RST31 通过调节细胞分裂素途径控制水稻(Oryza sativa)的耐盐性。

IF 6.1 2区 生物学 Q1 PLANT SCIENCES Plant Physiology and Biochemistry Pub Date : 2024-08-31 DOI:10.1016/j.plaphy.2024.109075
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引用次数: 0

摘要

盐胁迫会影响水稻的生长,从而降低谷物产量。然而,水稻对盐胁迫的响应机制还不完全清楚。与野生型(WT)植株相比,水稻耐盐 31(rst31)突变体在盐胁迫条件下表现出更长的芽和更大的干重。通过基于图谱的克隆和基因互补方法,我们确定 RST31 编码一个半尺寸 ABCG 转运蛋白 ABCG18。我们发现,突变 RST31 可减少盐胁迫下的 DNA 损伤,同时减少活性氧(ROS)的积累。RST31 的缺乏抑制了细胞分裂素从根到芽的转运,导致芽中细胞分裂素含量减少,根中细胞分裂素含量增加。外源反玉米素处理后,ROS在WT和rst31突变体植株中大量积累,降低了rst31对盐胁迫的耐受性。总之,我们的研究结果表明,在盐胁迫下,芽中的高细胞分裂素水平会导致 ROS 含量增加和严重的 DNA 损伤,从而导致对盐胁迫的敏感性降低。这些发现加深了我们对植物通过细胞分裂素途径应对盐胁迫的理解。
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RST31 controls salt tolerance in rice (Oryza sativa) by regulating the cytokinin pathway

Salt stress affects the growth of rice, which reduces grain yield. However, the mechanism of the rice response to salt stress is not fully understood. The rice salt tolerance 31 (rst31) mutant exhibits longer shoots and greater dry weight than wild type (WT) plants under salt stress conditions. Through map-based cloning and genetic complementation methods, we determined that RST31 encodes a half-size ABCG transporter protein, ABCG18. We showed that mutation of RST31 reduces DNA damage under salt stress, with less accumulation of reactive oxygen species (ROS). The deficiency of RST31 suppressed the root-to-shoot transport of cytokinin, which resulted in a decrease in cytokinin content in the shoot and an increase in cytokinin content in the root. ROS accumulated abundantly in WT and rst31 mutant plants after exogenous treatment with trans-zeatin, reducing rst31 tolerance of salt stress. Collectively, our results suggest that high cytokinin level in shoots leads to an increase in ROS content and severe DNA damage under salt stress, which lead to sensitivity to salt stress. These findings enhance our understanding of plant responses to salt stress through cytokinin pathways.

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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
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.
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