• 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

盐诱导的根冠比变化中的自然变异揭示了SR3G作为拟南芥根木栓化和耐盐性的负调控因子。 (注:原文中“in.”应该是不完整信息,推测补充为“in Arabidopsis thaliana”进行了完整翻译,具体需结合完整原文判断 )

Natural variation in salt-induced changes in root:shoot ratio reveals SR3G as a negative regulator of root suberization and salt resilience in .

作者信息

Rahmati Ishka Maryam, Sussman Hayley, Hu Yunfei, Alqahtani Mashael Daghash, Craft Eric, Sicat Ronell, Wang Minmin, Yu Li'ang, Ait-Haddou Rachid, Li Bo, Drakakaki Georgia, Nelson Andrew D L, Pineros Miguel, Korte Arthur, Jaremko Łukasz, Testerink Christa, Tester Mark, Julkowska Magdalena M

机构信息

Boyce Thompson Institute, Ithaca, United States.

School of Life Sciences, Lanzhou University, Lanzhou, China.

出版信息

Elife. 2025 Mar 28;13:RP98896. doi: 10.7554/eLife.98896.

DOI:10.7554/eLife.98896
PMID:40153306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11952752/
Abstract

Soil salinity is one of the major threats to agricultural productivity worldwide. Salt stress exposure alters root and shoots growth rates, thereby affecting overall plant performance. While past studies have extensively documented the effect of salt stress on root elongation and shoot development separately, here we take an innovative approach by examining the coordination of root and shoot growth under salt stress conditions. Utilizing a newly developed tool for quantifying the root:shoot ratio in agar-grown seedlings, we found that salt stress results in a loss of coordination between root and shoot growth rates. We identify a specific gene cluster encoding domain-of-unknown-function 247 (DUF247), and characterize one of these genes as alt oot:shoot atio egulator ene (SR3G). Further analysis elucidates the role of SR3G as a negative regulator of salt stress tolerance, revealing its function in regulating shoot growth, root suberization, and sodium accumulation. We further characterize that expression is modulated by transcription factor, known as a positive regulator of salt stress tolerance. Finally, we show that the salt stress sensitivity of mutant is completely diminished when it is combined with mutation. Together, our results demonstrate that utilizing root:shoot ratio as an architectural feature leads to the discovery of a new stress resilience gene. The study's innovative approach and findings not only contribute to our understanding of plant stress tolerance mechanisms but also open new avenues for genetic and agronomic strategies to enhance crop environmental resilience.

摘要

土壤盐渍化是全球农业生产力面临的主要威胁之一。盐胁迫会改变根和地上部的生长速率,从而影响植株整体表现。虽然过去的研究已经广泛记录了盐胁迫对根伸长和地上部发育的单独影响,但在此我们采用一种创新方法,研究盐胁迫条件下根和地上部生长的协调性。利用一种新开发的工具来量化琼脂培养幼苗的根冠比,我们发现盐胁迫导致根和地上部生长速率之间的协调性丧失。我们鉴定出一个编码未知功能结构域247(DUF247)的特定基因簇,并将其中一个基因表征为根冠比调节基因(SR3G)。进一步分析阐明了SR3G作为盐胁迫耐受性负调节因子的作用,揭示了其在调节地上部生长、根木栓化和钠积累方面的功能。我们进一步表征了其表达受一种转录因子调控,该转录因子是盐胁迫耐受性的正调节因子。最后,我们表明,当突变体与另一个突变相结合时,其盐胁迫敏感性完全降低。总之,我们的结果表明,将根冠比作为一种结构特征有助于发现一个新的抗逆基因。该研究的创新方法和发现不仅有助于我们理解植物的胁迫耐受机制,还为增强作物环境适应性的遗传和农艺策略开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/c31d3944c4cd/elife-98896-sa3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/bdb743ef2b58/elife-98896-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8ebdc7658f3a/elife-98896-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/0bf8fb026426/elife-98896-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/0fc365e64b27/elife-98896-fig1-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/61c86dcb636b/elife-98896-fig1-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/bfbe4d4cd969/elife-98896-fig1-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/e5950c0859a5/elife-98896-fig1-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/cead5331d972/elife-98896-fig1-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b9be188d645a/elife-98896-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/19c2d2468f1b/elife-98896-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/431108001ac7/elife-98896-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/90211fd8b1f2/elife-98896-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/264273eb1c37/elife-98896-fig2-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3d8a9776a712/elife-98896-fig2-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b64a5ab988b7/elife-98896-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/2e61fadcc3e3/elife-98896-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8e58e455ff85/elife-98896-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8681fe43759d/elife-98896-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/d926b03fc5f1/elife-98896-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/f15e02bc8cf0/elife-98896-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6c813290b2f3/elife-98896-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/fb3580d59dc2/elife-98896-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/d8631739e87d/elife-98896-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6987042ee7e4/elife-98896-fig6-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b72763baa48e/elife-98896-fig6-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/e2a768be1a4e/elife-98896-fig6-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/c242a9a0664d/elife-98896-fig6-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3407bcf41795/elife-98896-fig6-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/556678416c19/elife-98896-fig6-figsupp8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/ebb69f45d011/elife-98896-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/67e228a8d89c/elife-98896-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/a1f2079845a0/elife-98896-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/186b8f0a9a00/elife-98896-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3fc586faf90f/elife-98896-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/05d04bfa4623/elife-98896-fig10-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6809cf9861ac/elife-98896-fig10-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/c31d3944c4cd/elife-98896-sa3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/bdb743ef2b58/elife-98896-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8ebdc7658f3a/elife-98896-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/0bf8fb026426/elife-98896-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/0fc365e64b27/elife-98896-fig1-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/61c86dcb636b/elife-98896-fig1-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/bfbe4d4cd969/elife-98896-fig1-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/e5950c0859a5/elife-98896-fig1-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/cead5331d972/elife-98896-fig1-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b9be188d645a/elife-98896-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/19c2d2468f1b/elife-98896-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/431108001ac7/elife-98896-fig2-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/90211fd8b1f2/elife-98896-fig2-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/264273eb1c37/elife-98896-fig2-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3d8a9776a712/elife-98896-fig2-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b64a5ab988b7/elife-98896-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/2e61fadcc3e3/elife-98896-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8e58e455ff85/elife-98896-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/8681fe43759d/elife-98896-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/d926b03fc5f1/elife-98896-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/f15e02bc8cf0/elife-98896-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6c813290b2f3/elife-98896-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/fb3580d59dc2/elife-98896-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/d8631739e87d/elife-98896-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6987042ee7e4/elife-98896-fig6-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/b72763baa48e/elife-98896-fig6-figsupp4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/e2a768be1a4e/elife-98896-fig6-figsupp5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/c242a9a0664d/elife-98896-fig6-figsupp6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3407bcf41795/elife-98896-fig6-figsupp7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/556678416c19/elife-98896-fig6-figsupp8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/ebb69f45d011/elife-98896-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/67e228a8d89c/elife-98896-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/a1f2079845a0/elife-98896-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/186b8f0a9a00/elife-98896-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/3fc586faf90f/elife-98896-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/05d04bfa4623/elife-98896-fig10-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/6809cf9861ac/elife-98896-fig10-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a2/11952752/c31d3944c4cd/elife-98896-sa3-fig1.jpg

