• 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

拟南芥隐花色素 2 在蓝光下与 TCP22 形成光体,并调节生物钟。

Arabidopsis cryptochrome 2 forms photobodies with TCP22 under blue light and regulates the circadian clock.

机构信息

Jilin Province Engineering Laboratory of Plant Genetic Improvement, College of Plant Science, Jilin University, 5333 Xi'an Road, Changchun, 130062, China.

Basic Forestry and Proteomics Research Center, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.

出版信息

Nat Commun. 2022 May 12;13(1):2631. doi: 10.1038/s41467-022-30231-9.

DOI:10.1038/s41467-022-30231-9
PMID:35551190
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9098493/
Abstract

Cryptochromes are blue light receptors that regulate plant growth and development. They also act as the core components of the central clock oscillator in animals. Although plant cryptochromes have been reported to regulate the circadian clock in blue light, how they do so is unclear. Here we show that Arabidopsis cryptochrome 2 (CRY2) forms photobodies with the TCP22 transcription factor in response to blue light in plant cells. We provide evidence that PPK kinases influence the characteristics of these photobodies and that together these components, along with LWD transcriptional regulators, can positively regulate the expression of CCA1 encoding a central component of the circadian oscillator.

摘要

隐花色素是蓝光受体,调节植物的生长和发育。它们也是动物中央时钟振荡器的核心组成部分。虽然已经报道植物隐花色素在蓝光下调节生物钟,但具体机制尚不清楚。本研究表明,拟南芥隐花色素 2(CRY2)在植物细胞中对蓝光作出反应时与 TCP22 转录因子形成光体。本研究提供了证据表明 PPK 激酶影响这些光体的特性,并且这些成分与 LWD 转录调节剂一起,可以正向调节编码生物钟中央振荡器的核心成分 CCA1 的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/aeb39da10fbf/41467_2022_30231_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/5217cbdf7cd8/41467_2022_30231_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/a105923252ed/41467_2022_30231_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/166ea56dde6b/41467_2022_30231_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/bd636c6f3582/41467_2022_30231_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/216d9c71a274/41467_2022_30231_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/aeb39da10fbf/41467_2022_30231_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/5217cbdf7cd8/41467_2022_30231_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/a105923252ed/41467_2022_30231_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/166ea56dde6b/41467_2022_30231_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/bd636c6f3582/41467_2022_30231_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/216d9c71a274/41467_2022_30231_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/9098493/aeb39da10fbf/41467_2022_30231_Fig6_HTML.jpg

