Dynamic transcriptomics and physiological insights reveal multi-tissue salt adaptation mechanisms in Amaranthus hypochondriacus across stress gradients.
Qian Xu, Jinxin Gan, Zhikang Zhou, Tao Zhou, Rui Lu, Ningfang Liu, Longxing Hu
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引用次数: 0
Abstract
Key message: Transcriptomic and physiological analyses identified key salt-responsive pathways and genes in Amaranthus hypochondriacus under 100/250 mM NaCl stress. Soil salinization critically threatens crop productivity, necessitating the exploration of salt-tolerant species. Amaranthus hypochondriacus, recognized as a salt-tolerant grain species, exhibits distinct adaptive mechanisms under moderate (100 mM NaCl) and severe (250 mM NaCl) salinity based on the integrated physiological and multi-tissue transcriptomic analyses. Under moderate salt stress, physiological and transcriptomic analyses revealed three key tolerance strategies: rapid ABA signaling activation (e.g., NCED [9-cis-epoxycarotenoid dioxygenase] upregulation within 6 h exposure to salt stress), sustained leaf ion homeostasis (unchanged leaf Na⁺/K⁺ ratio), and tenfold root proline accumulation. Severe stress triggered osmotic imbalance (89% reduced stomatal conductance), ionic toxicity (24-fold elevated leaf Na⁺/K⁺ ratio), and oxidative damage (fivefold elevated leaf relative electrical conductivity) despite upregulated glutathione biosynthesis. Notably, A. hypochondriacus uniquely maintained DNA stability via enriched DNA repair pathways (e.g., homologous recombination) and transcriptional induction of replication-related gene. The WGCNA analysis identified multiple salt tolerance-associated key candidate genes, including the proline biosynthesis genes (P5CS [pyrroline-5-carboxylate synthetase] and P5CR [pyrroline-5-carboxylate reductase]), as well as the ion transporter genes (NHX [Na+/K+ antiporter] for sequestration of Na+ into vacuoles and SOS1 [Salt Overly Sensitive 1] for extrusion of Na⁺ out of cells). Clustering of 1,578 transcription factors (TFs) identified six expression clusters, with root-specific ERF/MYB activation and leaf-enriched WRKY/C3H induction. This study elucidated the conserved salt tolerance strategies of grain amaranths, emphasizing its dual-phase adaptation: osmotic/ionic homeostasis under moderate stress and DNA stability maintenance under severe stress, orchestrated by lineage-specific TF networks. These findings provide critical insights for improving crop resilience in saline environments.
通过转录组学和生理分析,确定了苋属植物在100/250 mM NaCl胁迫下的关键盐响应途径和基因。土壤盐碱化严重威胁作物生产力,因此有必要探索耐盐物种。综合生理和多组织转录组学分析结果显示,苋属耐盐籽粒植物在中度(100 mM NaCl)和重度(250 mM NaCl)盐胁迫下表现出不同的适应机制。在中等盐胁迫下,生理和转录组学分析揭示了三个关键的耐受策略:ABA信号的快速激活(如NCED[9-顺式-环氧类胡萝卜素双加氧酶]在盐胁迫下6小时内上调),持续的叶片离子稳态(叶片Na + /K +比例不变),以及10倍的根脯氨酸积累。尽管谷胱甘肽的生物合成上调,但严重的应激会引发渗透失衡(气孔导度降低89%)、离子毒性(叶片Na + /K +比升高24倍)和氧化损伤(叶片相对电导率升高5倍)。值得注意的是,软肋刺通过丰富的DNA修复途径(如同源重组)和复制相关基因的转录诱导,独特地维持了DNA的稳定性。WGCNA分析发现了多个与盐耐性相关的关键候选基因,包括脯氨酸生物合成基因(P5CS[吡咯-5-羧酸合成酶]和P5CR[吡咯-5-羧酸还原酶]),以及离子转运基因(NHX [Na+/K+反转运蛋白],用于将Na+隔离到液泡中,SOS1[盐过度敏感1]用于将Na+挤出细胞)。对1578个转录因子(TFs)的聚类鉴定出6个表达簇,具有根特异性的ERF/MYB激活和叶片富集的WRKY/C3H诱导。本研究阐明了粒苋菜的保守耐盐策略,强调了其双相适应:中等胁迫下的渗透/离子稳态和严重胁迫下的DNA稳定性维持,这是由谱系特异性TF网络协调的。这些发现为提高作物在盐碱化环境中的抗逆性提供了重要见解。
期刊介绍:
Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as:
- genomics and genetics
- metabolism
- cell biology
- abiotic and biotic stress
- phytopathology
- gene transfer and expression
- molecular pharming
- systems biology
- nanobiotechnology
- genome editing
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The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.