Qiuwei Lu , Shiting Bi , Suxuan Dong , Xueying Wang , Fuye Guo , Wenting Wang
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引用次数: 0
Abstract
Quinoa (Chenopodium quinoa Willd.), an emerging model species for abiotic stress tolerance due to its exceptional environmental resilience, exhibits unique molecular adaptations to combined low temperature-drought stress. However, the mechanism by which ABA enhances combined stress tolerance in quinoa remains elusive. This study characterized the abscisic acid (ABA)-mediated regulatory network in quinoa using integrated physiological and transcriptomics analyses. We demonstrated that combined stress triggers ABA accumulation via significant up-regulating NCED - ABA biosynthesis genes (log2(Fold Change) = 2.37 to 4.98, p < 0.05) while suppressing CYP707A - ABA catabolism genes (log2(Fold Change) = −1.81 to −2.99, p < 0.05). Exogenous ABA application under low temperature-drought stress activated the PYR/PYL-PP2C-SnRK2 cascade, thereby enhancing antioxidant defenses (SOD, POD, CAT) and increasing the ratio of soluble sugars to starch, which mitigated oxidative damage. The ABA-responsive antioxidant module (MEwhite, 110 genes), identified via WGCNA, coordinates redox homeostasis and carbohydrate metabolism. This module relies on HSF-centered transcriptional networks to enhance stress tolerance. This module integrates ERF and WRKY transcription factors to coordinate stress adaptation, concurrently enhancing antioxidant enzyme activity for ROS scavenging while maintaining metabolic equilibrium under combinatorial stress. Crucially, circadian rhythm genes (CRY, GI, PRR5) coordinates both ABA-dependent and ABA-independent pathways enhance stress adaptation, revealing crosstalk between stress signaling and biological clocks. Fluridone-mediated ABA suppression exacerbated the inhibition of oxidoreductase activity and soluble sugar content, confirming ABA's pivotal role. These findings provide mechanistic insights into ABA-driven combinatorial stress adaptation, offering targets for breeding climate-resilient crops.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.