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通过由OsMYB30诱导的增强木质化作用,厚壁组织细胞加厚可防止真菌穿透水稻叶片。

Sclerenchyma cell thickening through enhanced lignification induced by OsMYB30 prevents fungal penetration of rice leaves.

作者信息

Li Weitao, Wang Kang, Chern Mawsheng, Liu Yuchen, Zhu Ziwei, Liu Jiang, Zhu Xiaobo, Yin Junjie, Ran Li, Xiong Jun, He Kaiwei, Xu Liting, He Min, Wang Jing, Liu Jiali, Bi Yu, Qing Hai, Li Mingwu, Hu Kun, Song Li, Wang Long, Qi Tuo, Hou Qingqing, Chen Weilan, Li Yan, Wang Wenming, Chen Xuewei

机构信息

State Key Laboratory of Crop Gene Exploration and Utilisation in Southwest China, State Key Laboratory of Hybrid Rice, Key Laboratory of Major Crop Diseases & Collaborative Innovation Center for Hybrid Rice in Yangtze River Basin, Rice Research Institute, Sichuan Agricultural University at Wenjiang, Chengdu, Sichuan, 611130, China.

Department of Plant Pathology, University of California, Davis, CA, 95616, USA.

出版信息

New Phytol. 2020 Jun;226(6):1850-1863. doi: 10.1111/nph.16505. Epub 2020 Mar 31.

Abstract

Broad-spectrum resistance is highly preferred in crop breeding programmes. Previously, we have reported the identification of the broad-spectrum resistance-Digu 1 (bsr-d1) allele from rice Digu. The bsr-d1 allele prevents activation of Bsr-d1 expression by Magnaporthe oryzae infection and degradation of H O by peroxidases, leading to resistance to M. oryzae. However, it remains unknown whether defence pathways other than H O burst and peroxidases contribute to the bsr-d1-mediated immunity. Blast resistance was determined in rice leaves by spray and punch inoculations. Target genes of OsMYB30 were identified by one-hybrid assays in yeast and electrophoretic mobility shift assay. Lignin content was measured by phloroglucinol-HCl staining, and acetyl bromide and thioacidolysis methods. Here, we report the involvement of the OsMYB30 gene in bsr-d1-mediated blast resistance. Expression of OsMYB30 was induced during M. oryzae infection or when Bsr-d1 was knocked out or downregulated, as occurs in bsr-d1 plants upon infection. We further found that OsMYB30 bound to and activated the promoters of 4-coumarate:coenzyme A ligase genes (Os4CL3 and Os4CL5) resulting in accumulation of lignin subunits G and S. This action led to obvious thickening of sclerenchyma cells near the epidermis, inhibiting M. oryzae penetration at the early stage of infection. Our study revealed novel components required for bsr-d1-mediated resistance and penetration-dependent immunity, and advanced our understanding of broad-spectrum disease resistance.

摘要

广谱抗性在作物育种计划中备受青睐。此前,我们报道了从水稻迪古中鉴定出广谱抗性基因Bsr-d1(bsr-d1)等位基因。bsr-d1等位基因可防止稻瘟病菌感染激活Bsr-d1的表达以及过氧化物酶对H₂O₂的降解,从而导致对稻瘟病菌产生抗性。然而,除了H₂O₂爆发和过氧化物酶之外的防御途径是否有助于bsr-d1介导的免疫反应仍不清楚。通过喷雾接种和打孔接种测定水稻叶片的抗稻瘟病性。通过酵母单杂交试验和电泳迁移率变动分析鉴定了OsMYB30的靶基因。通过间苯三酚-盐酸染色、乙酰溴法和硫代酸解方法测定木质素含量。在此,我们报道了OsMYB30基因参与bsr-d1介导的抗稻瘟病性。在稻瘟病菌感染期间,或者当Bsr-d1被敲除或下调时(如感染时bsr-d1植株中发生的情况),OsMYB30的表达会被诱导。我们进一步发现,OsMYB30与4-香豆酸:辅酶A连接酶基因(Os4CL3和Os4CL5)的启动子结合并激活它们,导致木质素亚基G和S的积累。这一作用导致表皮附近厚壁组织细胞明显增厚,在感染早期抑制稻瘟病菌的侵入。我们的研究揭示了bsr-d1介导的抗性和穿透依赖性免疫所需的新成分,并加深了我们对广谱抗病性的理解。

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