• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

幼虫期蜂王卵巢中生殖细胞前体的发育。

Development of germline progenitors in larval queen honeybee ovaries.

机构信息

Genomics Aotearoa, Bioprotection Aotearoa and Biochemistry Department, University of Otago, Dunedin 9016, Aotearoa, New Zealand.

出版信息

Biol Open. 2024 Sep 15;13(9). doi: 10.1242/bio.060511. Epub 2024 Sep 12.

DOI:10.1242/bio.060511
PMID:39263864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11413931/
Abstract

Honeybees (Apis mellifera) are a keystone species for managed pollination and the production of hive products. Eusociality in honeybees leads to much of the reproduction in a hive driven by the queen. Queen bees have two large active ovaries that can produce large numbers of eggs if conditions are appropriate. These ovaries are also active throughout the long lives of these insects, up to 5 years in some cases. Recent studies have indicated that the germline precursors of the adult honeybee queen ovary are organized into 8-cell clusters, joined together by a polyfusome; a cytoplasmic bridge. To understand the origin of these clusters, and trace the development of the honeybee queen ovary, we examined the cell types and regionalization of the developing larval and pupal queen ovaries. We used established (nanos and castor), and novel (odd skipped) gene expression markers to determine regions of the developing ovary. Primordial germline cells develop in the honeybee embryo and are organized into ovary structures before the embryo hatches. The ovary is regionalized by larval stage 3 into terminal filaments and germaria. At this stage, clusters of germline cells in the germaria are joined by fusomes and are dividing synchronously. The origin of the 8-cell clusters in the adult germarium is therefore during larval stages. On emergence, the queen ovary has terminal filaments and germaria but has not yet developed any vitellaria, which are produced after the queen embarks on a nuptial flight. The lack of germaria, and the storing of germline progenitors as clusters, may be adaptions for queen bees to endure the metabolic demands of a nuptial flight, as well as rapidly lay large numbers of eggs to establish a hive.

摘要

蜜蜂(Apis mellifera)是管理授粉和蜂产品生产的关键物种。蜜蜂的群居导致了蜂巢中大部分的繁殖活动由蜂王驱动。蜂王有两个大的活跃卵巢,如果条件合适,它们可以产生大量的卵子。这些卵巢在这些昆虫的长寿命中也保持活跃,在某些情况下长达 5 年。最近的研究表明,成年蜂王卵巢的生殖系前体细胞组织成 8 个细胞簇,通过多丝体连接在一起;细胞质桥。为了了解这些簇的起源,并追踪蜂王卵巢的发育,我们检查了幼虫和蛹期蜂王卵巢的细胞类型和区域化。我们使用了已建立的(nanos 和 castor)和新的(odd skipped)基因表达标记来确定卵巢发育的区域。原始生殖细胞在蜜蜂胚胎中发育,并在胚胎孵化前组织成卵巢结构。卵巢在幼虫阶段 3 时通过末端丝和生殖腺进行区域化。在这个阶段,生殖腺中的生殖细胞簇通过丝体连接并同步分裂。因此,成虫生殖腺中的 8 个细胞簇起源于幼虫阶段。在成虫出现时,蜂王卵巢具有末端丝和生殖腺,但尚未发育任何卵黄体,卵黄体是在蜂王开始婚飞后产生的。生殖腺的缺乏以及生殖系祖细胞以簇的形式储存,可能是蜂王适应婚飞代谢需求以及快速产卵以建立蜂巢的适应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/eb1fe4837fbf/biolopen-13-060511-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/29a1faf13bdc/biolopen-13-060511-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/fb13f3fcd06d/biolopen-13-060511-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/5168a1a53a98/biolopen-13-060511-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/3e10d7985b7c/biolopen-13-060511-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/74b4651eefc8/biolopen-13-060511-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/12b70a8a76a8/biolopen-13-060511-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/7c0f38c66988/biolopen-13-060511-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/eb1fe4837fbf/biolopen-13-060511-g8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/29a1faf13bdc/biolopen-13-060511-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/fb13f3fcd06d/biolopen-13-060511-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/5168a1a53a98/biolopen-13-060511-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/3e10d7985b7c/biolopen-13-060511-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/74b4651eefc8/biolopen-13-060511-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/12b70a8a76a8/biolopen-13-060511-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/7c0f38c66988/biolopen-13-060511-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0566/11413931/eb1fe4837fbf/biolopen-13-060511-g8.jpg

