Germline expression of Imp-L2 in Drosophila females enhances reproductive activity and longevity.

IF 3.2 2区 生物学 Q3 CELL BIOLOGY Animal Cells and Systems Pub Date : 2025-03-17 eCollection Date: 2025-01-01 DOI:10.1080/19768354.2025.2480150
Sujin Noh, Sungjoon Na, Xinge Song, Seogang Hyun
{"title":"Germline expression of Imp-L2 in Drosophila females enhances reproductive activity and longevity.","authors":"Sujin Noh, Sungjoon Na, Xinge Song, Seogang Hyun","doi":"10.1080/19768354.2025.2480150","DOIUrl":null,"url":null,"abstract":"<p><p>The Imaginal morphogenesis protein-Late 2 (Imp-L2) in <i>Drosophila</i> is recognized as a functional homolog of the insulin-like growth factor (IGF) binding protein family. In this study, we report that Imp-L2 expression in germline cells during oogenesis simultaneously enhances both fecundity and lifespan in female <i>Drosophila</i>. Loss of Imp-L2, either through knockout or germline-specific knockdown, resulted in decreased reproductive activity, as evidenced by reduced ovary size and fecundity, along with a higher proportion of infertile flies. Conversely, overexpression of Imp-L2 specifically in germline cells enhanced reproductive activity. Imp-L2 appears to regulate germline stem cell proliferation and differentiation independently of IGF signaling. Interestingly, germline-specific knockdown of <i>Imp-L2</i> shortened the lifespan of female flies, whereas its overexpression extended it. Thus, Imp-L2 expression in the germline promotes both reproductive activity and longevity, presenting an exception to the typical trade-off between reproduction and lifespan.</p>","PeriodicalId":7804,"journal":{"name":"Animal Cells and Systems","volume":"29 1","pages":"31-40"},"PeriodicalIF":3.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11915738/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Cells and Systems","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/19768354.2025.2480150","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The Imaginal morphogenesis protein-Late 2 (Imp-L2) in Drosophila is recognized as a functional homolog of the insulin-like growth factor (IGF) binding protein family. In this study, we report that Imp-L2 expression in germline cells during oogenesis simultaneously enhances both fecundity and lifespan in female Drosophila. Loss of Imp-L2, either through knockout or germline-specific knockdown, resulted in decreased reproductive activity, as evidenced by reduced ovary size and fecundity, along with a higher proportion of infertile flies. Conversely, overexpression of Imp-L2 specifically in germline cells enhanced reproductive activity. Imp-L2 appears to regulate germline stem cell proliferation and differentiation independently of IGF signaling. Interestingly, germline-specific knockdown of Imp-L2 shortened the lifespan of female flies, whereas its overexpression extended it. Thus, Imp-L2 expression in the germline promotes both reproductive activity and longevity, presenting an exception to the typical trade-off between reproduction and lifespan.

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
雌性果蝇种系表达Imp-L2可提高生殖活性和寿命。
果蝇的想象形态发生蛋白-晚2 (Imp-L2)被认为是胰岛素样生长因子(IGF)结合蛋白家族的功能同源物。在这项研究中,我们报道了在雌性果蝇的卵发生过程中,种系细胞中表达Imp-L2同时提高了繁殖力和寿命。无论是通过基因敲除还是种系特异性敲除,Imp-L2的缺失都会导致生殖活性下降,如卵巢大小和繁殖力的减少,以及不育苍蝇比例的增加。相反,在种系细胞中过表达Imp-L2可增强生殖活性。Imp-L2似乎独立于IGF信号传导调节种系干细胞的增殖和分化。有趣的是,种系特异性敲除Imp-L2会缩短雌性果蝇的寿命,而其过表达会延长雌性果蝇的寿命。因此,种系中Imp-L2的表达促进了生殖活动和寿命,这是繁殖和寿命之间典型权衡的一个例外。
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
Animal Cells and Systems
Animal Cells and Systems 生物-动物学
CiteScore
4.50
自引率
24.10%
发文量
33
审稿时长
6 months
期刊介绍: Animal Cells and Systems is the official journal of the Korean Society for Integrative Biology. This international, peer-reviewed journal publishes original papers that cover diverse aspects of biological sciences including Bioinformatics and Systems Biology, Developmental Biology, Evolution and Systematic Biology, Population Biology, & Animal Behaviour, Molecular and Cellular Biology, Neurobiology and Immunology, and Translational Medicine.
期刊最新文献
Tetramethylthiuram disulfide induces stress granules and DNA damage through oxidative stress in human lung epithelial cells. Integrated morphological and transcriptomic analysis of sucker development in Octopus minor. Notch signaling in leech neurogenesis: expression patterns and functional insights in the Glossiphoniid leech Helobdella austinensis. Long non-coding RNAs in the exosomal network: dual roles and clinical implications in cancer. From threatened to widespread: a non-genuine conservation status update for a now widespread Asian Hylid.
×
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:604180095
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