Erokhin Denis, Baranova Diana, Sergeeva Ksenia, Pasechnik Tatiana, Shcherbakova Larisa, Statsyuk Natalia, Dzhavakhiya Vitaly
All-Russian Research Institute of Phytopathology, 143050 Bolshie Vyazemy, Russia.
Int J Mol Sci. 2024 Dec 3;25(23):13015. doi: 10.3390/ijms252313015.
The ability of a cold-shock protein CspD from to protect both dicots and monocots against various pathogens is well confirmed under both greenhouse and field conditions; however, the molecular basis of this phenomenon at the transcriptomic level still remains unexplored. Expression profiles of some marker genes associated with SAR/ISR nonspecific resistance pathways and ROS scavengers were examined in CspD-treated plants, and the RNA-seq analysis of CspD-treated plants was first carried out. The ISR markers PDF1.2 and PR4 were overexpressed locally in treated tobacco leaves with the maximum 2.4- and 5.7-fold change, respectively, reached 12 h after the leaf treatment with CspD; PDF1.2 was also up-regulated 4.8-fold four days after the inoculation of treated plants with TMV. The ROS scavenger analysis demonstrated overexpression of Cu-Zn superoxide dismutase in both treated (with the maximum 5.4-fold change observed 6 h after the treatment) leaves and leaves from the upper tier ("system" leaves, 6.5-fold change observed 4 days after the treatment). The ROS assay confirmed endogenous accumulation of superoxide in CspD-treated leaves 6 and 24 h after the treatment. An in silico comparative study of orthologs of highly up-regulated tobacco genes induced by CspD with genes activated by some other molecular patterns revealed the specific CspD-induced expression of Cu-Zn superoxide dismutase and some other genes associated with light and cold responses. This study may contribute to a better understanding of cross-talking between abiotic stress and nonspecific immunity in plants.
来自[具体来源未提及]的冷休克蛋白CspD在温室和田间条件下均能有效保护双子叶植物和单子叶植物免受多种病原体侵害,这一点已得到充分证实;然而,在转录组水平上,这一现象的分子基础仍未得到探索。我们检测了CspD处理的[植物名称未提及]植物中一些与系统获得性抗性/诱导性系统抗性非特异性抗性途径及活性氧清除剂相关的标记基因的表达谱,并首次对CspD处理的植物进行了RNA测序分析。在CspD处理烟草叶片后12小时,诱导性系统抗性标记基因PDF1.2和PR4在局部过表达,变化倍数分别达到最大值2.4倍和5.7倍;在用烟草花叶病毒接种处理过的植物4天后,PDF1.2也上调了4.8倍。活性氧清除剂分析表明,铜锌超氧化物歧化酶在处理后的叶片(处理后6小时观察到最大变化倍数为5.4倍)和上层叶片(“系统”叶片,处理后4天观察到变化倍数为6.5倍)中均过表达。活性氧检测证实,在CspD处理后的叶片中,处理后6小时和24小时内超氧化物有内源性积累。一项计算机模拟比较研究将CspD诱导的烟草高度上调基因的直系同源基因与其他一些分子模式激活的[植物名称未提及]基因进行了对比,结果揭示了铜锌超氧化物歧化酶以及其他一些与光和冷反应相关基因的特异性CspD诱导表达。这项研究可能有助于更好地理解植物中非生物胁迫与非特异性免疫之间的相互作用。