相似文献

1
Arabidopsis cryptochrome 2 forms photobodies with TCP22 under blue light and regulates the circadian clock.拟南芥隐花色素 2 在蓝光下与 TCP22 形成光体,并调节生物钟。
Nat Commun. 2022 May 12;13(1):2631. doi: 10.1038/s41467-022-30231-9.
2
Protoplast System for Studying Blue-Light-Dependent Formation of Cryptochrome Photobody.原核生物系统用于研究蓝光依赖性隐花色素光体的形成。
Methods Mol Biol. 2021;2297:105-113. doi: 10.1007/978-1-0716-1370-2_11.
3
Aschoff's rule on circadian rhythms orchestrated by blue light sensor CRY2 and clock component PRR9.生物钟节律的阿肖夫法则由蓝光感受器 CRY2 和时钟组件 PRR9 协调。
Nat Commun. 2022 Oct 5;13(1):5869. doi: 10.1038/s41467-022-33568-3.
4
Universal Stress Protein regulates the circadian rhythm of central oscillator genes in Arabidopsis.泛素应激蛋白调控拟南芥生物钟核心基因的节律。
FEBS Lett. 2022 Aug;596(15):1871-1880. doi: 10.1002/1873-3468.14410. Epub 2022 Jun 16.
5
Proteasomal regulation of CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) stability is part of the complex control of CCA1.蛋白酶体对 CIRCADIAN CLOCK ASSOCIATED 1(CCA1)稳定性的调节是 CCA1 复杂调控的一部分。
Plant Signal Behav. 2013 Mar;8(3):e23206. doi: 10.4161/psb.23206. Epub 2013 Jan 8.
6
CIRCADIAN CLOCK ASSOCIATED1 transcript stability and the entrainment of the circadian clock in Arabidopsis.拟南芥中生物钟关联基因 1 的转录本稳定性与生物钟的同步调节
Plant Physiol. 2007 Nov;145(3):925-32. doi: 10.1104/pp.107.103812. Epub 2007 Sep 14.
7
Network balance via CRY signalling controls the Arabidopsis circadian clock over ambient temperatures.通过 CRY 信号实现的网络平衡控制着拟南芥生物钟对环境温度的反应。
Mol Syst Biol. 2013;9:650. doi: 10.1038/msb.2013.7.
8
The dual-action mechanism of Arabidopsis cryptochromes.拟南芥隐花色素的双重作用机制。
J Integr Plant Biol. 2024 May;66(5):883-896. doi: 10.1111/jipb.13578. Epub 2024 Jan 2.
9
Double loss-of-function mutation in EARLY FLOWERING 3 and CRYPTOCHROME 2 genes delays flowering under continuous light but accelerates it under long days and short days: an important role for Arabidopsis CRY2 to accelerate flowering time in continuous light.EARLY FLOWERING 3 和 CRYPTOCHROME 2 基因的双功能丧失突变会延迟连续光照下的开花,但会加速长日照和短日照下的开花:拟南芥 CRY2 对在连续光照下加速开花时间的重要作用。
J Exp Bot. 2011 May;62(8):2731-44. doi: 10.1093/jxb/erq450. Epub 2011 Feb 4.
10
A CRY-BIC negative-feedback circuitry regulating blue light sensitivity of Arabidopsis.调控拟南芥蓝光敏感性的 CRY-BIC 负反馈电路。
Plant J. 2017 Nov;92(3):426-436. doi: 10.1111/tpj.13664. Epub 2017 Oct 9.

引用本文的文献

1
Transcriptional activation and repression in the plant circadian clock: Revisiting core oscillator feedback loops and output pathways.植物生物钟中的转录激活与抑制:重新审视核心振荡器反馈环及输出途径
Plant Commun. 2025 Aug 11;6(8):101415. doi: 10.1016/j.xplc.2025.101415. Epub 2025 Jun 10.
2
AlphaFold-Guided Bespoke Gene Editing Enhances Field-Grown Soybean Oil Contents.基于AlphaFold的定制基因编辑提高田间种植大豆的油含量。
Adv Sci (Weinh). 2025 Jun;12(23):e2500290. doi: 10.1002/advs.202500290. Epub 2025 May 14.
3
Hierarchical Regulatory Networks Reveal Conserved Drivers of Plant Drought Response at the Cell-Type Level.

