• 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

生长素信息的时间整合在模式形成中的调节作用。

Temporal integration of auxin information for the regulation of patterning.

机构信息

Laboratoire Reproduction et Développement des Plantes, Univ Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, Inria, Lyon, France.

Department of Stem Cell Biology, Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.

出版信息

Elife. 2020 May 7;9:e55832. doi: 10.7554/eLife.55832.

DOI:10.7554/eLife.55832
PMID:32379043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7205470/
Abstract

Positional information is essential for coordinating the development of multicellular organisms. In plants, positional information provided by the hormone auxin regulates rhythmic organ production at the shoot apex, but the spatio-temporal dynamics of auxin gradients is unknown. We used quantitative imaging to demonstrate that auxin carries high-definition graded information not only in space but also in time. We show that, during organogenesis, temporal patterns of auxin arise from rhythmic centrifugal waves of high auxin travelling through the tissue faster than growth. We further demonstrate that temporal integration of auxin concentration is required to trigger the auxin-dependent transcription associated with organogenesis. This provides a mechanism to temporally differentiate sites of organ initiation and exemplifies how spatio-temporal positional information can be used to create rhythmicity.

摘要

位置信息对于协调多细胞生物的发育至关重要。在植物中,激素生长素提供的位置信息调节着茎尖有节奏的器官产生,但生长素梯度的时空动态尚不清楚。我们使用定量成像技术证明,生长素不仅在空间上,而且在时间上传递高清晰度的分级信息。我们表明,在器官发生过程中,生长素的时间模式源于通过组织快速移动的高生长素的有节奏的离心波,其速度快于生长。我们进一步证明,生长素浓度的时间整合对于触发与器官发生相关的生长素依赖性转录是必需的。这为时间上区分器官起始点提供了一种机制,并例证了时空位置信息如何用于产生节律性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/32e328eca35f/elife-55832-app5-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/1f1bb301fd84/elife-55832-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/25edbfc2a5c4/elife-55832-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/7ba22fde0a5d/elife-55832-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/f11327908c3b/elife-55832-fig1-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/137b44d1b9c3/elife-55832-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/f7cf8ec67b77/elife-55832-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/646b1224a849/elife-55832-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/84d74c5aa04f/elife-55832-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/1370d8b2478a/elife-55832-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/c22574bf1c83/elife-55832-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/89d2d5d9ebb9/elife-55832-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/ac7e5db13f8a/elife-55832-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/76860525efe5/elife-55832-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/e525c8a404f0/elife-55832-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/fca6a4505e9c/elife-55832-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/6549b89bf6a4/elife-55832-app2-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/b70b386d8f55/elife-55832-app3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/619ea4366219/elife-55832-app3-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/8af865b66108/elife-55832-app3-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/e6c729dfa118/elife-55832-app3-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/d8748070a977/elife-55832-app4-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/490381a40778/elife-55832-app4-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/ad70d43cc7f9/elife-55832-app4-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/32e328eca35f/elife-55832-app5-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/1f1bb301fd84/elife-55832-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/25edbfc2a5c4/elife-55832-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/7ba22fde0a5d/elife-55832-fig1-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/f11327908c3b/elife-55832-fig1-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/137b44d1b9c3/elife-55832-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/f7cf8ec67b77/elife-55832-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/646b1224a849/elife-55832-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/84d74c5aa04f/elife-55832-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/1370d8b2478a/elife-55832-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/c22574bf1c83/elife-55832-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/89d2d5d9ebb9/elife-55832-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/ac7e5db13f8a/elife-55832-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/76860525efe5/elife-55832-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/e525c8a404f0/elife-55832-fig5-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/fca6a4505e9c/elife-55832-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/6549b89bf6a4/elife-55832-app2-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/b70b386d8f55/elife-55832-app3-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/619ea4366219/elife-55832-app3-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/8af865b66108/elife-55832-app3-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/e6c729dfa118/elife-55832-app3-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/d8748070a977/elife-55832-app4-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/490381a40778/elife-55832-app4-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/ad70d43cc7f9/elife-55832-app4-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f833/7205470/32e328eca35f/elife-55832-app5-fig1.jpg

