Peng Wen-Fang, Lv Jian-Wei, Ren Xiao-Ping, Huang Li, Zhao Xin-Yan, Wen Qi-Gen, Jiang Hui-Fang
Oil Crops Research Institute of Chinese Academy of Agricultural Sciences/Key Laboratory for Oil Crop Biology of Ministry of Agriculture, Wuhan 430062, China.
Yi Chuan. 2011 Apr;33(4):389-96. doi: 10.3724/sp.j.1005.2011.00389.
Peanut bacterial wilt (BW) caused by Ralstonia solanacearum is one of the most devastating diseases for peanut production in the world. It is believed that breeding and subsequent planting BW-resistant cultivars of peanut (Arachis hypogaea L.) should represent the most effective and economic means of controlling the disease. To illustrate the molecular mechanism of peanut resistant to BW, a BW-resistant cultivar, 'Yuanza 9102', and a BW-sensitive one, 'Zhonghua 12', were infected with Ralstonia solanacearum and differential expression of the genes related to BW-resistance was analyzed using complementary DNA amplified length polymorphism (cDNA-AFLP) technique. The infected 3-leaflet seedlings were followed for 48 h and root samples were taken at 0, 2, 10, 24 and 48 h after inoculation, respectively. A total of 12596 transcript-derived fragments (TDFs) were amplified with 256 primer combinations, including 709 differential expressed TDFs, which were generated from 119 primer combinations. Ninety-eight TDFs were randomly chosen for DNA sequence analysis. BLASTx analysis of the obtained sequences revealed that 40 TDFs encoded gene products associated with energy, transcription, signal transduction, defense, metabolism, cell growth, cell structure or/and protein synthesis. Analysis of the expression of four genes by qRT-PCR verified the results from cDNA-AFLP. Strikingly, one of the identified TDFs, 32-54-1, occurred for 47 times in a known BW-resistant SSH library. These results suggest that resistance to BW in peanut involves multifaceted biochemical and physiological reactions, including regulation of the genes involved in different pathways, such as defense, singal transduction, metabolism, transcription and abiotic stresses. The TDF 32-54-1 was predicted to be closely related to BW resistance in peanut.
由青枯雷尔氏菌引起的花生青枯病是世界花生生产中最具毁灭性的病害之一。人们认为,培育并随后种植抗青枯病的花生品种应该是控制该病最有效且经济的手段。为阐明花生抗青枯病的分子机制,用青枯雷尔氏菌感染了一个抗青枯病品种‘远杂9102’和一个感病品种‘中花12’,并使用cDNA扩增片段长度多态性(cDNA-AFLP)技术分析了与抗青枯病相关基因的差异表达情况。对接种后的三叶期幼苗进行48小时跟踪观察,并分别在接种后0、2、10、24和48小时采集根系样本。用256对引物组合共扩增出12596个转录本衍生片段(TDF),其中包括由119对引物组合产生的709个差异表达TDF。随机选择98个TDF进行DNA序列分析。对所得序列进行BLASTx分析表明,40个TDF编码的基因产物与能量、转录、信号转导、防御、代谢、细胞生长、细胞结构或/和蛋白质合成相关。通过qRT-PCR对4个基因的表达分析验证了cDNA-AFLP的结果。引人注目的是,在一个已知的抗青枯病SSH文库中,鉴定出的一个TDF(32-54-1)出现了47次。这些结果表明,花生对青枯病的抗性涉及多方面的生化和生理反应,包括参与不同途径的基因调控,如防御、信号转导、代谢、转录和非生物胁迫。预测TDF 32-54-1与花生对青枯病的抗性密切相关。