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[参与抗病性的克隆及功能分析]

[Cloning and functional analysis of involved in disease resistance].

作者信息

Fu Jiahui, Zuo Lin, Huang Weiqun, Sun Song, Guo Liangyu, Hu Min, Lu Peilan, Lin Shanshan, Liang Kangjing, Sun Xinli, Jia Qi

机构信息

Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops, College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China.

Key Laboratory of Crop Ecology and Molecular Physiology, Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2025 Jul 25;41(7):2803-2817. doi: 10.13345/j.cjb.250168.

Abstract

The plant F-box protein more axillary growth 2 (MAX2) is a key factor in the signal transduction of strigolactones (SLs) and karrinkins (KARs). As the main component of the SKP1-CUL1-FBX (SCF) complex ubiquitin ligase E3, MAX2 is responsible for specifically recognizing the target proteins, suppressor of MAX2 1/SMAX1-like proteins (SMAX1/SMXLs), which would be degraded after ubiquitination. It can thereby regulate plant morphogenesis and stress responses. There exist homologous genes of in the important grain and oil crop soybean (). However, its role in plant defense responses has not been investigated yet. Here, , a homologous gene of , was successfully cloned from stressed soybean. Bioinformatics analysis revealed that there were two homologous genes, and , with a similarity of 96.2% in soybean. Their F-box regions were highly conserved. The sequence alignment and cluster analysis of plant MAX2 homologous proteins basically reflected the evolutionary relationship of plants and also suggested that soybean MAX2 might be a multifunctional protein. Expression analysis showed that plant pathogen infection and salicylic acid treatment induced the expression of in soybean, which is consistent with that of in . Ectopic expression of compensated for the susceptibility of mutant to pathogen, indicating that positively regulated plant disease resistance. In addition, yeast two hybrid technology was used to explore the potential target proteins of . The results showed that interacted with SMXL6 and weakly interacted with SMXL2. In summary, is a positive regulator in plant defense responses, and its expression is induced by pathogen infection and salicylic acid treatment. might exert its effect through interaction with SMXL6 and SMXL2. This study expands the theoretical exploration of soybean disease resistant F-box and provides a scientific basis for future soybean disease resistant breeding.

摘要

植物F-box蛋白多腋生生长2(MAX2)是独脚金内酯(SLs)和 karrikins(KARs)信号转导的关键因子。作为SKP1-CUL1-FBX(SCF)复合体泛素连接酶E3的主要成分,MAX2负责特异性识别靶蛋白,即MAX2的抑制因子1/SMAX1样蛋白(SMAX1/SMXLs),这些蛋白在泛素化后会被降解。从而它可以调节植物形态发生和应激反应。在重要粮油作物大豆(Glycine max)中存在MAX2的同源基因。然而,其在植物防御反应中的作用尚未得到研究。在此,从受胁迫的大豆中成功克隆了MAX2的同源基因GmMAX2。生物信息学分析表明,大豆中有两个MAX2同源基因GmMAX2a和GmMAX2b,相似度为96.2%。它们的F-box区域高度保守。植物MAX2同源蛋白的序列比对和聚类分析基本反映了植物的进化关系,也表明大豆MAX2可能是一种多功能蛋白。表达分析表明,植物病原体感染和水杨酸处理可诱导大豆中GmMAX2的表达,这与拟南芥中AtMAX2的情况一致。GmMAX2的异位表达弥补了Atmax2突变体对病原体的易感性,表明GmMAX2正向调节植物抗病性。此外,利用酵母双杂交技术探索了GmMAX2的潜在靶蛋白。结果表明,GmMAX2与SMXL6相互作用,与SMXL2弱相互作用。综上所述,GmMAX2是植物防御反应中的正向调节因子,其表达受病原体感染和水杨酸处理诱导。GmMAX2可能通过与SMXL6和SMXL2相互作用发挥作用。本研究拓展了大豆抗病F-box的理论探索,为未来大豆抗病育种提供了科学依据。

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