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热休克蛋白 90 伴侣在正常和热胁迫条件下调节气孔分化。

HSP90 chaperones regulate stomatal differentiation under normal and heat stress conditions.

机构信息

Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University Olomouc , Olomouc, Czech Republic.

出版信息

Plant Signal Behav. 2020 Sep 1;15(9):1789817. doi: 10.1080/15592324.2020.1789817. Epub 2020 Jul 15.

DOI:10.1080/15592324.2020.1789817
PMID:32669038
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8550182/
Abstract

Stomatal development is tightly connected with the overall plant growth, while changes in environmental conditions, like elevated temperature, affect negatively stomatal formation. Stomatal ontogenesis follows a well-defined series of cell developmental transitions in the cotyledon and leaf epidermis that finally lead to the production of mature stomata. YODA signaling cascade regulates stomatal development mainly through the phosphorylation and inactivation of SPEECHLESS (SPCH) transcription factor, while HSP90 chaperones have a central role in the regulation of YODA cascade. Here, we report that acute heat stress affects negatively stomatal differentiation, leads to high phosphorylation levels of MPK3 and MPK6, and alters the expression of and transcription factors. Genetic depletion of HSP90 leads to decreased stomatal differentiation rates. Thus, HSP90 chaperones safeguard the completion of distinct stomatal differentiation steps depending on these two transcription factors under normal and heat stress conditions.

摘要

气孔发育与植物整体生长密切相关,而环境条件的变化,如温度升高,会对气孔形成产生负面影响。气孔发生遵循子叶和叶片表皮中一系列明确的细胞发育转变,最终导致成熟气孔的产生。YODA 信号级联主要通过 SPEECHLESS(SPCH)转录因子的磷酸化和失活来调节气孔发育,而 HSP90 伴侣在 YODA 级联的调节中起着核心作用。在这里,我们报告急性热应激会对气孔分化产生负面影响,导致 MPK3 和 MPK6 的磷酸化水平升高,并改变 和 转录因子的表达。HSP90 的遗传缺失会导致气孔分化率降低。因此,HSP90 伴侣在正常和热应激条件下,根据这两个转录因子,保障不同气孔分化步骤的完成。

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本文引用的文献

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YODA-HSP90 Module Regulates Phosphorylation-Dependent Inactivation of SPEECHLESS to Control Stomatal Development under Acute Heat Stress in Arabidopsis.YODA-HSP90 模块调节 SPEECHLESS 的磷酸化依赖性失活,以控制拟南芥在急性热胁迫下的气孔发育。
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Active BR signalling adjusts the subcellular localisation of BES1/HSP90 complex formation.活性 BR 信号调节 BES1/HSP90 复合物形成的亚细胞定位。
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