根帽细胞尸体的清除限制了拟南芥中微生物的定植。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2024-11-12 DOI:10.7554/eLife.96266
Nyasha Charura, Ernesto Llamas, Concetta De Quattro, David Vilchez, Moritz K Nowack, Alga Zuccaro
{"title":"根帽细胞尸体的清除限制了拟南芥中微生物的定植。","authors":"Nyasha Charura, Ernesto Llamas, Concetta De Quattro, David Vilchez, Moritz K Nowack, Alga Zuccaro","doi":"10.7554/eLife.96266","DOIUrl":null,"url":null,"abstract":"<p><p>Programmed cell death occurring during plant development (dPCD) is a fundamental process integral for plant growth and reproduction. Here, we investigate the connection between developmentally controlled PCD and fungal accommodation in <i>Arabidopsis thaliana</i> roots, focusing on the root cap-specific transcription factor ANAC033/SOMBRERO (SMB) and the senescence-associated nuclease BFN1. Mutations of both dPCD regulators increase colonization by the beneficial fungus <i>Serendipita indica</i>, primarily in the differentiation zone. <i>smb-3</i> mutants additionally exhibit hypercolonization around the meristematic zone and a delay of <i>S. indica</i>-induced root-growth promotion. This demonstrates that root cap dPCD and rapid post-mortem clearance of cellular corpses represent a physical defense mechanism restricting microbial invasion of the root. Additionally, reporter lines and transcriptional analysis revealed that <i>BFN1</i> expression is downregulated during <i>S. indica</i> colonization in mature root epidermal cells, suggesting a transcriptional control mechanism that facilitates the accommodation of beneficial microbes in the roots.</p>","PeriodicalId":11640,"journal":{"name":"eLife","volume":"13 ","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556792/pdf/","citationCount":"0","resultStr":"{\"title\":\"Root cap cell corpse clearance limits microbial colonization in <i>Arabidopsis thaliana</i>.\",\"authors\":\"Nyasha Charura, Ernesto Llamas, Concetta De Quattro, David Vilchez, Moritz K Nowack, Alga Zuccaro\",\"doi\":\"10.7554/eLife.96266\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Programmed cell death occurring during plant development (dPCD) is a fundamental process integral for plant growth and reproduction. Here, we investigate the connection between developmentally controlled PCD and fungal accommodation in <i>Arabidopsis thaliana</i> roots, focusing on the root cap-specific transcription factor ANAC033/SOMBRERO (SMB) and the senescence-associated nuclease BFN1. Mutations of both dPCD regulators increase colonization by the beneficial fungus <i>Serendipita indica</i>, primarily in the differentiation zone. <i>smb-3</i> mutants additionally exhibit hypercolonization around the meristematic zone and a delay of <i>S. indica</i>-induced root-growth promotion. This demonstrates that root cap dPCD and rapid post-mortem clearance of cellular corpses represent a physical defense mechanism restricting microbial invasion of the root. Additionally, reporter lines and transcriptional analysis revealed that <i>BFN1</i> expression is downregulated during <i>S. indica</i> colonization in mature root epidermal cells, suggesting a transcriptional control mechanism that facilitates the accommodation of beneficial microbes in the roots.</p>\",\"PeriodicalId\":11640,\"journal\":{\"name\":\"eLife\",\"volume\":\"13 \",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556792/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eLife\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.7554/eLife.96266\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7554/eLife.96266","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

植物发育过程中发生的程序性细胞死亡(dPCD)是植物生长和繁殖不可或缺的基本过程。在这里,我们研究了拟南芥根部发育控制的 PCD 与真菌宿主之间的联系,重点是根帽特异性转录因子 ANAC033/SOMBRERO (SMB) 和衰老相关核酸酶 BFN1。这两种 dPCD 调节因子的突变都增加了有益真菌 Serendipita indica 的定殖,主要是在分化区。smb-3 突变体还表现出分生区周围的过度定殖,以及 S. indica 诱导的根生长促进的延迟。这表明根帽 dPCD 和细胞尸体的快速死后清除代表了一种限制微生物入侵根部的物理防御机制。此外,报告基因和转录分析表明,在 S. indica 定殖期间,成熟根表皮细胞中的 BFN1 表达下调,这表明转录控制机制有利于有益微生物在根中的容纳。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Root cap cell corpse clearance limits microbial colonization in Arabidopsis thaliana.

Programmed cell death occurring during plant development (dPCD) is a fundamental process integral for plant growth and reproduction. Here, we investigate the connection between developmentally controlled PCD and fungal accommodation in Arabidopsis thaliana roots, focusing on the root cap-specific transcription factor ANAC033/SOMBRERO (SMB) and the senescence-associated nuclease BFN1. Mutations of both dPCD regulators increase colonization by the beneficial fungus Serendipita indica, primarily in the differentiation zone. smb-3 mutants additionally exhibit hypercolonization around the meristematic zone and a delay of S. indica-induced root-growth promotion. This demonstrates that root cap dPCD and rapid post-mortem clearance of cellular corpses represent a physical defense mechanism restricting microbial invasion of the root. Additionally, reporter lines and transcriptional analysis revealed that BFN1 expression is downregulated during S. indica colonization in mature root epidermal cells, suggesting a transcriptional control mechanism that facilitates the accommodation of beneficial microbes in the roots.

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
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
×
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