在十字花科植物中,主要的多步磷接力激活包括细胞分裂素和非生物胁迫响应

Katrina Leslie Nicolas Mala, Jan Skalak, Elena Zemlyanskaya, Vladislav Dolgikh, Veronika Jedlickova, Helene Robert-Boisivon, Lenka Havlickova, Klara Panzarova, Martin Trtilek, Ian Bancroft, Jan Hejatko
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摘要

多步磷接力(Multistep phosphorelay, MSP)信号通过整合激素和环境信号来控制植物的发育和适应性反应。a型反应调节因子(type-A RESPONSE REGULATORs, RRAs)是MSP级联的下游成员和细胞分裂素一级反应基因,被认为主要介导(细胞分裂素诱导的)MSP信号的负反馈调节。然而,转录数据表明RRAs也参与应激相关反应。通过对拟南芥RRAs的进化保守分析,我们在甘蓝和甘蓝型油菜中分别鉴定出5个和38个新的推测RRAs。我们的系统发育分析表明,在甘蓝和油菜的进化过程中,存在基因特异性的选择压力,使ARR3、ARR6和ARR16的同源基因保持为单基因。我们根据细胞分裂素介导的上调动力学对RRAs进行了分类,并观察了十字花科植物中这种反应的相似性和特异性。利用生物信息学分析和实验数据证明了拟南芥来源的TCSv2报告细胞分裂素的响应性,我们揭示了细胞分裂素介导的RRAs上调在油菜和甘蓝型油菜中的机制保护。值得注意的是,我们发现冷胁迫诱导的RRA转录部分依赖细胞分裂素,从而证实了细胞分裂素信号在作物适应性反应中的作用。
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Primary multistep phosphorelay activation comprises both cytokinin and abiotic stress responses in Brassicaceae
Multistep phosphorelay (MSP) signaling integrates hormonal and environmental signals to control plant development and adaptive responses. The type-A RESPONSE REGULATORs (RRAs), the downstream members of the MSP cascade and cytokinin primary response genes, are supposed to mediate primarily the negative feedback regulation of (cytokinin-induced) MSP signaling. However, the transcriptional data suggest the involvement of RRAs in stress-related responses as well. By employing evolutionary conservation with the well-characterized Arabidopsis thaliana RRAs, we identified 5 and 38 novel putative RRAs 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 Brassica oleracea and Brassica rapa. We categorized RRAs based on the kinetics of their cytokinin-mediated upregulation and observed both similarities and specificities in this type of response across Brassicaceae. Using bioinformatic analysis and experimental data demonstrating the cytokinin responsiveness of Arabidopsis-derived TCSv2 reporter, we unveil the mechanistic conservation of cytokinin-mediated upregulation of RRAs in Brassica rapa and Brassica napus. Notably, we identify partial cytokinin dependency of cold stress-induced RRA transcription, thus corroborating the role of cytokinin signaling in the crop adaptive responses.
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