本文引用的文献

1
The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences.PRIDE 数据库资源在 2022 年:一个基于质谱的蛋白质组学证据的中心。
Nucleic Acids Res. 2022 Jan 7;50(D1):D543-D552. doi: 10.1093/nar/gkab1038.
2
Co-condensation between transcription factor and coactivator p300 modulates transcriptional bursting kinetics.转录因子和共激活因子 p300 的共凝聚调节转录爆发动力学。
Mol Cell. 2021 Apr 15;81(8):1682-1697.e7. doi: 10.1016/j.molcel.2021.01.031. Epub 2021 Mar 1.
3
An intrinsically disordered region-mediated confinement state contributes to the dynamics and function of transcription factors.
层次化调控网络揭示了细胞类型水平上植物干旱响应的保守驱动因素。
Adv Sci (Weinh). 2025 May;12(18):e2415106. doi: 10.1002/advs.202415106. Epub 2025 Mar 16.
4
The dark activity of Arabidopsis blue-light receptor CRY2.拟南芥蓝光受体CRY2的暗活性
Sci China Life Sci. 2025 Mar;68(3):887-889. doi: 10.1007/s11427-024-2788-y. Epub 2024 Nov 29.
5
Transcription regulation by biomolecular condensates.生物分子凝聚物介导的转录调控
Nat Rev Mol Cell Biol. 2025 Mar;26(3):213-236. doi: 10.1038/s41580-024-00789-x. Epub 2024 Nov 8.
6
Basic design of artificial membrane-less organelles using condensation-prone proteins in plant cells.利用植物细胞中易凝聚的蛋白质设计人工无膜细胞器。
Commun Biol. 2024 Oct 26;7(1):1396. doi: 10.1038/s42003-024-07102-8.
7
Diel transcriptional responses of coral-Symbiodiniaceae holobiont to elevated temperature.昼夜转录对珊瑚-共生藻共生体对高温的响应。
Commun Biol. 2024 Jul 19;7(1):882. doi: 10.1038/s42003-024-06542-6.
8
Phase separation: a new window in RALF signaling.相分离:RALF信号传导的新窗口
Front Plant Sci. 2024 Jun 27;15:1409770. doi: 10.3389/fpls.2024.1409770. eCollection 2024.
9
Twilight length alters growth and flowering time in Arabidopsis via /.暮光长度通过 /. 改变拟南芥的生长和开花时间。
Sci Adv. 2024 Jun 28;10(26):eadl3199. doi: 10.1126/sciadv.adl3199.
10
Arabidopsis CaLB1 undergoes phase separation with the ESCRT protein ALIX and modulates autophagosome maturation.拟南芥 CaLB1 与 ESCRT 蛋白 ALIX 发生液-液相分离,调节自噬体成熟。
Nat Commun. 2024 Jun 19;15(1):5188. doi: 10.1038/s41467-024-49485-6.
一个固有无序区域介导的约束状态有助于转录因子的动力学和功能。
Mol Cell. 2021 Apr 1;81(7):1484-1498.e6. doi: 10.1016/j.molcel.2021.01.013. Epub 2021 Feb 8.
4
Liquid-liquid phase separation of light-inducible transcription factors increases transcription activation in mammalian cells and mice.光诱导转录因子的液-液相分离增加了哺乳动物细胞和小鼠中的转录激活。
Sci Adv. 2021 Jan 1;7(1). doi: 10.1126/sciadv.abd3568. Print 2021 Jan.
5
Mechanisms of Cryptochrome-Mediated Photoresponses in Plants.植物中隐花色素介导的光响应机制。
Annu Rev Plant Biol. 2020 Apr 29;71:103-129. doi: 10.1146/annurev-arplant-050718-100300. Epub 2020 Mar 13.
6
Transcription Factors FHY3 and FAR1 Regulate Light-Induced Gene Expression in Arabidopsis.转录因子 FHY3 和 FAR1 调控拟南芥光诱导基因表达。
Plant Cell. 2020 May;32(5):1464-1478. doi: 10.1105/tpc.19.00981. Epub 2020 Mar 9.
7
Light Perception: A Matter of Time.光感知:时间的问题。
Mol Plant. 2020 Mar 2;13(3):363-385. doi: 10.1016/j.molp.2020.02.006. Epub 2020 Feb 14.
8
Molecular mechanisms and physiological importance of circadian rhythms.昼夜节律的分子机制和生理重要性。
Nat Rev Mol Cell Biol. 2020 Feb;21(2):67-84. doi: 10.1038/s41580-019-0179-2. Epub 2019 Nov 25.
9
TTG1 proteins regulate circadian activity as well as epidermal cell fate and pigmentation.TTG1 蛋白调节昼夜节律活动以及表皮细胞命运和色素沉着。
Nat Plants. 2019 Nov;5(11):1145-1153. doi: 10.1038/s41477-019-0544-3. Epub 2019 Nov 11.
10
Pol II phosphorylation regulates a switch between transcriptional and splicing condensates.Pol II 磷酸化调节转录和剪接凝聚物之间的转换。
Nature. 2019 Aug;572(7770):543-548. doi: 10.1038/s41586-019-1464-0. Epub 2019 Aug 7.