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通过同时破坏水稻多个感病基因中可变 TALE 结合元件来工程广谱细菌性条斑病抗性。

Engineering Broad-Spectrum Bacterial Blight Resistance by Simultaneously Disrupting Variable TALE-Binding Elements of Multiple Susceptibility Genes in Rice.

机构信息

School of Agriculture and Biology/State Key Laboratory of Microbial Metabolism, Shanghai Jiao Tong University, Shanghai 200240, China.

School of Agriculture and Biology/State Key Laboratory of Microbial Metabolism, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Mol Plant. 2019 Nov 4;12(11):1434-1446. doi: 10.1016/j.molp.2019.08.006. Epub 2019 Sep 4.

Abstract

Xanthomonas oryzae pv. oryzae (Xoo), the causal agent of bacterial blight of rice, employs the transcription activator-like effectors (TALEs) to induce the expression of the OsSWEET family of putative sugar transporter genes, which function in conferring disease susceptibility (S) in rice plants. To engineer broad-spectrum bacterial blight resistance, we used CRISPR/Cas9-mediated gene editing to disrupt the TALE-binding elements (EBEs) of two S genes, OsSWEET11 and OsSWEET14, in rice cv. Kitaake, which harbors the recessive resistance allele of Xa25/OsSWEET13. The engineered rice line MS14K exhibited broad-spectrum resistance to most Xoo strains with a few exceptions, suggesting that the compatible strains may contain new TALEs. We identified two PthXo2-like TALEs, Tal5 and Tal7, as major virulence factors in the compatible Xoo strains LN18 and PXO61, respectively, and found that Xoo encodes at least five types of PthXo2-like effectors. Given that PthXo2/PthXo2.1 target OsSWEET13 for transcriptional activation, the genomes of 3000 rice varieties were analyzed for EBE variationsin the OsSWEET13 promoter, and 10 Xa25-like haplotypes were identified. We found that Tal5 and Tal7 bind slightly different EBE sequences in the OsSWEET13 promoter to activate its expression. CRISPR/Cas9 technology was then used to generate InDels in the EBE of the OsSWEET13 promoter in MS14K to creat a new germplasm with three edited OsSWEET EBEs and broad-spectrum resistance against all Xoo strains tested. Collectively, our findings illustrate how to disarm TALE-S co-evolved loci to generate broad-spectrum resistance through the loss of effector-triggered susceptibility in plants.

摘要

稻黄单胞菌(Xanthomonas oryzae pv. oryzae,Xoo)是水稻细菌性条斑病的病原体,它利用转录激活样效应物(TALEs)诱导假定的糖转运体基因 OsSWEET 家族的表达,该基因在赋予水稻植物对疾病的易感性(S)方面发挥作用。为了工程化广谱细菌性条斑病抗性,我们使用 CRISPR/Cas9 介导的基因编辑来破坏水稻品种 Kitaake 中两个 S 基因(OsSWEET11 和 OsSWEET14)的 TALE 结合元件(EBEs),该品种携带有 Xa25/OsSWEET13 的隐性抗性等位基因。工程化的水稻系 MS14K 对大多数 Xoo 菌株表现出广谱抗性,但有几个例外,这表明相容菌株可能含有新的 TALEs。我们鉴定出两个 PthXo2 样 TALEs(Tal5 和 Tal7),分别是相容 Xoo 菌株 LN18 和 PXO61 中的主要毒力因子,并且发现 Xoo 编码至少五种类型的 PthXo2 样效应物。鉴于 PthXo2/PthXo2.1 靶标 OsSWEET13 进行转录激活,分析了 3000 个水稻品种的基因组,以研究 OsSWEET13 启动子中的 EBE 变异,并鉴定出 10 个 Xa25 样单倍型。我们发现 Tal5 和 Tal7 在 OsSWEET13 启动子中结合略有不同的 EBE 序列以激活其表达。然后,使用 CRISPR/Cas9 技术在 MS14K 的 OsSWEET13 启动子的 EBE 中产生 InDels,以创造一种具有三个编辑的 OsSWEET EBE 和对所有测试的 Xoo 菌株均具有广谱抗性的新种质。总之,我们的研究结果说明了如何通过植物中效应物触发的敏感性丧失来消除 TALE-S 共同进化的基因座,以产生广谱抗性。

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