相似文献

1
Temporal integration of auxin information for the regulation of patterning.生长素信息的时间整合在模式形成中的调节作用。
Elife. 2020 May 7;9:e55832. doi: 10.7554/eLife.55832.
2
Connective auxin transport contributes to strigolactone-mediated shoot branching control independent of the transcription factor BRC1.连接生长素运输有助于独于转录因子 BRC1 介导的赤霉素介导的分枝控制。
PLoS Genet. 2019 Mar 13;15(3):e1008023. doi: 10.1371/journal.pgen.1008023. eCollection 2019 Mar.
3
The auxin signalling network translates dynamic input into robust patterning at the shoot apex.生长素信号网络将动态输入转化为茎尖的稳健模式。
Mol Syst Biol. 2011 Jul 5;7:508. doi: 10.1038/msb.2011.39.
4
The Arabidopsis transcription factor AINTEGUMENTA orchestrates patterning genes and auxin signaling in the establishment of floral growth and form.拟南芥转录因子 AINTEGUMENTA 在花的生长和形态建立过程中协调模式基因和生长素信号。
Plant J. 2020 Jul;103(2):752-768. doi: 10.1111/tpj.14769. Epub 2020 May 5.
5
A Molecular Framework for Auxin-Controlled Homeostasis of Shoot Stem Cells in Arabidopsis.生长素控制拟南芥茎干细胞稳态的分子框架。
Mol Plant. 2018 Jul 2;11(7):899-913. doi: 10.1016/j.molp.2018.04.006. Epub 2018 May 3.
6
Auxin and self-organization at the shoot apical meristem.生长素与茎尖分生组织的自组织。
J Exp Bot. 2013 Jun;64(9):2579-92. doi: 10.1093/jxb/ert101. Epub 2013 Apr 12.
7
MAB4-induced auxin sink generates local auxin gradients in Arabidopsis organ formation.MAB4 诱导的生长素汇在拟南芥器官形成中产生局部生长素梯度。
Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):1198-203. doi: 10.1073/pnas.1316109111. Epub 2014 Jan 6.
8
Patterns of auxin transport and gene expression during primordium development revealed by live imaging of the Arabidopsis inflorescence meristem.通过拟南芥花序分生组织的实时成像揭示原基发育过程中生长素运输和基因表达的模式。
Curr Biol. 2005 Nov 8;15(21):1899-911. doi: 10.1016/j.cub.2005.09.052.
9
ERECTA family genes regulate auxin transport in the shoot apical meristem and forming leaf primordia.ERECTA 家族基因调节茎尖分生组织中的生长素运输和形成叶原基。
Plant Physiol. 2013 Aug;162(4):1978-91. doi: 10.1104/pp.113.218198. Epub 2013 Jul 2.
10
Simulation of organ patterning on the floral meristem using a polar auxin transport model.利用极性生长素运输模型模拟花分生组织中的器官模式形成。
PLoS One. 2012;7(1):e28762. doi: 10.1371/journal.pone.0028762. Epub 2012 Jan 23.

引用本文的文献

1
Best practices in plant fluorescence imaging and reporting: A primer.植物荧光成像与报告的最佳实践:入门指南。
Plant Cell. 2025 Jul 1;37(7). doi: 10.1093/plcell/koaf143.
2
Canalization of flower production across thermal environments requires Florigen and CLAVATA signaling.跨热环境的成花过程的 canalization 需要成花素和 CLAVATA 信号传导。 (注:这里的“canalization”可能在特定医学或生物学语境中有更准确的专业释义,若有需要可进一步结合专业知识完善表述。)
Curr Biol. 2025 Jun 25. doi: 10.1016/j.cub.2025.06.001.
3
Transcriptional Tuning: How Auxin Strikes Unique Chords in Gene Regulation.

