iTRAQ-based protein profiling and functional identification of four genes involved in rice basal resistance against Magnaporthe oryzae in two contrasting rice genotypes.

Chenchen Li, Ziqiang Chen, Yun Deng, Shuyu Jiang, Yan Su, Shaohua Yang, Yan Lin, Dagang Tian
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Abstract

Rice blast, caused by Magnaporthe oryzae, is one of the most destructive rice diseases. Developing blast-resistant rice cultivars represents the most economical and environmentally friend strategy for managing the disease. In our previous study, an isobaric tags for relative and absolute quantitation (iTRAQ)-based comparative protein quantification was carried out to investigate the resistance gene Piz-t gene-mediated resistance response to infection in two contrasting rice genotypes of the Piz-t transgenic Nipponbare line (NPB-Piz-t) and its wild-type Nipponbare (NPB). Here, from the comparisons of differentially expressed proteins (DEPs) of NPB-Piz-t to the avirulent isolate KJ201 (KJ201-Piz-t)and the virulent isolate RB22 (RB22-Piz-t) with mock-treated NPB-Piz-t (Mock-Piz-t), NPB to the virulent isolate KJ201(KJ201-NPB) and RB22 (RB22-NPB) with mock-treated NPB (Mock-NPB), 1, 1, and 6 common DEPs were, respectively, identified at 24, 48 and 72 h post-inoculation (hpi) in the susceptible comparisons of RB22-Pizt/Mock-Piz-t, KJ201-NPB/Mock-NPB, and RB22-NPB/Mock-NPB, involving in gi|54,290,836 and gi|59,800,021 were identified in the resistance comparison KJ201-Piz-t/Mock-Piz-t at 48 and 72 hpi respectively. Moreover, four genes of Os01g0138900 (gi|54,290,836), Os04g0659300 (gi|59,800,021), Os09g0315700 (gi|125,563,186) or Os04g0394200 (gi|21,740,743) were knocked out or overexpressed in NPB using gene over-expression and CRISPR/Cas9 technology, and results verified that the Os01g0138900 obviously affected the rice blast resistance. Further, expression and targeted metabolomics analysis illuminated the resistance response of cysteine-containing substances as gi|59,800,021 under blast infection. These results provide new targets for basal resistance gene identification and open avenues for developing novel rice blast resistant materials.

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基于itraq的水稻对稻瘟病基础抗性相关基因的蛋白谱分析和功能鉴定
稻瘟病是水稻最具破坏性的病害之一,由稻瘟病菌(Magnaporthe oryzae)引起。培育抗稻瘟病品种是防治稻瘟病最经济、最环保的策略。本研究采用等压标签相对绝对定量(iTRAQ)技术,比较了抗性基因pizza -t基因介导的抗侵染应答,研究了pizza -t转基因日本株系(NPB- pizza -t)和野生型日本株系(NPB)的抗性反应。本研究通过比较NPB- pizt与无毒分离物KJ201(KJ201- pizt)、毒力分离物RB22 (RB22- pizt)与模拟处理过的NPB- pizt (mock- pizt)、NPB与毒力分离物KJ201(KJ201-NPB)、RB22 (RB22-NPB)与模拟处理过的NPB (Mock-NPB)的差异表达蛋白(DEPs),分别在接种后24、48和72 h (hpi)在RB22- pizt / mock- pizt、KJ201-NPB/Mock-NPB易感对照中鉴定出1、1和6个常见DEPs。抗性比较kj201 - pizza -t/ mock - pizza -t分别在48和72 hpi时鉴定出RB22-NPB/Mock-NPB参与gi|54,290,836和gi|59,800,021。利用基因过表达和CRISPR/Cas9技术,在NPB中敲除Os01g0138900 (gi|54,290,836)、Os04g0659300 (gi|59,800,021)、Os09g0315700 (gi|125,563,186)和Os04g0394200 (gi|21,740,743) 4个基因,结果证实Os01g0138900对水稻稻瘟病抗性有明显影响。此外,表达和靶向代谢组学分析揭示了含有半胱氨酸的物质gi|59,800,021在blast感染下的耐药反应。这些结果为基础抗性基因的鉴定提供了新的靶点,为水稻抗稻瘟病新材料的开发开辟了道路。
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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