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本文引用的文献

1
Plant Physiology: Redefining the Enigma of Metabolism in Stomatal Movement.植物生理学:重新定义气孔运动中代谢的奥秘。
Curr Biol. 2016 Feb 8;26(3):R107-9. doi: 10.1016/j.cub.2015.12.025.
2
β-amylase 1 (BAM1) degrades transitory starch to sustain proline biosynthesis during drought stress.β-淀粉酶1(BAM1)降解暂态淀粉以在干旱胁迫期间维持脯氨酸生物合成。
J Exp Bot. 2016 Mar;67(6):1819-26. doi: 10.1093/jxb/erv572. Epub 2016 Jan 20.
3
Blue Light Induces a Distinct Starch Degradation Pathway in Guard Cells for Stomatal Opening.蓝光在保卫细胞中诱导了一个独特的淀粉降解途径以开启气孔。
Curr Biol. 2016 Feb 8;26(3):362-70. doi: 10.1016/j.cub.2015.12.036. Epub 2016 Jan 7.
4
New insights into redox control of starch degradation.淀粉降解氧化还原调控的新见解
Curr Opin Plant Biol. 2015 Jun;25:1-9. doi: 10.1016/j.pbi.2015.04.003. Epub 2015 Apr 19.
5
How plants manage food reserves at night: quantitative models and open questions.植物如何在夜间管理食物储备:定量模型与未解决的问题。
Front Plant Sci. 2015 Mar 31;6:204. doi: 10.3389/fpls.2015.00204. eCollection 2015.
6
Carbon partitioning in Arabidopsis thaliana is a dynamic process controlled by the plants metabolic status and its circadian clock.拟南芥中的碳分配是一个由植物代谢状态及其生物钟控制的动态过程。
Plant Cell Environ. 2015 Oct;38(10):1965-79. doi: 10.1111/pce.12512. Epub 2015 Apr 9.
7
Regulation of plant root system architecture: implications for crop advancement.植物根系结构的调控:对作物改良的意义
Curr Opin Biotechnol. 2015 Apr;32:93-98. doi: 10.1016/j.copbio.2014.11.015. Epub 2014 Nov 29.
8
β-Amylase1 and β-amylase3 are plastidic starch hydrolases in Arabidopsis That Seem to Be Adapted for Different Thermal, pH, and stress conditions.β-淀粉酶1和β-淀粉酶3是拟南芥中的质体淀粉水解酶,似乎适应不同的温度、pH值和胁迫条件。
Plant Physiol. 2014 Dec;166(4):1748-63. doi: 10.1104/pp.114.246421. Epub 2014 Oct 7.
9
ABA-dependent and ABA-independent signaling in response to osmotic stress in plants.植物中响应渗透胁迫的脱落酸依赖型和脱落酸非依赖型信号传导
Curr Opin Plant Biol. 2014 Oct;21:133-139. doi: 10.1016/j.pbi.2014.07.009. Epub 2014 Aug 9.
10
Four Arabidopsis AREB/ABF transcription factors function predominantly in gene expression downstream of SnRK2 kinases in abscisic acid signalling in response to osmotic stress.四个拟南芥AREB/ABF转录因子主要在脱落酸信号转导的SnRK2激酶下游的基因表达中发挥作用,以响应渗透胁迫。
Plant Cell Environ. 2015 Jan;38(1):35-49. doi: 10.1111/pce.12351. Epub 2014 May 22.

脱落酸对叶片淀粉降解的调控对植物耐渗透胁迫至关重要。

Regulation of Leaf Starch Degradation by Abscisic Acid Is Important for Osmotic Stress Tolerance in Plants.

作者信息

Thalmann Matthias, Pazmino Diana, Seung David, Horrer Daniel, Nigro Arianna, Meier Tiago, Kölling Katharina, Pfeifhofer Hartwig W, Zeeman Samuel C, Santelia Diana

机构信息

Department of Plant and Microbial Biology, University of Zürich, 8008 Zürich, Switzerland.

Institute for Agricultural Sciences, ETH Zürich, 8092 Zürich, Switzerland.

出版信息

Plant Cell. 2016 Aug;28(8):1860-78. doi: 10.1105/tpc.16.00143. Epub 2016 Jul 19.

DOI:10.1105/tpc.16.00143
PMID:27436713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5006701/
Abstract

Starch serves functions that range over a timescale of minutes to years, according to the cell type from which it is derived. In guard cells, starch is rapidly mobilized by the synergistic action of β-AMYLASE1 (BAM1) and α-AMYLASE3 (AMY3) to promote stomatal opening. In the leaves, starch typically accumulates gradually during the day and is degraded at night by BAM3 to support heterotrophic metabolism. During osmotic stress, starch is degraded in the light by stress-activated BAM1 to release sugar and sugar-derived osmolytes. Here, we report that AMY3 is also involved in stress-induced starch degradation. Recently isolated Arabidopsis thaliana amy3 bam1 double mutants are hypersensitive to osmotic stress, showing impaired root growth. amy3 bam1 plants close their stomata under osmotic stress at similar rates as the wild type but fail to mobilize starch in the leaves. (14)C labeling showed that amy3 bam1 plants have reduced carbon export to the root, affecting osmolyte accumulation and root growth during stress. Using genetic approaches, we further demonstrate that abscisic acid controls the activity of BAM1 and AMY3 in leaves under osmotic stress through the AREB/ABF-SnRK2 kinase-signaling pathway. We propose that differential regulation and isoform subfunctionalization define starch-adaptive plasticity, ensuring an optimal carbon supply for continued growth under an ever-changing environment.

摘要

根据淀粉来源的细胞类型,淀粉发挥的功能在数分钟到数年的时间尺度上有所不同。在保卫细胞中,淀粉通过β-淀粉酶1(BAM1)和α-淀粉酶3(AMY3)的协同作用迅速被动员,以促进气孔开放。在叶片中,淀粉通常在白天逐渐积累,并在夜间被BAM3降解,以支持异养代谢。在渗透胁迫期间,淀粉在光照下通过应激激活的BAM1降解,以释放糖和糖衍生的渗透溶质。在这里,我们报道AMY3也参与应激诱导的淀粉降解。最近分离出的拟南芥amy3 bam1双突变体对渗透胁迫高度敏感,表现出根系生长受损。amy3 bam1植株在渗透胁迫下关闭气孔的速率与野生型相似,但无法在叶片中动员淀粉。¹⁴C标记显示,amy3 bam1植株向根部的碳输出减少,影响胁迫期间渗透溶质的积累和根系生长。通过遗传学方法,我们进一步证明脱落酸通过AREB/ABF-SnRK2激酶信号通路控制渗透胁迫下叶片中BAM1和AMY3的活性。我们提出,差异调节和同工型亚功能化定义了淀粉适应性可塑性,确保在不断变化的环境下为持续生长提供最佳碳供应。