自噬调节拟南芥雄配子体的繁殖力并控制肌动蛋白组织

IF 14.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
He Yan, Zhen Lu, Xiaojuan Du, Zhengtao You, Mingkang Yang, Nianle Li, Xuequan Li, Zailue Ni, Hong Wu, Xiangfeng Wang, Lifeng Zhao, Hao Wang
{"title":"自噬调节拟南芥雄配子体的繁殖力并控制肌动蛋白组织","authors":"He Yan, Zhen Lu, Xiaojuan Du, Zhengtao You, Mingkang Yang, Nianle Li, Xuequan Li, Zailue Ni, Hong Wu, Xiangfeng Wang, Lifeng Zhao, Hao Wang","doi":"10.1038/s41467-024-54468-8","DOIUrl":null,"url":null,"abstract":"<p>Autophagy, a crucial mechanism for cellular degradation, is regulated by conserved autophagy-related (ATG) core proteins across species. Impairments in autophagy result in significant developmental and reproductive aberrations in mammals. However, autophagy is thought to be functionally dispensable in <i>Arabidopsis thaliana</i> since most of the ATG mutants lack severe growth and reproductive defects. Here, we challenge this perception by unveiling a role for autophagy in male gametophyte development and fertility in Arabidopsis. A detailed re-assessment of <i>atg5</i> and <i>atg7</i> mutants found that reduced autophagy activity in germinated pollen accompanied by partial aberrations in sperm cell biogenesis and pollen tube growth, leading to compromised seed formation. Furthermore, we revealed autophagy modulates the spatial organization of actin filaments <i>via</i> targeted degradation of actin depolymerization factors ADF7 and Profilin2 in pollen grains and tubes through a key receptor, Neighbor of BRCA1 (NBR1). Our findings advance the understanding of the evolutionary conservation and diversification of autophagy in modulating male fertility in plants contrasting to mammals.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"1 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Autophagy modulates Arabidopsis male gametophyte fertility and controls actin organization\",\"authors\":\"He Yan, Zhen Lu, Xiaojuan Du, Zhengtao You, Mingkang Yang, Nianle Li, Xuequan Li, Zailue Ni, Hong Wu, Xiangfeng Wang, Lifeng Zhao, Hao Wang\",\"doi\":\"10.1038/s41467-024-54468-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Autophagy, a crucial mechanism for cellular degradation, is regulated by conserved autophagy-related (ATG) core proteins across species. Impairments in autophagy result in significant developmental and reproductive aberrations in mammals. However, autophagy is thought to be functionally dispensable in <i>Arabidopsis thaliana</i> since most of the ATG mutants lack severe growth and reproductive defects. Here, we challenge this perception by unveiling a role for autophagy in male gametophyte development and fertility in Arabidopsis. A detailed re-assessment of <i>atg5</i> and <i>atg7</i> mutants found that reduced autophagy activity in germinated pollen accompanied by partial aberrations in sperm cell biogenesis and pollen tube growth, leading to compromised seed formation. Furthermore, we revealed autophagy modulates the spatial organization of actin filaments <i>via</i> targeted degradation of actin depolymerization factors ADF7 and Profilin2 in pollen grains and tubes through a key receptor, Neighbor of BRCA1 (NBR1). Our findings advance the understanding of the evolutionary conservation and diversification of autophagy in modulating male fertility in plants contrasting to mammals.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":14.7000,\"publicationDate\":\"2024-11-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-024-54468-8\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-024-54468-8","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

自噬是一种重要的细胞降解机制,受不同物种中保守的自噬相关(ATG)核心蛋白调控。自噬功能受损会导致哺乳动物出现严重的发育和生殖畸变。然而,自噬在拟南芥中被认为在功能上是可有可无的,因为大多数 ATG 突变体都没有严重的生长和生殖缺陷。在这里,我们揭示了自噬在拟南芥雄配子体发育和生育中的作用,从而对这种看法提出了挑战。对 atg5 和 atg7 突变体的详细再评估发现,发芽花粉中自噬活性的降低伴随着精子细胞生物发生和花粉管生长的部分畸变,导致种子形成受到影响。此外,我们还发现自噬通过一个关键受体--BRCA1的邻居(NBR1),在花粉粒和花粉管中靶向降解肌动蛋白解聚因子ADF7和Profilin2,从而调节肌动蛋白丝的空间组织。我们的发现加深了人们对自噬在调节植物雄性生殖力方面的进化保护和多样性的理解,这与哺乳动物形成了鲜明对比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Autophagy modulates Arabidopsis male gametophyte fertility and controls actin organization

Autophagy modulates Arabidopsis male gametophyte fertility and controls actin organization

Autophagy, a crucial mechanism for cellular degradation, is regulated by conserved autophagy-related (ATG) core proteins across species. Impairments in autophagy result in significant developmental and reproductive aberrations in mammals. However, autophagy is thought to be functionally dispensable in Arabidopsis thaliana since most of the ATG mutants lack severe growth and reproductive defects. Here, we challenge this perception by unveiling a role for autophagy in male gametophyte development and fertility in Arabidopsis. A detailed re-assessment of atg5 and atg7 mutants found that reduced autophagy activity in germinated pollen accompanied by partial aberrations in sperm cell biogenesis and pollen tube growth, leading to compromised seed formation. Furthermore, we revealed autophagy modulates the spatial organization of actin filaments via targeted degradation of actin depolymerization factors ADF7 and Profilin2 in pollen grains and tubes through a key receptor, Neighbor of BRCA1 (NBR1). Our findings advance the understanding of the evolutionary conservation and diversification of autophagy in modulating male fertility in plants contrasting to mammals.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
×
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