本文引用的文献

1
SciPy 1.0: fundamental algorithms for scientific computing in Python.SciPy 1.0:Python 中的科学计算基础算法。
Nat Methods. 2020 Mar;17(3):261-272. doi: 10.1038/s41592-019-0686-2. Epub 2020 Feb 3.
2
WUSCHEL acts as an auxin response rheostat to maintain apical stem cells in Arabidopsis.WUSCHEL 作为生长素反应变阻器,维持拟南芥顶端干细胞。
Nat Commun. 2019 Nov 8;10(1):5093. doi: 10.1038/s41467-019-13074-9.
3
PIN-FORMED and PIN-LIKES auxin transport facilitators.PIN 形成蛋白和 PIN 样生长素运输促进因子。
转录调控:生长素如何在基因调控中奏响独特乐章
Physiol Plant. 2025 May-Jun;177(3):e70229. doi: 10.1111/ppl.70229.
4
Canalization of flower production across thermal environments requires Florigen and CLAVATA signaling.花的产生在不同热环境下的信号传导需要成花素和CLAVATA信号通路。
bioRxiv. 2025 Mar 25:2025.03.23.644808. doi: 10.1101/2025.03.23.644808.
5
Modeling Arabidopsis root growth and development.拟南芥根生长与发育的建模
Plant Physiol. 2025 Feb 7;197(2). doi: 10.1093/plphys/kiaf045.
6
Behind phyllotaxis, within the meristem: a REM-ARF complex shapes inflorescence in Arabidopsis thaliana.在拟南芥叶序背后,分生组织内部:一个REM-ARF复合体塑造花序。
Plant J. 2025 Mar;121(5):e70041. doi: 10.1111/tpj.70041.
7
Evolution of a SHOOTMERISTEMLESS transcription factor binding site promotes fruit shape determination.无茎分生组织转录因子结合位点的进化促进果实形状的决定。
Nat Plants. 2025 Jan;11(1):23-35. doi: 10.1038/s41477-024-01854-1. Epub 2024 Dec 12.
8
Identification of potential auxin response candidate genes for soybean rapid canopy coverage through comparative evolution and expression analysis.通过比较进化和表达分析鉴定大豆快速覆盖冠层的潜在生长素反应候选基因。
Front Plant Sci. 2024 Oct 3;15:1463438. doi: 10.3389/fpls.2024.1463438. eCollection 2024.
9
Genetically Encoded, Noise-Tolerant, Auxin Biosensors in Yeast.酵母中基因编码、抗噪声、生长素生物传感器。
ACS Synth Biol. 2024 Sep 20;13(9):2804-2819. doi: 10.1021/acssynbio.4c00186. Epub 2024 Aug 28.
10
A quantitative gibberellin signaling biosensor reveals a role for gibberellins in internode specification at the shoot apical meristem.一种定量赤霉素信号生物传感器揭示了赤霉素在芽顶端分生组织中节间特化中的作用。
Nat Commun. 2024 May 8;15(1):3895. doi: 10.1038/s41467-024-48116-4.
Development. 2019 Aug 1;146(15):dev168088. doi: 10.1242/dev.168088.
4
Auxin Response Factors promote organogenesis by chromatin-mediated repression of the pluripotency gene SHOOTMERISTEMLESS.生长素响应因子通过染色质介导抑制多能性基因 SHOOT 分生组织起始来促进器官发生。
Nat Commun. 2019 Feb 21;10(1):886. doi: 10.1038/s41467-019-08861-3.
5
Transcriptional induction of cell wall remodelling genes is coupled to microtubule-driven growth isotropy at the shoot apex in .细胞壁重塑基因的转录诱导与顶端分生组织中微管驱动的生长各向同性相关。
Development. 2018 Jun 4;145(11):dev162255. doi: 10.1242/dev.162255.
6
Feedback from Lateral Organs Controls Shoot Apical Meristem Growth by Modulating Auxin Transport.侧向器官的反馈通过调节生长素运输来控制茎尖分生组织的生长。
Dev Cell. 2018 Jan 22;44(2):204-216.e6. doi: 10.1016/j.devcel.2017.12.021.
7
Systematic characterization of maturation time of fluorescent proteins in living cells.活细胞中荧光蛋白成熟时间的系统表征。
Nat Methods. 2018 Jan;15(1):47-51. doi: 10.1038/nmeth.4509. Epub 2017 Nov 20.
8
Cell type boundaries organize plant development.细胞类型边界组织植物发育。
Elife. 2017 Sep 12;6:e27421. doi: 10.7554/eLife.27421.
9
Model for the role of auxin polar transport in patterning of the leaf adaxial-abaxial axis.生长素极性运输在叶片腹背轴模式形成中的作用模型。
Plant J. 2017 Nov;92(3):469-480. doi: 10.1111/tpj.13670. Epub 2017 Sep 26.
10
Auxin-Induced Modulation of ETTIN Activity Orchestrates Gene Expression in Arabidopsis.生长素诱导的 ETTIN 活性调控调控拟南芥基因表达。
Plant Cell. 2017 Aug;29(8):1864-1882. doi: 10.1105/tpc.17.00389. Epub 2017 Aug 13.