Transcriptomic analysis of wheat reveals possible resistance mechanism mediated by Yr10 to stripe rust.

Zhongyi Wu, Gaohua Zhang, Ran Zhao, Qi Gao, Jinchen Zhao, Xiaoxu Zhu, Fangyan Wang, Zhensheng Kang, Xiaojing Wang
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Abstract

Stripe rust, caused by Puccinia striiformis f. sp. tritici (Pst), is a catastrophic disease that threatens global wheat yield. Yr10 is a race-specific all-stage disease resistance gene in wheat. However, the resistance mechanism of Yr10 is poorly characterized. Therefore, to elucidate the potential molecular mechanism mediated by Yr10, transcriptomic sequencing was performed at 0, 18, and 48 h post-inoculation (hpi) of compatible wheat Avocet S (AvS) and incompatible near-isogenic line (NIL) AvS + Yr10 inoculated with Pst race CYR32. Respectively, 227, 208, and 4050 differentially expressed genes (DEGs) were identified at 0, 18, and 48 hpi between incompatible and compatible interaction. The response of Yr10 to stripe rust involved various processes and activities, as indicated by the results of Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Specifically, the response included photosynthesis, defense response to fungus, metabolic processes related to salicylic acid (SA) and jasmonic acid (JA), and activities related to reactive oxygen species (ROS). Ten candidate genes were selected for qRT-PCR verification and the results showed that the transcriptomic data was reliable. Through the functional analysis of candidate genes by the virus-induced gene silencing (VIGS) system, it was found that the gene TaHPPD (4-hydroxyphenylpyruvate dioxygenase) negatively regulated the resistance of wheat to stripe rust by affecting SA signaling, pathogenesis-related (PR) gene expression, and ROS clearance. Our study provides insight into Yr10-mediated resistance in wheat.

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小麦转录组分析揭示了Yr10介导的抗条锈病机制。
小麦条锈病是一种严重威胁全球小麦产量的灾难性病害。Yr10是小麦的一个小种特异性全阶段抗病基因。然而,Yr10的电阻机制却没有得到很好的表征。因此,为了阐明Yr10介导的潜在分子机制,在相容小麦Avocet S(AvS)和不相容近等基因系AvS接种后0、18和48小时进行了转录组测序 + Yr10接种Pst小种CYR32。在不相容和相容相互作用之间,分别在0、18和48hpi处鉴定出227、208和4050个差异表达基因(DEG)。基因本体论(GO)富集分析和京都基因与基因组百科全书(KEGG)通路分析结果表明,Yr10对条锈病的反应涉及多种过程和活性。具体而言,反应包括光合作用、对真菌的防御反应、与水杨酸(SA)和茉莉酸(JA)相关的代谢过程,以及与活性氧(ROS)有关的活性。选择10个候选基因进行qRT-PCR验证,结果表明转录组学数据是可靠的。通过病毒诱导基因沉默(VIGS)系统对候选基因的功能分析,发现基因TaHPPD(4-羟基苯基丙酮酸双加氧酶)通过影响SA信号传导、发病机制相关(PR)基因表达和ROS清除,对小麦抗条锈病负调控。我们的研究提供了对Yr10介导的小麦抗性的深入了解。
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