相似文献

1
Natural variation in salt-induced changes in root:shoot ratio reveals SR3G as a negative regulator of root suberization and salt resilience in .盐诱导的根冠比变化中的自然变异揭示了SR3G作为拟南芥根木栓化和耐盐性的负调控因子。 (注:原文中“in.”应该是不完整信息,推测补充为“in Arabidopsis thaliana”进行了完整翻译,具体需结合完整原文判断 )
Elife. 2025 Mar 28;13:RP98896. doi: 10.7554/eLife.98896.
2
Trichoderma spp. Improve growth of Arabidopsis seedlings under salt stress through enhanced root development, osmolite production, and Na⁺ elimination through root exudates.木霉属通过增强根发育、渗透调节剂的产生以及通过根分泌物排出钠离子来改善盐胁迫下拟南芥幼苗的生长。
Mol Plant Microbe Interact. 2014 Jun;27(6):503-14. doi: 10.1094/MPMI-09-13-0265-R.
3
Phylogenetically diverse endophytic bacteria from desert plants induce transcriptional changes of tissue-specific ion transporters and salinity stress in Arabidopsis thaliana.来自沙漠植物的具有系统发育多样性的内生细菌诱导拟南芥组织特异性离子转运体和盐胁迫的转录变化。
Plant Sci. 2019 Mar;280:228-240. doi: 10.1016/j.plantsci.2018.12.002. Epub 2018 Dec 7.
4
Overexpression of PP2A-C5 that encodes the catalytic subunit 5 of protein phosphatase 2A in Arabidopsis confers better root and shoot development under salt conditions.在拟南芥中,编码蛋白磷酸酶2A催化亚基5的PP2A-C5的过表达赋予了在盐胁迫条件下更好的根和地上部发育。
Plant Cell Environ. 2017 Jan;40(1):150-164. doi: 10.1111/pce.12837. Epub 2016 Oct 26.
5
Allantoin accumulation mediated by allantoinase downregulation and transport by Ureide Permease 5 confers salt stress tolerance to Arabidopsis plants.尿囊素酶下调介导的尿囊素积累和尿囊素透性酶 5 的运输使拟南芥植物具有耐盐胁迫能力。
Plant Mol Biol. 2016 Jul;91(4-5):581-95. doi: 10.1007/s11103-016-0490-7. Epub 2016 May 21.
6
Analysis of Arabidopsis thaliana HKT1 and Eutrema salsugineum/botschantzevii HKT1;2 Promoters in Response to Salt Stress in Athkt1:1 Mutant.拟南芥 HKT1 和盐地碱蓬/滨藜 HKT1;2 启动子在 Athkt1:1 突变体响应盐胁迫中的分析。
Mol Biotechnol. 2019 Jun;61(6):442-450. doi: 10.1007/s12033-019-00175-5.
7
Phosphorylated B6 vitamer deficiency in SALT OVERLY SENSITIVE 4 mutants compromises shoot and root development.SALT OVERLY SENSITIVE 4 突变体中磷酸化 B6 维生素缺乏会影响 shoot 和 root 的发育。
Plant Physiol. 2022 Jan 20;188(1):220-240. doi: 10.1093/plphys/kiab475.
8
dhm1, an Arabidopsis mutant with increased sensitivity to alkamides shows tumorous shoot development and enhanced lateral root formation.dhm1 是拟南芥突变体,对酰胺类化合物的敏感性增加,表现出肿瘤状的芽发育和增强的侧根形成。
Plant Mol Biol. 2013 Apr;81(6):609-25. doi: 10.1007/s11103-013-0023-6. Epub 2013 Feb 15.
9
Capturing Arabidopsis root architecture dynamics with ROOT-FIT reveals diversity in responses to salinity.利用ROOT-FIT捕捉拟南芥根系结构动态揭示了对盐度反应的多样性。
Plant Physiol. 2014 Nov;166(3):1387-402. doi: 10.1104/pp.114.248963. Epub 2014 Sep 30.
10
Genetic Components of Root Architecture Remodeling in Response to Salt Stress.盐胁迫下根系架构重塑的遗传组成。
Plant Cell. 2017 Dec;29(12):3198-3213. doi: 10.1105/tpc.16.00680. Epub 2017 Nov 7.

