OsCaM1-OsCAMTA1模块通过增强水稻靶基因OsDREB1B和OsCML16的转录本来增强耐盐性

IF 5.7 1区 生物学 Q1 PLANT SCIENCES
Shuang Liu, Shoumin Wang, Yuying Zheng, Panpan Zhao, Hongpei Jin, Guosheng Xie
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引用次数: 0

摘要

盐胁迫诱导植物细胞质钙离子(Ca2+)峰值,激活Ca2+/钙调蛋白(CaM)信号。钙调素结合转录激活因子(CAMTAs)是Ca2+/ cam介导的非生物应激反应的关键组成部分。然而,Ca2+/CaM如何与OsCAMTAs家族成员特异性相互作用以调节水稻的耐盐性在很大程度上尚未确定。通过综合分子遗传学,生化和生理分析,我们证明了OsCaM1/2/3与OsCAMTA1/2/4/6以Ca2+依赖的方式特异性相互作用。转基因表明OsCaM1-1和OsCAMTA1增强了水稻的耐盐性。oscamta1细胞系的rna序列(RNA-seq)分析表明,oscamta1通过协调涉及Ca2+结合、激素反应、转录调控和盐胁迫途径的下游靶点,积极调节盐耐受性。双荧光素酶(LUC)检测发现,OsCaM1分别激活OsCAMTA1对靶点OsDREB1B和OsCML16的转录活性,这两个靶点都对水稻幼苗的耐盐性具有正向调节作用。转录组学筛选显示,OsCAMTA1和OsDREB1B在盐胁迫下共调控OsZFP179、OsMST4和Oshox22基因,OsCAMTA1和OsCML16在盐胁迫下共调控OsP5CS、OsABI5-1和OsHAK24基因。我们的研究发现了一个新的OsCaM1-OsCAMTA1模块,可以调节盐胁迫下OsDREB1B/OsCML16转录级联,为未来培育盐适应水稻品种提供候选基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The OsCaM1-OsCAMTA1 module confers salinity tolerance by enhancing transcripts of the targets OsDREB1B and OsCML16 in rice

Salt stress induces cytoplasmic calcium (Ca2+) ion spikes and activates Ca2+/ calmodulin (CaM) signaling in plant cells. Calmodulin-binding transcription activators (CAMTAs) are pivotal components of Ca2+/CaM-mediated abiotic stress responses. Nevertheless, how Ca2+/CaM specifically interacts with the OsCAMTAs family members to modulate salinity tolerance is largely undetermined in rice. Through integrated molecular genetics, biochemical, and physiological analyses, we demonstrated that OsCaM1/2/3 interacted specifically with OsCAMTA1/2/4/6 in a Ca2+-dependent manner. Transgenics showed OsCaM1-1 and OsCAMTA1 enhanced salinity tolerance in rice. RNA-sequence (RNA-seq) profiling of oscamta1 lines suggested that OsCAMTA1 positively regulates salinity tolerance by orchestrating downstream targets involved in Ca2+ binding, hormonal responses, transcriptional regulation, and salt stress pathways. The dual-luciferase (LUC) assays identified that OsCaM1 activates the transcriptional activity of OsCAMTA1 to the targets OsDREB1B and OsCML16, respectively, both of which positively regulate the salinity tolerance in rice seedlings. Transcriptomic screening revealed that OsCAMTA1 and OsDREB1B co-regulated the genes OsZFP179, OsMST4, and Oshox22, while OsCAMTA1 and OsCML16 co-regulated the genes OsP5CS, OsABI5-1, and OsHAK24 under salt stress. Our study reveals a novel OsCaM1-OsCAMTA1 module to regulate the OsDREB1B/OsCML16 transcriptional cascade under salt stress, providing candidate genes for breeding salt-adapted rice varieties in the future.

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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
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