Tedman-Jones Jennifer D, Lei Rita, Jay Florence, Fabro Georgina, Li Xuemei, Reiter Wolf-Dieter, Brearley Charles, Jones Jonathan D G
Sainsbury Laboratory, John Innes Centre, Colney Lane, Norwich, Norfolk NR47UH, UK.
Plant J. 2008 Dec;56(5):691-703. doi: 10.1111/j.1365-313X.2008.03636.x. Epub 2008 Jul 23.
A screen was established for mutants in which the plant defence response is de-repressed. The pathogen-inducible isochorismate synthase (ICS1) promoter was fused to firefly luciferase (luc) and a homozygous transgenic line generated in which the ICS1:luc fusion is co-regulated with ICS1. This line was mutagenized and M(2) seedlings screened for constitutive ICS1:luc expression (cie). The cie mutants fall into distinct phenotypic classes based on tissue-specific localization of luciferase activity. One mutant, cie1, that shows constitutive luciferase activity specifically in petioles, was chosen for further analysis. In addition to ICS1, PR and other defence-related genes are constitutively expressed in cie1 plants. The cie1 mutant is also characterized by an increased production of conjugated salicylic acid and reactive oxygen intermediates, as well as spontaneous lesion formation, all confined to petiole tissue. Significantly, defences activated in cie1 are sufficient to prevent infection by a virulent isolate of Hyaloperonospora parasitica, and this enhanced resistance response protects petiole tissue alone. Furthermore, cie1-mediated resistance, along with PR gene expression, is abolished in a sid2-1 mutant background, consistent with a requirement for salicylic acid. A positional cloning approach was used to identify cie1, which carries two point mutations in a gene required for cell wall biosynthesis and actin organization, MUR3. A mur3 knockout mutant also resists infection by H. parasitica in its petioles and this phenotype is complemented by transformation with wild-type MUR3. We propose that perturbed cell wall biosynthesis may activate plant defence and provide a rationale for the cie1 and the mur3 knockout phenotypes.
建立了一个针对植物防御反应去抑制突变体的筛选体系。将病原体诱导的异分支酸合酶(ICS1)启动子与萤火虫荧光素酶(luc)融合,并构建了一个纯合转基因系,其中ICS1:luc融合基因与ICS1共同调控。对该系进行诱变处理,并筛选M(2)代幼苗中组成型ICS1:luc表达(cie)的植株。根据荧光素酶活性的组织特异性定位,cie突变体可分为不同的表型类别。选择了一个在叶柄中特异性表现出组成型荧光素酶活性的突变体cie1进行进一步分析。除了ICS1,PR基因和其他防御相关基因在cie1植株中也组成型表达。cie1突变体的特征还包括结合态水杨酸和活性氧中间体产量增加,以及自发损伤形成,所有这些都局限于叶柄组织。值得注意的是,cie1中激活的防御足以防止寄生霜霉的强毒株感染,并且这种增强的抗性反应仅保护叶柄组织。此外,在sid2-1突变体背景下,cie1介导的抗性以及PR基因表达被消除,这与水杨酸的需求一致。采用定位克隆方法鉴定出cie1,它在细胞壁生物合成和肌动蛋白组织所需的一个基因MUR3中携带两个点突变。一个mur3敲除突变体在其叶柄中也能抵抗寄生霜霉的感染,并且这种表型通过野生型MUR3转化得以互补。我们提出,细胞壁生物合成的扰动可能激活植物防御,并为cie1和mur3敲除表型提供了理论依据。