Guo Huan, Wang Jianfeng, Yao Di, Yu Ligang, Jiang Wenting, Xie Lincai, Lv Shikai, Zhang Xiangyu, Wang Yajuan, Wang Changyou, Ji Wanquan, Zhang Hong
State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Agronomy, Northwest A & F University, Yangling, Shaanxi, 712100, China.
State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Plant Protection, Northwest A & F University, Yangling, Shaanxi, 712100, China.
Stress Biol. 2024 Jun 11;4(1):29. doi: 10.1007/s44154-024-00163-z.
In eukaryotes, the nuclear membrane that encapsulates genomic DNA is composed of an inner nuclear membrane (INM), an outer nuclear membrane (ONM), and a perinuclear space. SUN proteins located in the INM and KASH proteins in the ONM form the SUN-KASH NM-bridge, which functions as the junction of the nucleocytoplasmic complex junction. Proteins containing the SUN domain showed the highest correlation with differentially accumulated proteins (DAPs) in the wheat response to fungal stress. To understand the characteristics of SUN and its associated proteins in wheat responding to pathogen stress, here we investigated and comprehensive analyzed SUN- and KASH-related proteins among the DAPs under fungi infection based on their conserved motifs. In total, four SUN proteins, one WPP domain-interacting protein (WIP), four WPP domain-interacting tail-anchored proteins (WIT), two WPP proteins and one Ran GTPase activating protein (RanGAP) were identified. Following transient expression of Nicotiana benthamiana, TaSUN2, TaRanGAP2, TaWIT1 and TaWIP1 were identified as nuclear membrane proteins, while TaWPP1 and TaWPP2 were expressed in both the nucleus and cell membrane. RT-qPCR analysis demonstrated that the transcription of TaSUN2, TaRanGAP2 and TaWPP1 were strongly upregulated in response to fungal infection. Furthermore, using the bimolecular fluorescence complementation, the luciferase complementation and a nuclear and split-ubiquitin-based membrane yeast two-hybrid systems, we substantiated the interaction between TaSUN2 and TaWIP1, as well as TaWIP1/WIT1 and TaWPP1/WPP2. Silencing of TaSUN2, TaRanGAP2 and TaWPP1 in wheat leaves promoted powdery mildew infection and hyphal growth, and reduced the expression of TaBRI1, TaBAK1 and Ta14-3-3, indicating that these NM proteins play a positive role in resistance to fungal stress. Our study reveals the characteristics of NM proteins and propose the preliminary construction of SUN-WIP-WPP-RanGAP complex in wheat, which represents a foundation for detail elucidating their functions in wheat in future.
在真核生物中,包裹基因组DNA的核膜由内核膜(INM)、外核膜(ONM)和核周间隙组成。位于INM的SUN蛋白和ONM的KASH蛋白形成SUN-KASH核膜桥,其作为核质复合体连接的连接点发挥作用。含有SUN结构域的蛋白质与小麦对真菌胁迫反应中差异积累蛋白(DAP)的相关性最高。为了解小麦在响应病原体胁迫时SUN及其相关蛋白的特征,在此我们基于其保守基序,对真菌感染下DAP中的SUN和KASH相关蛋白进行了研究和综合分析。总共鉴定出4种SUN蛋白、1种WPP结构域相互作用蛋白(WIP)、4种WPP结构域相互作用尾锚定蛋白(WIT)、2种WPP蛋白和1种Ran GTP酶激活蛋白(RanGAP)。在本氏烟草瞬时表达后,TaSUN2、TaRanGAP2、TaWIT1和TaWIP1被鉴定为核膜蛋白,而TaWPP1和TaWPP2在细胞核和细胞膜中均有表达。RT-qPCR分析表明,TaSUN2、TaRanGAP2和TaWPP1的转录在真菌感染时强烈上调。此外,使用双分子荧光互补、荧光素酶互补和基于核与分裂泛素的膜酵母双杂交系统,我们证实了TaSUN2与TaWIP1之间以及TaWIP1/WIT1与TaWPP1/WPP2之间的相互作用。小麦叶片中TaSUN2、TaRanGAP2和TaWPP1的沉默促进了白粉病感染和菌丝生长,并降低了TaBRI1、TaBAK1和Ta14-3-3的表达,表明这些核膜蛋白在抗真菌胁迫中发挥积极作用。我们的研究揭示了核膜蛋白的特征,并初步构建了小麦中的SUN-WIP-WPP-RanGAP复合体,这为未来详细阐明它们在小麦中的功能奠定了基础。