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Microarray Analysis of the Transcriptome for Bacterial Wilt Resistance in Pepper (Capsicum annuum L.)

机译:辣椒细菌性枯萎病转录组的微阵列分析

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Ralstonia solanacearum causes one of the most common soil-borne vascular diseases of diverse plant species, including many solanaceous crops such as tomato and pepper. The resulting disease, bacterial wilt (BW), is devastating and difficult to control using conventional approaches. The aim of this study was to investigate the differentially expressed genes in pepper root systems in response to infection by R. solanacearum. DNA microarray (Capsicum annuum 135K Microarray v3.0 Gene Expression platform) analyses were performed using a susceptible genotype, a€?Chilboka€?, and a resistant genotype, a€?KC350a€?, at 3 time points (1, 3, and 6 days post inoculation). It has been identified 115 resistance-specific genes (R-response genes) and 109 susceptibility-specific genes (S-response gene), which were up-regulated in 1 genotype, but down-regulated in the other genotype. Gene Ontology (GO) analysis for functional categorization indicated that many R-response genes were related to genes that function in xyloglucan biosynthesis and cell wall organization, while S-response genes were involved in the response to stress and cell death. The expression of genes encoding xyloglucan endotransglycosylase/hydrolase (XTH) and ?2-galactosidase were verified by real-time RT-PCR at an early time point of R. solanacearum infection. The results supported the idea that rapidly induced XTH expression in a€?KC350a€? may play an important role in the restructuring and reinforcement of the cell wall and restrict bacterial movement in xylem vessels. In addition, induced expression of ?2-galactosidase in R. solanacearum-infected a€?Chilboka€? implied that degradation of the cell wall structure in vascular tissues by ?2-galactosidase might be an important factor facilitating R. solanacearum invasion of and movement in susceptible host plants.
机译:青枯雷尔氏菌引起多种植物物种最常见的土壤传播的血管疾病之一,包括许多茄科作物,例如番茄和胡椒。由此产生的疾病,细菌性枯萎(BW)是毁灭性的,并且难以使用常规方法控制。这项研究的目的是调查青枯菌感染后辣椒根系中差异表达的基因。在3个时间点分别使用易感基因型Chilboka和耐药基因型KC350a对DNA微阵列(辣椒135K微阵列v3.0基因表达平台)进行了分析。接种后6天)。已经鉴定出115个抗药性特异性基因(R-应答基因)和109个药敏性特异性基因(S-应答基因),它们在一种基因型中被上调,而在另一种基因型中被下调。对功能分类的基因本体论(GO)分析表明,许多R反应基因与在木葡聚糖生物合成和细胞壁组织中起作用的基因有关,而S反应基因则参与对应激和细胞死亡的反应。在青枯菌感染的早期通过实时RT-PCR验证了编码木葡聚糖内切糖苷酶/水解酶(XTH)和β2-半乳糖苷酶的基因的表达。结果支持了在KC350a中快速诱导XTH表达的想法。可能在细胞壁的重组和增强中起重要作用,并限制木质部血管中的细菌运动。另外,诱导的β2-半乳糖苷酶在青枯病菌感染的Chilboka中表达。暗示β2-半乳糖苷酶降解血管组织中的细胞壁结构可能是促进茄形红杆菌入侵易感宿主植物并在其中迁移的重要因素。

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