Hydrogen sulfide promotes wheat immunity against stripe rust through TaATG6c persulfidation.

IF 6.4
Ying Ma, Fangfang Peng, Ran Zhao, YuPing Li, Jiayu Qian, Yizhe Wang, Guozhi Sun, Jiayu Meng, Jisheng Li, Zhensheng Kang, Xiaojing Wang
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Abstract

Hydrogen sulfide (H2S) is a key gaseous signaling molecule involved in plant growth and stress responses, yet its role in wheat resistance to stripe rust remains poorly understood. Here, we show that exogenous H2S enhances resistance of wheat (Triticum aestivum L.) to Puccinia striiformis f. sp. tritici (Pst), the causative agent of stripe rust. Comparative persulfidation proteomics identified the autophagy-related protein TaATG6c as a Pst-responsive H₂S target. Site-specific mass spectrometry and a modified biotin-switch assay demonstrated that Cys177 and Cys180 of TaATG6c undergo H₂S-induced persulfidation. Structural modeling based on AlphaFold predicted that these two site mutations reduced the binding activity of ATG6c to ATG14. Functional characterization using virus-induced gene silencing (VIGS) revealed that TaATG6 positively regulates wheat immunity against Pst, as silencing TaATG6 promoted fungal growth. Moreover, TaATG6 expression was markedly induced during Pst infection. Notably, the resistance-promoting effect of NaHS was compromised in TaATG6-silenced plants. Conversely, transient overexpression of TaATG6 enhanced wheat resistance to stripe rust, whereas mutation of Cys177 and Cys180 attenuated this effect. Endogenous biotin-switch assays further showed that TaATG6c persulfidation exhibits pathogen-responsive and dynamic characteristics, which were abolished in the TaATG6C177A/C180A mutant. Consistently, H₂S treatment and Pst infection stimulated the accumulation of lipidated ATG8 (ATG8-PE), indicating activation of autophagy, while this response was largely abolished in TaATG6-silenced plants. Together, these results suggest that H₂S promotes autophagy initiation through persulfidation of TaATG6c, thereby enhancing wheat resistance to stripe rust and highlighting a redox-regulated mechanism underlying plant stress adaptation.

硫化氢通过TaATG6c过硫化促进小麦对条锈病的免疫。
硫化氢(H2S)是一种参与植物生长和胁迫反应的关键气体信号分子,但其在小麦抗条锈病中的作用尚不清楚。本研究表明,外源H2S增强了小麦(Triticum aestivum L.)对条锈病病原菌——striiformis f. sp. tritici (Pst)的抗性。比较过硫化蛋白质组学鉴定了自噬相关蛋白TaATG6c作为反应后的H₂S靶标。位点特异性质谱分析和改进的生物素开关分析表明,TaATG6c的Cys177和Cys180经历了h2s诱导的过硫化。基于AlphaFold的结构建模预测,这两个位点突变降低了ATG6c与ATG14的结合活性。利用病毒诱导的基因沉默(VIGS)进行功能鉴定发现,TaATG6正调控小麦对Pst的免疫,因为沉默TaATG6促进了真菌的生长。此外,在Pst感染过程中,TaATG6的表达被显著诱导。值得注意的是,在taatg6沉默的植物中,NaHS的抗性促进作用被削弱。相反,瞬时过表达TaATG6增强了小麦对条锈病的抗性,而突变的Cys177和Cys180则减弱了这一作用。内源性生物素开关实验进一步表明,TaATG6c过硫化表现出病原体响应性和动态特性,而这些特性在TaATG6C177A/C180A突变体中被消除。与此一致的是,h2s处理和Pst感染刺激了脂化ATG8 (ATG8- pe)的积累,表明自噬激活,而在taatg6沉默的植物中,这种反应在很大程度上被消除。综上所述,这些结果表明h2s通过TaATG6c的过硫化促进自噬的启动,从而增强小麦对条锈病的抗性,并强调了植物逆境适应的氧化还原调节机制。
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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