外源褪黑激素通过调节蚕豆萌芽期苯丙类生物合成途径增强耐盐性

IF 6.8 Q1 PLANT SCIENCES
Qi Zhang , Anjian Li , Bo Xu , Hongda Wang , Jinqi Yu , Jiaxi Liu , Lingmin Jian , Cheng Quan , Jidao Du
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引用次数: 0

摘要

盐胁迫是一种主要的非生物环境胁迫因素。植物从发芽开始就能感受到盐分,从而对其生长和发育产生负面影响。鉴于农作物在萌芽阶段是遭遇胁迫的第一个阶段,因此在萌芽阶段提高耐盐性至关重要。褪黑激素(N-乙酰-5-甲氧基色胺)是一种强效抗氧化剂,可以缓解各种环境因素带来的压力。本研究以普通豆类品种 "黑云豆 "为植物材料。选择 70 mMol-L-1 NaCl 浓度作为胁迫处理,并施加 100 μmol-L-1 褪黑激素。共设立了四个处理组:CK(对照组,水处理)、S(盐胁迫)、M(褪黑激素)和 M+S(盐胁迫加褪黑激素)。与盐胁迫组(S)相比,在盐胁迫下施用褪黑素(M+S)能显著改善萌芽长度、表面积、体积和平均直径。生理学分析表明,盐胁迫增加了活性氧(ROS)清除酶的活性,而外源褪黑激素(M+S)进一步增强了这种活性。盐胁迫还明显提高了丙二醛(MDA)、过氧化氢(H2O2)和超氧阴离子(O2-)等胁迫标志物的水平。然而,在 M+S 处理下,这些标志物都有所下降,这表明褪黑激素具有保护作用。RNA测序(RNA-Seq)分析在对照组(W)和盐胁迫组(S)之间发现了639个差异表达基因(DEGs),在盐胁迫组(S)和添加褪黑激素的盐胁迫组(M+S)之间发现了170个差异表达基因(DEGs)。两个比较组共有 40 个 DEGs(Co-DEGs)。基因本体(GO)富集分析表明,氧化还原酶活性(GO:0016491)和氧化还原过程(GO:0055114)在所有三组(WvsS 组、SvsM+S 组和 Co-DEGs 组)中都有富集。京都基因组百科全书》(KEGG)通路分析表明,苯丙类生物合成(Ko00940)是所有三个组中最富集的通路。在这一途径中,4-香豆酸-CoA 连接酶(4CL)和过氧化物酶(POD)被确定为关键酶。分子对接模拟进一步证实了褪黑素与这两种酶的结合潜力。此外,4CL 活性和木质素含量分析支持苯丙类生物合成是褪黑激素保护作用的基本机制。总之,这些发现为应用褪黑激素提高普通豆类作物的耐盐性提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exogenous melatonin enhances salt tolerance by regulating the phenylpropanoid biosynthesis pathway in common bean at sprout stage

Salt stress is a major environmental abiotic stress factor. Plants sense salt from germination onwards, negatively affecting their growth and development. Enhancing salt tolerance in crops at the sprout stage is crucial, given that it is the first stage to encounter stress. Melatonin (N-acetyl-5-methoxytryptamine) is a potent antioxidant that can alleviate stress from various environmental factors. Here, a common bean variety “Heiyundou” was used as the plant material. A concentration of 70 mMol·L−1 NaCl was chosen as the stress treatment, and 100 μmol·L−1 melatonin was applied. Four treatment groups were established: CK (control, water treatment), S (salt stress), M (melatonin), and M+S (salt stress with melatonin). Melatonin application under salt stress (M+S) significantly improved sprout length, surface area, volume, and average diameter compared to the salt stress group (S). Physiological analysis revealed that salt stress increased the activity of reactive oxygen species (ROS) scavenging enzymes, while exogenous melatonin (M+S) further enhanced this activity. Salt stress also significantly elevated levels of stress markers like malondialdehyde (MDA), hydrogen peroxide (H2O2), and superoxide anion (O2). However, these markers decreased under the M+S treatment, indicating melatonin's protective effect. RNA sequencing (RNA-Seq) analysis identified 639 differentially expressed genes (DEGs) between the control (W) and salt stress (S) groups, and 170 DEGs between the salt stress (S) and salt stress with melatonin (M+S) groups. 40 DEGs were common to both comparisons (Co-DEGs). Gene Ontology (GO) enrichment analysis revealed that oxidoreductase activity (GO:0016491) and oxidation–reduction processes (GO:0055114) were enriched in all three groups (WvsS, SvsM+S, and Co-DEGs). Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that phenylpropanoid biosynthesis (Ko00940) was the most enriched pathway in all three groups. Within this pathway, 4-coumarate-CoA ligase (4CL) and peroxidase (POD) were identified as key enzymes. Molecular docking simulations further confirmed the binding potential of melatonin to these two enzymes. Additionally, 4CL activity and lignin content analyses supported the role of phenylpropanoid biosynthesis as the underlying mechanism of melatonin's protective action. Collectively, these findings provide a theoretical basis for applying melatonin in enhancing salt tolerance in common bean crops.

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来源期刊
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
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