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丁香假单胞菌番茄致病变种的III型效应蛋白AvrPto和AvrPtoB可促进番茄中乙烯依赖性细胞死亡。

Pseudomonas syringae pv. tomato type III effectors AvrPto and AvrPtoB promote ethylene-dependent cell death in tomato.

作者信息

Cohn Jonathan R, Martin Gregory B

机构信息

Boyce Thompson Institute for Plant Research, Tower Rd, Ithaca, NY 14853-1801, USA.

出版信息

Plant J. 2005 Oct;44(1):139-54. doi: 10.1111/j.1365-313X.2005.02516.x.

Abstract

The type III secretion system (TTSS) of Pseudomonas syringae pv. tomato (Pst) injects into the plant cell effector proteins that play an essential role in the formation of bacterial speck disease. To investigate the molecular roles of TTSS effectors in disease formation, we used a cDNA microarray to analyze the expression of approximately 8600 random tomato genes in response to wild-type Pst strain DC3000 and a mutant lacking a functional TTSS. Many of the differentially expressed genes identified encode proteins associated with hormone response or hormone biosynthesis pathways. Using isogenic mutant strains of DC3000, we monitored host transcriptional changes in response to the TTSS effector proteins AvrPto and AvrPtoB, both of which are important virulence factors on susceptible tomato lines. We found that AvrPto and AvrPtoB induce a set of host genes involved in ethylene biosynthesis and signaling, and in particular they regulate the expression of two genes, LeACO1 and LeACO2, encoding the ethylene-forming enzyme ACC oxidase. Analysis of transgenic tomato lines with diminished ACC oxidase activity revealed that ethylene production by the host is required for the full virulence activity of both AvrPto and AvrPtoB. AvrPto and AvrPtoB therefore appear to promote enhanced disease in tomato leaves, in part, by upregulating genes involved in ethylene production.

摘要

丁香假单胞菌番茄致病变种(Pst)的III型分泌系统(TTSS)将效应蛋白注入植物细胞,这些效应蛋白在细菌性斑点病的形成中起关键作用。为了研究TTSS效应蛋白在疾病形成中的分子作用,我们使用cDNA微阵列分析了约8600个随机番茄基因对野生型Pst菌株DC3000和缺乏功能性TTSS的突变体的响应表达情况。许多鉴定出的差异表达基因编码与激素反应或激素生物合成途径相关的蛋白质。利用DC3000的同基因突变菌株,我们监测了宿主对TTSS效应蛋白AvrPto和AvrPtoB的转录变化,这两种效应蛋白在易感番茄品系上都是重要的致病因子。我们发现AvrPto和AvrPtoB诱导了一组参与乙烯生物合成和信号传导的宿主基因,特别是它们调节了两个编码乙烯形成酶ACC氧化酶的基因LeACO1和LeACO2的表达。对ACC氧化酶活性降低的转基因番茄品系的分析表明,宿主产生的乙烯是AvrPto和AvrPtoB完全致病活性所必需的。因此,AvrPto和AvrPtoB似乎部分通过上调参与乙烯产生的基因来促进番茄叶片中病害的加重。

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