction. They engage in cooperative and parental care activities that increase their offspring's survival. Elucidating the molecular mechanisms underlying such social transitions is crucial for understanding the genetic basis of social behavior. Burying beetles reproduce on a nutritious yet ephemeral resource. They provide intensive pre-hatching care by burying and preparing a vertebrate carcass, and post-hatching care by feeding the larvae.</p><p><strong>Results: </strong>We analyzed female gene expression during the transition from solitary life to brood care in the subsocial burying beetle Nicrophorus vespilloides. We collected RNA-seq data from the heads and fat bodies of beetles at four different time points: solitary life, early pre-hatching care, late pre-hatching care, and post-hatching care. The most pronounced shift in gene expression occurred during the initial onset of social behavior. Carcass discovery caused massive changes in the transcription of genes involved in metabolism, translation, and immunity. Changes in gene expression between the different brood care phases were comparatively modest: Females upregulated the expression of genes associated with social immunity as parental care intensified. During brood care, they gradually downregulated fecundity-related genes.</p><p><strong>Conclusions: </strong>The regulatory pattern indicates that carcass discovery triggers an increased metabolism to cope with the demands of brood care, alongside a reduced investment in body maintenance. The overall regulatory pattern indicates a strong investment into the current reproduction bout at the expense of future reproduction.</p>","PeriodicalId":55142,"journal":{"name":"Frontiers in Zoology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2026-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13188450/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Zoology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12983-026-00615-4","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Subsocial insects transition from solitary to social behavior during reproduction. They engage in cooperative and parental care activities that increase their offspring's survival. Elucidating the molecular mechanisms underlying such social transitions is crucial for understanding the genetic basis of social behavior. Burying beetles reproduce on a nutritious yet ephemeral resource. They provide intensive pre-hatching care by burying and preparing a vertebrate carcass, and post-hatching care by feeding the larvae.

Results: We analyzed female gene expression during the transition from solitary life to brood care in the subsocial burying beetle Nicrophorus vespilloides. We collected RNA-seq data from the heads and fat bodies of beetles at four different time points: solitary life, early pre-hatching care, late pre-hatching care, and post-hatching care. The most pronounced shift in gene expression occurred during the initial onset of social behavior. Carcass discovery caused massive changes in the transcription of genes involved in metabolism, translation, and immunity. Changes in gene expression between the different brood care phases were comparatively modest: Females upregulated the expression of genes associated with social immunity as parental care intensified. During brood care, they gradually downregulated fecundity-related genes.

Conclusions: The regulatory pattern indicates that carcass discovery triggers an increased metabolism to cope with the demands of brood care, alongside a reduced investment in body maintenance. The overall regulatory pattern indicates a strong investment into the current reproduction bout at the expense of future reproduction.

为为人父母做准备:埋葬甲虫的分子重编程先于为人父母。
背景:亚社会性昆虫在繁殖过程中从独居行为转变为群居行为。它们参与合作和亲代照顾活动,以提高后代的存活率。阐明这种社会转变背后的分子机制对于理解社会行为的遗传基础至关重要。埋甲虫在营养丰富但短暂的资源上繁殖。他们通过掩埋和准备脊椎动物尸体来提供密集的孵化前护理,并通过喂养幼虫来提供孵化后护理。结果:我们分析了亚社会性埋葬甲虫从独居生活到育雏过程中雌性基因的表达。我们收集了4个不同时间点的甲虫头部和脂肪体的RNA-seq数据:独居生活、早期孵化前护理、后期孵化前护理和孵化后护理。最显著的基因表达变化发生在社会行为的初始阶段。尸体的发现引起了代谢、翻译和免疫相关基因转录的巨大变化。不同育雏阶段的基因表达变化相对温和:随着亲代抚育的加强,雌性上调与社会免疫相关的基因表达。在育雏过程中,它们逐渐下调与繁殖力相关的基因。结论:调节模式表明,胴体发现触发代谢增加以应对育雏需求,同时减少身体维护投资。总体调控模式表明,对当前繁殖回合的大力投资是以牺牲未来繁殖为代价的。
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
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life. As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem. Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost. The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.
×
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