由细胞分裂素和非生物胁迫反应组成的初级多步磷酸连锁激活:从芸薹属 A 型响应调节因子的比较分析中获得的启示。

IF 5.6 2区 生物学 Q1 PLANT SCIENCES
Katrina Leslie Nicolas Mala, Jan Skalak, Elena Zemlyanskaya, Vladislav Dolgikh, Veronika Jedlickova, Helene S Robert, Lenka Havlickova, Klara Panzarova, Martin Trtilek, Ian Bancroft, Jan Hejatko
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引用次数: 0

摘要

多步磷酸循环(MSP)信号整合了激素和环境信号,可控制植物的生长发育和适应性反应。A 型响应调节因子(RRAs)、MSP 级联的下游成员和细胞分裂素一级响应基因应该主要介导(细胞分裂素诱导的)MSP 信号转导的负反馈调节。然而,转录数据表明,RRAs 也参与了胁迫相关反应。通过与表征良好的拟南芥RRAs的进化保守性比较,我们在甘蓝和油菜中分别发现了5个和38个新的推测RRAs。我们的系统发育分析表明,在十字花科植物的进化过程中,存在着基因特异性选择压力,使 ARR3、ARR6 和 ARR16 的同源物保持为单体。我们根据细胞分裂素介导的上调动力学对 RRAs 进行了分类,并观察到芸苔属各物种在这类反应中的相似性和特异性。利用生物信息学分析和实验数据证明了源于大连芸苔属的 TCSv2 报告基因对细胞分裂素和非生物胁迫的响应性,我们揭示了细胞分裂素和胁迫介导的 RRAs 在芸苔属和油菜属植物中上调的机理。值得注意的是,我们发现冷胁迫诱导的 RRA 转录部分依赖于细胞分裂素,从而证实了细胞分裂素信号在作物适应性反应中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary multistep phosphorelay activation comprises both cytokinin and abiotic stress responses: insights from comparative analysis of Brassica type-A response regulators.

Multistep phosphorelay (MSP) signaling integrates hormonal and environmental signals to control both plant development and adaptive responses. Type-A RESPONSE REGULATOR (RRA) genes, the downstream members of the MSP cascade and cytokinin primary response genes, are thought to mediate primarily the negative feedback regulation of (cytokinin-induced) MSP signaling. However, transcriptional data also suggest the involvement of RRA genes in stress-related responses. By employing evolutionary conservation with the well-characterized Arabidopsis thaliana RRA genes, we identified five and 38 novel putative RRA genes in Brassica oleracea and Brassica napus, respectively. Our phylogenetic analysis suggests the existence of gene-specific selective pressure, maintaining the homologs of ARR3, ARR6, and ARR16 as singletons during the evolution of Brassicaceae. We categorized RRA genes based on the kinetics of their cytokinin-mediated up-regulation and observed both similarities and specificities in this type of response across Brassicaceae species. Using bioinformatic analysis and experimental data demonstrating the cytokinin and abiotic stress responsiveness of the A. thaliana-derived TCSv2 reporter, we unveil the mechanistic conservation of cytokinin- and stress-mediated up-regulation of RRA genes in B. rapa and B. napus. Notably, we identify partial cytokinin dependency of cold stress-induced RRA transcription, thus further demonstrating the role of cytokinin signaling in crop adaptive responses.

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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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