Thalmann Matthias, Pazmino Diana, Seung David, Horrer Daniel, Nigro Arianna, Meier Tiago, Kölling Katharina, Pfeifhofer Hartwig W, Zeeman Samuel C, Santelia Diana
Department of Plant and Microbial Biology, University of Zürich, 8008 Zürich, Switzerland.
Institute for Agricultural Sciences, ETH Zürich, 8092 Zürich, Switzerland.
Plant Cell. 2016 Aug;28(8):1860-78. doi: 10.1105/tpc.16.00143. Epub 2016 Jul 19.
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.
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。