引用本文的文献

1
The Physiological Mechanisms and Hurdles of Efficient Water-Nitrogen Utilization in Maize Production: A Review.玉米生产中高效水分-氮素利用的生理机制与障碍:综述
Plants (Basel). 2025 Jun 20;14(13):1899. doi: 10.3390/plants14131899.

本文引用的文献

1
Development of a mobile, high-throughput, and low-cost image-based plant growth phenotyping system.一种基于图像的移动、高通量且低成本的植物生长表型分析系统的开发。
Plant Physiol. 2024 Oct 1;196(2):810-829. doi: 10.1093/plphys/kiae237.
2
Arabinosylation of cell wall extensin is required for the directional response to salinity in roots.细胞壁伸展蛋白的阿拉伯糖基化是根系对盐度定向响应所必需的。
Plant Cell. 2024 Sep 3;36(9):3328-3343. doi: 10.1093/plcell/koae135.
3
NIGT1.4 maintains primary root elongation in response to salt stress through induction of ERF1 in Arabidopsis.
NIGT1.4 通过诱导拟南芥中的 ERF1 来维持主根伸长以响应盐胁迫。
Plant J. 2023 Oct;116(1):173-186. doi: 10.1111/tpj.16369. Epub 2023 Jul 5.
4
A stratagem for primary root elongation under moderate salt stress in the halophyte Schrenkiella parvula.盐沼植物星星草在中等盐胁迫下促进主根伸长的策略。
Physiol Plant. 2023 May-Jun;175(3):e13937. doi: 10.1111/ppl.13937.
5
CycC1;1-WRKY75 complex-mediated transcriptional regulation of SOS1 controls salt stress tolerance in Arabidopsis.CycC1;1-WRKY75 复合物介导的 SOS1 转录调控控制拟南芥的耐盐性。
Plant Cell. 2023 Jun 26;35(7):2570-2591. doi: 10.1093/plcell/koad105.
6
Root twisting drives halotropism via stress-induced microtubule reorientation.根扭转通过胁迫诱导的微管重排驱动向地性。
Dev Cell. 2022 Oct 24;57(20):2412-2425.e6. doi: 10.1016/j.devcel.2022.09.012. Epub 2022 Oct 14.
7
Phosphorylation of SWEET sucrose transporters regulates plant root:shoot ratio under drought.磷酸化 SWEET 蔗糖转运蛋白调控植物根系/地上部比值对干旱的响应。
Nat Plants. 2022 Jan;8(1):68-77. doi: 10.1038/s41477-021-01040-7. Epub 2021 Dec 23.
8
Global predictions of primary soil salinization under changing climate in the 21st century.21 世纪气候变化下主要土壤盐渍化的全球预测。
Nat Commun. 2021 Nov 18;12(1):6663. doi: 10.1038/s41467-021-26907-3.
9
Modifying root-to-shoot ratio improves root water influxes in wheat under drought stress.改变根冠比可提高干旱胁迫下小麦的根水吸收。
J Exp Bot. 2022 Mar 2;73(5):1643-1654. doi: 10.1093/jxb/erab500.
10
Suberin plasticity to developmental and exogenous cues is regulated by a set of MYB transcription factors.蜡质可塑性受一组 MYB 转录因子调控,这些因子对发育和外源信号做出响应。
Proc Natl Acad Sci U S A. 2021 Sep 28;118(39). doi: 10.1073/pnas.2101730118.