Rice OsCIPK17-OsCBL2/3 module enhances shoot Na+ exclusion and plant salt tolerance in transgenic Arabidopsis

IF 6.1 2区 生物学 Q1 PLANT SCIENCES
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Abstract

Soil salinity is detrimental to plant growth and remains a major threat to crop productivity of the world. Plants employ various physiological and molecular mechanisms to maintain growth under salt stress. Identification of genes and genetic loci underlying plant salt tolerance holds the key to breeding salt tolerant crops. CIPK-CBL pathways regulate adaptive responses of plants (especially ion transport) to abiotic stresses via fine-tuned Ca2+ signal transduction. In this study, we showed that over-expression of OsCIPK17 in Arabidopsis enhanced primary root elongation under salt stress, which is in a Ca2+ dependent manner. Further investigation revealed that, under salt stress, OsCIPK17 transcript level was significantly induced and its protein moved from the cytosol to the tonoplast. Using both Y2H and BiFC, tonoplast-localised OsCBL2 and OsCBL3 were shown to interact with OsCIPK17. Interestingly, over-expressing salt-induced OsCBL2 or OsCBL3 in Arabidopsis led to enhanced primary root elongation under salt stress. In this process, OsCIPK17 was shown recruited to the tonoplast (similar to the effect of salt stress). Furthermore, transgenic Arabidopsis lines individually over-expressing OsCIPK17, OsCBL2 and OsCBL3 all demonstrated larger biomass and less Na + accumulation in the shoot under salt stress. All data combined suggest that OsCIPK17- OsCBL2/3 module is a major component of shoot Na+ exclusion and therefore plant salt tolerance, which is through enhanced Na + compartmentation into the vacuole in the root. OsCIPK17 and OsCBL2/3 are therefore potential genetic targets that can be used for delivering salt tolerant rice cultivars.

水稻 OsCIPK17-OsCBL2/3 模块可增强转基因拟南芥芽的 Na+ 排阻和植物耐盐性
土壤盐分不利于植物生长,仍然是全球作物生产力的主要威胁。植物利用各种生理和分子机制来维持盐胁迫下的生长。鉴定植物耐盐基因和遗传位点是培育耐盐作物的关键。CIPK-CBL 通路通过微调 Ca2+ 信号转导调节植物对非生物胁迫的适应性反应(尤其是离子转运)。在这项研究中,我们发现在拟南芥中过度表达 OsCIPK17 能增强其在盐胁迫下的主根伸长,而这是一种 Ca2+ 依赖性方式。进一步研究发现,在盐胁迫下,OsCIPK17的转录水平被显著诱导,其蛋白质也从细胞质转移到了营养体。利用Y2H和BiFC技术,结果表明定位于细胞质的OsCBL2和OsCBL3与OsCIPK17相互作用。有趣的是,在拟南芥中过量表达盐诱导的 OsCBL2 或 OsCBL3 会导致主根在盐胁迫下伸长增强。在这一过程中,OsCIPK17 被招募到了营养体(与盐胁迫的效果类似)。此外,单独过度表达 OsCIPK17、OsCBL2 和 OsCBL3 的转基因拟南芥品系在盐胁迫下都表现出较大的生物量和较少的芽中 Na + 累积。所有数据综合表明,OsCIPK17- OsCBL2/3 模块是芽Na+排斥的主要组成部分,因此也是植物耐盐性的主要组成部分。因此,OsCIPK17 和 OsCBL2/3 是潜在的遗传靶标,可用于培育耐盐水稻品种。
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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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