相似文献

1
Development of germline progenitors in larval queen honeybee ovaries.幼虫期蜂王卵巢中生殖细胞前体的发育。
Biol Open. 2024 Sep 15;13(9). doi: 10.1242/bio.060511. Epub 2024 Sep 12.
2
Germline progenitors and oocyte production in the honeybee queen ovary.蜂王卵巢中的生殖系祖细胞和卵母细胞发生。
Genetics. 2023 Aug 31;225(1). doi: 10.1093/genetics/iyad138.
3
Dimorphic ovary differentiation in honeybee (Apis mellifera) larvae involves caste-specific expression of homologs of ark and buffy cell death genes.蜜蜂(西方蜜蜂)幼虫的二态卵巢分化涉及ark和buffy细胞死亡基因同源物的种型特异性表达。
PLoS One. 2014 May 20;9(5):e98088. doi: 10.1371/journal.pone.0098088. eCollection 2014.
4
Mating status and the evolution of eusociality: Oogenesis is independent of mating status in the solitary bee Osmia bicornis.交配状态与社会性的进化:孤雌生殖在独居熊蜂 Osmia bicornis 中与交配状态无关。
J Insect Physiol. 2020 Feb-Mar;121:104003. doi: 10.1016/j.jinsphys.2019.104003. Epub 2019 Dec 26.
5
Notch signalling mediates reproductive constraint in the adult worker honeybee.Notch 信号通路介导了成年工蜂的生殖限制。
Nat Commun. 2016 Aug 3;7:12427. doi: 10.1038/ncomms12427.
6
MicroRNA signatures characterizing caste-independent ovarian activity in queen and worker honeybees (Apis mellifera L.).表征蜂王和工蜂(西方蜜蜂)种型无关卵巢活性的微小RNA特征。
Insect Mol Biol. 2016 Jun;25(3):216-26. doi: 10.1111/imb.12214. Epub 2016 Feb 8.
7
The pheromones of laying workers in two honeybee sister species: Apis cerana and Apis mellifera.两种蜜蜂姐妹种:中华蜜蜂和西方蜜蜂中产卵工蜂的信息素。
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2012 Apr;198(4):319-23. doi: 10.1007/s00359-012-0710-9. Epub 2012 Jan 18.
8
The molecular basis of socially induced egg-size plasticity in honey bees.社会性诱导蜜蜂卵大小可塑性的分子基础。
Elife. 2022 Nov 8;11:e80499. doi: 10.7554/eLife.80499.
9
Mitochondrial proteins differential expression during honeybee (Apis mellifera L.) queen and worker larvae caste determination.蜂王和工蜂幼虫品级决定过程中线粒体蛋白的差异表达。
J Proteome Res. 2011 Sep 2;10(9):4263-80. doi: 10.1021/pr200473a. Epub 2011 Aug 3.
10
Lethal fighting between honeybee queens and parasitic workers (Apis mellifera).蜜蜂蜂王与寄生工蜂(西方蜜蜂)之间的致命争斗。
Naturwissenschaften. 2003 Aug;90(8):378-81. doi: 10.1007/s00114-003-0445-0. Epub 2003 Jul 18.

引用本文的文献

1
The Drosophila ovarian terminal filament imports molecules needed to produce lipid droplets, the fusome, and functional germ cells.果蝇卵巢末端丝导入产生脂滴、纺锤体和功能性生殖细胞所需的分子。
bioRxiv. 2025 Jul 31:2025.07.30.667757. doi: 10.1101/2025.07.30.667757.

本文引用的文献

1
A scoping review on the effects of Varroa mite (Varroa destructor) on global honey bee decline.一项关于瓦螨(Varroa destructor)对全球蜜蜂减少影响的范围综述。
Sci Total Environ. 2024 Jan 1;906:167492. doi: 10.1016/j.scitotenv.2023.167492. Epub 2023 Sep 29.
2
Germline progenitors and oocyte production in the honeybee queen ovary.蜂王卵巢中的生殖系祖细胞和卵母细胞发生。
Genetics. 2023 Aug 31;225(1). doi: 10.1093/genetics/iyad138.
3
The Nasonia pair-rule gene regulatory network retains its function over 300 million years of evolution.
Nasonia 配对规则基因调控网络在 3 亿多年的进化中保留了其功能。
Development. 2022 Mar 1;149(5). doi: 10.1242/dev.199632. Epub 2022 Mar 9.
4
Reproductive plasticity and oogenesis in the queen honey bee (Apis mellifera).蜂王(Apis mellifera)的生殖可塑性和卵子发生。
J Insect Physiol. 2022 Jan;136:104347. doi: 10.1016/j.jinsphys.2021.104347. Epub 2021 Dec 10.
5
Past insecticide exposure reduces bee reproduction and population growth rate.过去接触杀虫剂会降低蜜蜂的繁殖能力和种群增长率。
Proc Natl Acad Sci U S A. 2021 Nov 30;118(48). doi: 10.1073/pnas.2109909118.
6
Overview of Bee Pollination and Its Economic Value for Crop Production.蜜蜂授粉概述及其对作物生产的经济价值。
Insects. 2021 Jul 31;12(8):688. doi: 10.3390/insects12080688.
7
Repeated loss of variation in insect ovary morphology highlights the role of development in life-history evolution.昆虫卵巢形态变异的反复丧失凸显了发育在生活史进化中的作用。
Proc Biol Sci. 2021 May 12;288(1950):20210150. doi: 10.1098/rspb.2021.0150. Epub 2021 May 5.
8
The importance of controlled mating in honeybee breeding.控制交配在蜜蜂养殖中的重要性。
Genet Sel Evol. 2019 Dec 12;51(1):74. doi: 10.1186/s12711-019-0518-y.
9
Quantifying the effects of pollen nutrition on honey bee queen egg laying with a new laboratory system.利用新的实验室系统量化花粉营养对蜜蜂蜂王产卵的影响。
PLoS One. 2018 Sep 5;13(9):e0203444. doi: 10.1371/journal.pone.0203444. eCollection 2018.
10
Ecological and evolutionary approaches to managing honeybee disease.管理蜜蜂疾病的生态和进化方法。
Nat Ecol Evol. 2017 Sep;1(9):1250-1262. doi: 10.1038/s41559-017-0246-z. Epub 2017 Aug 22.