Navarro Lionel, Zipfel Cyril, Rowland Owen, Keller Ingo, Robatzek Silke, Boller Thomas, Jones Jonathan D G
The Sainsbury Laboratory, John Innes Centre, Norwich Research Park, United Kingdom.
Plant Physiol. 2004 Jun;135(2):1113-28. doi: 10.1104/pp.103.036749. Epub 2004 Jun 4.
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.
动植物都具有识别系统来感知细菌鞭毛蛋白。拟南芥中对鞭毛蛋白的感知涉及FLS2,一种富含亮氨酸重复序列的受体激酶。我们研究了拟南芥细胞培养物和幼苗在用flg22(一种对应于鞭毛蛋白最保守结构域的肽)处理60分钟内的早期转录反应。使用Affymetrix微阵列,在flg22诱导的悬浮培养物和幼苗中,8200个基因中约3.0%的基因转录水平发生了变化。FLARE(鞭毛蛋白快速诱导)基因大多编码信号成分,如转录因子、蛋白激酶/磷酸酶以及调节蛋白质周转的蛋白质。在用环己酰亚胺处理的拟南芥幼苗中,约80%的flg22诱导基因也被上调。这表明许多FLARE基因受到快速周转的阻遏蛋白的负调控。使用21个烟草Avr9/Cf-9快速诱导(ACRE)cDNA全长序列来搜索它们在拟南芥中的直系同源基因(AtACRE)。我们为17个ACRE基因鉴定出了单个或多个假定的直系同源基因。对于其中13个ACRE基因,至少有一个拟南芥直系同源基因在flg22诱导的拟南芥悬浮细胞和幼苗中被诱导。这一结果揭示了拟南芥flg22反应与烟草Avr9小种特异性防御反应之间存在大量重叠。我们还比较了FLARE基因集以及在不同丁香假单胞菌处理下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番茄致病变种会抑制鞭毛蛋白引发的防御反应。