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Lumi-Map,一种实时荧光素酶生物发光筛选与 MutMap 结合的突变体的方法,揭示了参与 PAMP 触发免疫的基因。

Lumi-Map, a Real-Time Luciferase Bioluminescence Screen of Mutants Combined with MutMap, Reveals Genes Involved in PAMP-Triggered Immunity.

机构信息

Iwate Biotechnology Research Center, Kitakami, Japan.

Laboratory of Crop Evolution, Graduate School of Agriculture, Kyoto University, Kyoto, Japan.

出版信息

Mol Plant Microbe Interact. 2020 Dec;33(12):1366-1380. doi: 10.1094/MPMI-05-20-0118-TA. Epub 2020 Oct 26.

Abstract

Plants recognize pathogen-associated molecular patterns (PAMPs) to activate PAMP-triggered immunity (PTI). However, our knowledge of PTI signaling remains limited. In this report, we introduce Lumi-Map, a high-throughput platform for identifying causative single-nucleotide polymorphisms (SNPs) for studying PTI signaling components. In Lumi-Map, a transgenic reporter plant line is produced that contains a firefly () gene driven by a defense gene promoter, which generates luminescence upon PAMP treatment. The line is mutagenized and the mutants with altered luminescence patterns are screened by a high-throughput real-time bioluminescence monitoring system. Selected mutants are subjected to MutMap analysis, a whole-genome sequencing-based method of rapid mutation identification, to identify the causative SNP responsible for the luminescence pattern change. We generated nine transgenic reporter lines expressing the gene fused to multiple promoter sequences of defense-related genes. These lines generate luminescence upon activation of FLAGELLIN-SENSING 2 (FLS2) by flg22, a PAMP derived from bacterial flagellin. We selected the -promoter reporter line to identify mutants in the signaling pathway downstream of . After screening 24,000 ethylmethanesulfonate-induced mutants of the reporter line, we isolated 22 mutants with altered expression upon flg22 treatment (abbreviated as mutants). Although five flg22-insensitive mutants harbored mutations in itself, Lumi-Map revealed three genes not previously associated with PTI. Lumi-Map has the potential to identify novel PAMPs and their receptors as well as signaling components downstream of the receptors.[Formula: see text] Copyright © 2020 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

摘要

植物通过识别病原相关分子模式(PAMPs)来激活 PAMP 触发的免疫(PTI)。然而,我们对 PTI 信号转导的认识仍然有限。在本报告中,我们介绍了 Lumi-Map,这是一种用于鉴定研究 PTI 信号转导组件的致病单核苷酸多态性(SNP)的高通量平台。在 Lumi-Map 中,产生了一种转基因报告植物系,该系含有一个由防御基因启动子驱动的萤火虫()基因,该基因在 PAMP 处理时产生发光。对该系进行诱变,并用高通量实时生物发光监测系统筛选发光模式改变的突变体。选择的突变体进行 MutMap 分析,这是一种基于全基因组测序的快速突变鉴定方法,以鉴定导致发光模式变化的致病 SNP。我们生成了九条表达与防御相关基因的多个启动子序列融合的基因的转基因报告系。这些系在 flg22 激活 FLAGELLIN-SENSING 2(FLS2)时产生发光,flg22 是来自细菌鞭毛的 PAMP。我们选择了 -启动子报告系来鉴定下游信号通路中的突变体。在筛选了该报告系的 24000 个乙基甲磺酸诱导的突变体后,我们分离出了 22 个在 flg22 处理时表达改变的突变体(简称突变体)。尽管五个 flg22 不敏感的突变体自身存在突变,但 Lumi-Map 揭示了三个以前与 PTI 无关的基因。Lumi-Map 有可能鉴定新的 PAMPs 及其受体以及受体下游的信号转导组件。[公式:见文本]版权所有©2020 作者。这是一份在 CC BY-NC-ND 4.0 国际许可下分发的开放获取文章。

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