MicroRNA control of stem cell reconstitution and growth in root regeneration

IF 15.8 1区 生物学 Q1 PLANT SCIENCES Nature Plants Pub Date : 2025-02-25 DOI:10.1038/s41477-025-01922-0
J. L. Baulies, R. E. Rodríguez, F. E. Lazzara, D. Liebsch, X. Zhao, J. Zeng, L. Bald, C. Schommer, J. U. Lohmann, J. F. Palatnik
{"title":"MicroRNA control of stem cell reconstitution and growth in root regeneration","authors":"J. L. Baulies, R. E. Rodríguez, F. E. Lazzara, D. Liebsch, X. Zhao, J. Zeng, L. Bald, C. Schommer, J. U. Lohmann, J. F. Palatnik","doi":"10.1038/s41477-025-01922-0","DOIUrl":null,"url":null,"abstract":"<p>Plants display a remarkable regeneration capacity, which allows them to replace damaged or lost cells, tissues and organs, and thus recover from a broad spectrum of injuries<sup>1,2</sup>. Even lost stem cells can be regenerated from non-stem cells after competence acquisition, highlighting the enormous plasticity of plant cells. However, the molecular mechanisms underlying this process are still poorly understood. In the root, the highly conserved microRNA miR396 and its targets, the <i>GROWTH-REGULATING FACTORs</i> (<i>GRFs</i>), control the transition from stem cells to proliferative cells. miR396 promotes stem cell activity by repressing and excluding the GRFs from the stem cell area. In turn, the GRFs promote cell division in the proliferation zone<sup>3</sup>. Here we show that the miR396–GRF regulatory module guides stem cell reconstitution after root tip excision, playing a dual role: while miR396 promotes competence, the GRFs control regeneration speed. Moreover, plants with ectopic miR396 expression have defined stem cell niches before the excision but do not reconstitute them afterwards, remaining in an open state despite continuing to grow. We propose that this phenomenon is caused by dispersed stem cell activity, which supports growth after root tip excision without reconstituting the organized and spatially restricted stem cell niche typical of <i>Arabidopsis</i> roots.</p>","PeriodicalId":18904,"journal":{"name":"Nature Plants","volume":"3 1","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41477-025-01922-0","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Plants display a remarkable regeneration capacity, which allows them to replace damaged or lost cells, tissues and organs, and thus recover from a broad spectrum of injuries1,2. Even lost stem cells can be regenerated from non-stem cells after competence acquisition, highlighting the enormous plasticity of plant cells. However, the molecular mechanisms underlying this process are still poorly understood. In the root, the highly conserved microRNA miR396 and its targets, the GROWTH-REGULATING FACTORs (GRFs), control the transition from stem cells to proliferative cells. miR396 promotes stem cell activity by repressing and excluding the GRFs from the stem cell area. In turn, the GRFs promote cell division in the proliferation zone3. Here we show that the miR396–GRF regulatory module guides stem cell reconstitution after root tip excision, playing a dual role: while miR396 promotes competence, the GRFs control regeneration speed. Moreover, plants with ectopic miR396 expression have defined stem cell niches before the excision but do not reconstitute them afterwards, remaining in an open state despite continuing to grow. We propose that this phenomenon is caused by dispersed stem cell activity, which supports growth after root tip excision without reconstituting the organized and spatially restricted stem cell niche typical of Arabidopsis roots.

Abstract Image

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
求助全文
约1分钟内获得全文 去求助
来源期刊
Nature Plants
Nature Plants PLANT SCIENCES-
CiteScore
25.30
自引率
2.20%
发文量
196
期刊介绍: Nature Plants is an online-only, monthly journal publishing the best research on plants — from their evolution, development, metabolism and environmental interactions to their societal significance.
期刊最新文献
BRUTUS links iron with legume–rhizobia symbiosis A microRNA defines root regeneration MADS31 supports female germline development by repressing the post-fertilization programme in cereal ovules MADS31 coordinates germline development in cereal ovules MicroRNA control of stem cell reconstitution and growth in root regeneration
×
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:481959085
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