Mould Michael J R, Xu Tao, Barbara Mary, Iscove Norman N, Heath Michèle C
Department of Botany, University of Toronto, 25 Willcocks St., Toronto, Ontario, Canada M5S 3B2.
Mol Plant Microbe Interact. 2003 Sep;16(9):835-45. doi: 10.1094/MPMI.2003.16.9.835.
As the cowpea rust fungus penetrates the wall of a cowpea epidermal cell, resistant and susceptible plants exhibit different ultrastructural and cytochemical changes within the epidermal protoplast. To examine plant gene expression at this stage of infection, cytoplasm was extracted from individual inoculated or uninoculated epidermal cells before the fungal penetration peg reached the cell lumen. Initial differential colony hybridization screening of an expressed sequence tag library constructed from globally amplified cDNAs generated from the inoculated resistant cells resulted in 80 clones (out of 835) with a differential hybridization pattern. Further slot-blot screening and screening of the amplified cDNAs generated from inoculated or uninoculated, resistant or susceptible cells revealed 28 separate genes, mostly with no matching sequences in the databases, that were up-regulated in response to the growth of the fungus through the wall of resistant or susceptible cells. Five genes, including those coding for beta- and alpha-tubulin, were found to be down-regulated specifically in inoculated, susceptible cells, and five were specifically up-regulated in inoculated, resistant cells, including a PR-10 homolog and a phenylalanine ammonia-lyase gene. Probing the amplified cDNAs from each cell type for the expression of cell death-related genes revealed that an LLS1 homolog (vuLLS1), cloned from cowpea, was up-regulated by infection in both resistant and susceptible cells and that a homolog of HSR203J was differentially up-regulated in resistant cells. These data show that changes in gene expression predicting the subsequent expression of susceptibility or hypersensitive resistance to fungal infection occur prior to the fungus entering the cell lumen.
当豇豆锈菌穿透豇豆表皮细胞的细胞壁时,抗性和感病植株的表皮原生质体内会出现不同的超微结构和细胞化学变化。为了检测感染这个阶段的植物基因表达情况,在真菌侵入栓到达细胞腔之前,从单个接种或未接种的表皮细胞中提取细胞质。对由接种的抗性细胞中全局扩增的cDNA构建的表达序列标签文库进行初步差异菌落杂交筛选,结果在835个克隆中有80个克隆呈现差异杂交模式。进一步的狭缝杂交筛选以及对接种或未接种、抗性或感病细胞中扩增的cDNA进行筛选,发现了28个不同的基因,这些基因大多在数据库中没有匹配序列,它们在真菌穿透抗性或感病细胞的细胞壁生长时被上调表达。发现5个基因,包括编码β-微管蛋白和α-微管蛋白的基因,在接种的感病细胞中特异性下调,还有5个基因在接种的抗性细胞中特异性上调,包括一个病程相关蛋白10(PR-10)同源物和一个苯丙氨酸解氨酶基因。对每种细胞类型扩增的cDNA进行细胞死亡相关基因表达的检测,结果显示从豇豆中克隆的一个LLS1同源物(vuLLS1)在抗性和感病细胞中均因感染而上调表达,并且一个HSR203J同源物在抗性细胞中差异上调。这些数据表明,在真菌进入细胞腔之前,就已经发生了预测对真菌感染后续感病性或过敏反应抗性表达的基因表达变化。