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The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis1[w]

机译:对flg22的转录先天免疫反应。相互作用和重叠与Avr基因依赖性防御反应和细菌发病机理[1]

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摘要

Animals and plants carry recognition systems to sense bacterial flagellin. Flagellin perception in Arabidopsis involves FLS2, a Leu-rich-repeat receptor kinase. We surveyed the early transcriptional response of Arabidopsis cell cultures and seedlings within 60 min of treatment with flg22, a peptide corresponding to the most conserved domain of flagellin. Using Affymetrix microarrays, approximately 3.0% of 8,200 genes displayed transcript level changes in flg22 elicited suspension cultures and seedlings. FLARE (Flagellin Rapidly Elicited) genes mostly encode signaling components, such as transcription factors, protein kinases/phosphatases, and proteins that regulate protein turnover. Approximately 80% of flg22-induced genes were also up-regulated in Arabidopsis seedlings treated with cycloheximide. This suggests that many FLARE genes are negatively regulated by rapidly turned-over repressor proteins. Twenty-one tobacco Avr9/Cf-9 rapidly elicited (ACRE) cDNA full-length sequences were used to search for their Arabidopsis orthologs (AtACRE). We identified either single or multiple putative orthologs for 17 ACRE genes. For 13 of these ACRE genes, at least one Arabidopsis ortholog was induced in flg22-elicited Arabidopsis suspension cells and seedlings. This result revealed a substantial overlap between the Arabidopsis flg22 response and the tobacco Avr9 race-specific defense response. We also compared FLARE gene sets and genes induced in basal or gene-for-gene interactions upon different Pseudomonas syringae treatments, and infer that Pseudomonas syringae pv tomato represses the flagellin-initiated defense response.
机译:动植物带有识别系统以感知细菌鞭毛蛋白。拟南芥中的鞭毛蛋白感知涉及FLS2,一种富亮重复序列的受体激酶。我们调查了flg22处理后60分钟内拟南芥细胞培养物和幼苗的早期转录反应,flg22是对应于鞭毛蛋白最保守结构域的肽。使用Affymetrix微阵列,在flg22引起的悬浮培养和幼苗中,约有8,200个基因的3.0%显示了转录水平的变化。 FLARE(Flagellin快速淘汰)基因主要编码信号传导成分,例如转录因子,蛋白激酶/磷酸酶和调节蛋白质更新的蛋白质。在用环己酰亚胺处理的拟南芥幼苗中,大约有80%的flg22诱导基因也被上调。这表明许多FLARE基因受到快速翻转的阻遏蛋白的负调控。使用二十一种烟草Avr9 / Cf-9快速引诱(ACRE)cDNA全长序列搜索其拟南芥直系同源基因(AtACRE)。我们确定了17个ACRE基因的单个或多个假定直系同源物。对于这些ACRE基因中的13个,在flg22引发的拟南芥悬浮细胞和幼苗中诱导了至少一个拟南芥直系同源物。该结果揭示了拟南芥flg22应答和烟草Avr9种族特异性防御​​应答之间的实质性重叠。我们还比较了FLARE基因集和在不同丁香假单胞菌治疗后基础或基因对基因相互作用中诱导的基因,并推断丁香假单胞菌PV番茄抑制鞭毛蛋白启动的防御反应。

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