Identification of nuclear membrane SUN proteins and components associated with wheat fungal stress responses.

Huan Guo, Jianfeng Wang, Di Yao, Ligang Yu, Wenting Jiang, Lincai Xie, Shikai Lv, Xiangyu Zhang, Yajuan Wang, Changyou Wang, Wanquan Ji, Hong Zhang
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Abstract

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.

鉴定与小麦真菌胁迫反应相关的核膜 SUN 蛋白和成分。
在真核生物中,包裹基因组 DNA 的核膜由核内膜(INM)、核外膜(ONM)和核周空间组成。位于 INM 中的 SUN 蛋白和 ONM 中的 KASH 蛋白构成了 SUN-KASH NM 桥,发挥着核细胞质复合体交界处的作用。在小麦对真菌胁迫的反应中,含有 SUN 结构域的蛋白质与差异积累蛋白(DAPs)的相关性最高。为了解 SUN 及其相关蛋白在小麦响应病原胁迫中的特性,我们根据其保守基序,对真菌感染下 DAPs 中的 SUN 和 KASH 相关蛋白进行了研究和综合分析。共鉴定出4个SUN蛋白、1个WPP结构域互作蛋白(WIP)、4个WPP结构域互作尾锚蛋白(WIT)、2个WPP蛋白和1个Ran GTP酶激活蛋白(RanGAP)。在烟草中瞬时表达后,TaSUN2、TaRanGAP2、TaWIT1 和 TaWIP1 被鉴定为核膜蛋白,而 TaWPP1 和 TaWPP2 则同时在细胞核和细胞膜中表达。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,我们还利用双分子荧光互补、荧光素酶互补以及基于核和分裂泛素的膜酵母双杂交系统,证实了 TaSUN2 与 TaWIP1 以及 TaWIP1/WIT1 与 TaWPP1/WPP2 之间的相互作用。沉默小麦叶片中的TaSUN2、TaRanGAP2和TaWPP1可促进白粉病感染和菌丝生长,并降低TaBRI1、TaBAK1和Ta14-3-3的表达,表明这些NM蛋白在抗真菌胁迫中发挥了积极作用。我们的研究揭示了NM蛋白的特征,并初步构建了小麦中的SUN-WIP-WPP-RanGAP复合体,为今后详细阐明它们在小麦中的功能奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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