油菜素内酯介导的BraSERKs调控和抗氧化防御增强使大白菜耐Cd/Zn胁迫。

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Shaohui Yang, Ying Chu, Chen Wang, Ziyi Liu, Jiehua Wang
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引用次数: 0

摘要

体细胞胚胎发生受体激酶(SERKs)是植物发育和逆境适应的关键调控因子,已知其整合多种信号通路,包括油菜素内酯(BR)介导的反应,协调调节逆境相关基因的表达。虽然SERKs参与生物/非生物胁迫调节,但它们在重金属(HM)胁迫反应和br介导的重金属暴露下的转录控制中的作用仍未被探索。因此,我们系统地鉴定了中国大白菜(Brassica rapa subsp)中20个BraSERK基因。揭示了保守的结构域结构和应激反应表达模式。3个BraSERK成员(BraSERK9、12和17)在Cd/Zn胁迫下表现出显著的诱导作用。采用外源喷施24-表油菜素内酯(EBR)的方法,研究了油菜素内酯对Cd/Zn胁迫下大白菜的潜在调控作用。结果表明,EBR能显著提高叶绿素总含量,降低Zn/Cd转运,增强抗氧化能力,从而减弱Cd/Zn的毒性。此外,EBR以组织和金属特异性的方式动态调节BraSERKs的表达,增强了zn胁迫芽中BraSERK12/17的诱导,同时抑制了BraSERK9。我们的研究结果表明,breserks可能有助于br介导的HM适应,而EBR似乎通过Cd/Zn共胁迫条件下的直接植物保护和SERK通路活性的潜在调节发挥双重保护作用。这项研究促进了我们对br介导的作物金属耐受性的理解,提供了通过靶向SERK通路调节减轻HM毒性的潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brassinosteroid-Mediated BraSERKs Regulation and Antioxidant Defense Enhancement Confer Cd/Zn Stress Tolerance in Chinese Cabbage.

Somatic embryogenesis receptor kinases (SERKs) are pivotal regulators of plant development and stress adaptation, known to integrate multiple signaling pathways, including brassinosteroid (BR)-mediated responses to coordinately modulate stress-related gene expression. While SERKs participate in biotic/abiotic stress regulation, their roles in heavy metal (HM) stress responses and BR-mediated transcriptional control under HM exposure remain unexplored. Therefore, we systematically identified 20 BraSERK genes in Chinese cabbage (Brassica rapa subsp. Pekinensis), revealing conserved domain architectures and stress-responsive expression patterns. Three BraSERK members (BraSERK9, 12, and 17) exhibited significant induction under Cd/Zn stress. The potential regulatory roles of BR on Chinese cabbage exposed to Cd/Zn stress were investigated in this study by exogenous spraying of 24-epibrassinolide (EBR). The results showed that EBR could significantly increase total chlorophyll content, reduce Zn/Cd translocation, increase antioxidant capacity, and thus attenuate Cd/Zn-induced toxicity. Moreover, EBR dynamically regulated BraSERKs expression in a tissue- and metal-specific manner, potentiating BraSERK12/17 induction in Zn-stressed shoots while suppressing BraSERK9. Our findings suggest that BraSERKs may contribute to BR-mediated HM adaptation, while EBR appears to play a dual protective role through both direct phytoprotection and potential modulation of SERK pathway activity under Cd/Zn co-stress conditions. This study advances our understanding of BR-mediated metal tolerance in crops, offering potential strategies to mitigate HM toxicity through targeted SERK pathway modulation.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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