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脱落酸介导的光敏色素B信号传导促进拟南芥主根生长。

Abscisic acid-mediated phytochrome B signaling promotes primary root growth in Arabidopsis.

作者信息

Gil K-E, Ha J-H, Park C-M

机构信息

a Department of Chemistry , Seoul National University , Seoul , Korea.

b Plant Genomics and Breeding Institute , Seoul National University , Seoul , Korea.

出版信息

Plant Signal Behav. 2018;13(5):e1473684. doi: 10.1080/15592324.2018.1473684. Epub 2018 Jun 25.

DOI:10.1080/15592324.2018.1473684
PMID:29939823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6103287/
Abstract

Plant photomorphogenic responses have been studied mostly using the shoots, the core part of plant architecture that perceives light for photosynthesis and influences the overall processes of growth and development. While the roots are also known to respond to aboveground light through multiple routes of light signal transduction, root photomorphogenesis has been less highlighted until recently. A long-standing, critical question was how the underground roots are capable of sensing aerial light and how the root-sensed light signals trigger root photomorphogenesis. When the roots are directly exposed to light, reactive oxygen species (ROS) are rapidly produced to promote primary root elongation, which helps the roots to escape from the abnormal growth conditions. However, severe or long-term exposure of the roots to light causes ROS burst, which impose oxidative damages, leading to a reduction of root growth. We have recently found that phytochrome B (phyB) promotes abscisic acid (ABA) biosynthesis in the shoots and the shoot-derived ABA signals mediate ROS detoxification in the roots, lessening the detrimental effects of light on root growth. On the basis of these observations we propose that the phyB-mediated ABA signaling contributes to the shoot-root synchronization that is essential for optimal growth and performance in plants.

摘要

植物的光形态建成反应大多是利用地上部分进行研究的,地上部分是植物结构的核心部分,负责感知光照以进行光合作用,并影响生长和发育的整体过程。虽然已知根系也能通过多种光信号转导途径对地上光照做出反应,但直到最近,根系光形态建成才受到较少关注。一个长期存在的关键问题是,地下根系如何能够感知地上光照,以及根系感知到的光信号如何触发根系光形态建成。当根系直接暴露在光照下时,会迅速产生活性氧(ROS)以促进主根伸长,这有助于根系摆脱异常生长条件。然而,根系长时间或严重暴露在光照下会导致ROS爆发,造成氧化损伤,从而导致根系生长减缓。我们最近发现,光敏色素B(phyB)促进地上部分脱落酸(ABA)的生物合成,而地上部分产生的ABA信号介导根系中的ROS解毒,减轻光照对根系生长的不利影响。基于这些观察结果,我们提出phyB介导的ABA信号传导有助于地上-地下同步,这对植物的最佳生长和性能至关重要。

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本文引用的文献

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Shoot phytochrome B modulates reactive oxygen species homeostasis in roots via abscisic acid signaling in Arabidopsis.光敏色素 B 通过拟南芥中的脱落酸信号调控根系中的活性氧稳态。
Plant J. 2018 Jun;94(5):790-798. doi: 10.1111/tpj.13902. Epub 2018 Apr 17.
2
Underground roots monitor aboveground environment by sensing stem-piped light.地下根系通过感知茎干输送的光线来监测地上环境。
Commun Integr Biol. 2016 Dec 9;9(6):e1261769. doi: 10.1080/19420889.2016.1261769. eCollection 2016.
3
Stem-piped light activates phytochrome B to trigger light responses in Arabidopsis thaliana roots.茎导管光激活光敏色素B以触发拟南芥根中的光反应。
Sci Signal. 2016 Nov 1;9(452):ra106. doi: 10.1126/scisignal.aaf6530.
4
UV-B Induced Generation of Reactive Oxygen Species Promotes Formation of BFA-Induced Compartments in Cells of Arabidopsis Root Apices.UV-B诱导的活性氧生成促进拟南芥根尖细胞中BFA诱导区室的形成。
Front Plant Sci. 2016 Jan 13;6:1162. doi: 10.3389/fpls.2015.01162. eCollection 2015.
5
Light as stress factor to plant roots - case of root halotropism.光作为植物根系的胁迫因子——以根向性为例。
Front Plant Sci. 2014 Dec 12;5:718. doi: 10.3389/fpls.2014.00718. eCollection 2014.
6
Involvement of plant endogenous ABA in Bacillus megaterium PGPR activity in tomato plants.植物内源 ABA 参与巨大芽孢杆菌 PGPR 在番茄植株中的活性。
BMC Plant Biol. 2014 Jan 25;14:36. doi: 10.1186/1471-2229-14-36.
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SCAR mediates light-induced root elongation in Arabidopsis through photoreceptors and proteasomes.SCAR 通过光受体和蛋白酶体介导拟南芥光诱导的根伸长。
Plant Cell. 2011 Oct;23(10):3610-26. doi: 10.1105/tpc.111.088823. Epub 2011 Oct 4.
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Lotus japonicus nodulation is photomorphogenetically controlled by sensing the red/far red (R/FR) ratio through jasmonic acid (JA) signaling.豌豆结瘤是通过茉莉酸(JA)信号感知红光/远红光(R/FR)比值来光形态建成控制的。
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Transcriptional regulation of ROS controls transition from proliferation to differentiation in the root.ROS 的转录调控控制根中从增殖到分化的转变。
Cell. 2010 Nov 12;143(4):606-16. doi: 10.1016/j.cell.2010.10.020.
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