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植物抗病机制是目前研究的热点。在长期的进化过程中,植物形成了一系列复杂有效的防御机制来抵御、破坏病原物的侵染。植物抗病基因在植物抗性反应中起着重要的作用,植物一旦监测到病原物马上起始防御反应,并伴随着植物体内一系列细胞和生理生化的变化。近年来,基因沉默作为一个重要的细胞内防御外源核酸的机制,越来越受到科学家重视。综述了植物抗病基因和基因沉默机制在植物抗病反应中的重要作用,并对研究植物抗病机制的前景做了展望。 相似文献
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水稻白叶枯病抗性基因的研究与分子育种 总被引:24,自引:0,他引:24
由革兰氏阴性菌黄单孢水稻变种(Xanthomonas oryzae pv.oryzae,Xoo)引起的白叶枯病是世界水稻生产中最严重的细菌性病害。白叶枯病是一种维管束病害,自然条件下,病菌通常由水孔或伤口侵入,沿叶脉产生灰白色病斑。田间常在分蘖期观察到病症,并随植株的生长而发展,至抽穗期达到高峰。水稻遭受白叶枯病后,一般减产20%-30%,严重时甚至绝收。白叶枯病最早于1884年在日本福岗地区发现 相似文献
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植物抗病基因的克隆与分子育种翟文学,朱立煌(中国科学院遗传所植物生物技术实验室)植物抗病常常是由于宿主和病原菌的基本遗传因素的不相容引起。这些遗传因素决定了感染早期落特对病原菌的识别,然后导致植物中一系列生化反应、这些反应组成了名为过敏反应(HpersensitiveResponseHR)的区域防御机构,过敏反应特点是病原菌感染部位附近的植物细胞的快速坏死. 相似文献
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植物与病原微生物互作分子基础的研究进展 总被引:4,自引:0,他引:4
植物在与病原微生物共同进化过程中形成了复杂的免疫防卫体系。植物的先天免疫系统可大致分为两个层面。第一个层面的免疫基于细胞表面的模式识别受体对病原物相关分子模式的识别,该免疫过程被称为病原物相关分子模式触发的免疫(PAMP-triggered immunity,PTI),能帮助植物抵抗大部分病原微生物;第二个层面的免疫起始于细胞内部,主要依靠抗病基因编码的蛋白产物直接或间接识别病原微生物分泌的效应子并且激发防卫反应,来抵抗那些能够利用效应子抑制第一层面免疫的病原微生物,这一过程被称为效应子触发的免疫(Effector-triggered immunity,ETI)。这两个层面的免疫都是基于植物对"自我"及"非我"的识别,依靠MAPK级联等信号网络,将识别结果传递到细胞核内,调控相应基因的表达,做出适当的免疫应答。本文着重阐述了植物与病原微生物互作过程中不同层面的免疫反应所发生主要事件的分子基础及研究进展。 相似文献
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《Journal of Plant Interactions》2013,8(1):84-93
Cuscuta is a stem holoparasitic plant without leaves or roots, parasitizing various types of host plants and causing major problems for certain crops. Cuscuta is known as a generalist and, thus, must have unique parasite strategies to cope with different host plants. For elucidating metabolic responses and mechanisms of parasitization, metabolomic approaches using GC/MS were applied. We compared five stages of Cuscuta japonica: early stage seedlings, with far red light (FR) cue, with contact signal, haustorium induced seedlings by both signals and adult plant parasites on host plants. Sugars, amino acids, organic acids, nucleic acids, and polyols were identified from the polar phase fraction. The apical part contained metabolite profiles different from the haustorium induced part or the basal part. Amino acid and some organic acids were up-regulated for haustorium induction but decreased after parasitization. After attachment to different host plants, metabolite profiles of Cuscuta japonica changed dramatically due to the absorption of specific host plant metabolites such as pinitol. Cuscuta seedlings attached to pinitol rich host plants contained more pinitol and showed different profiles from those attached to plants having less or lacking pinitol. 相似文献
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The interaction between waterlogging and salinity in higher plants: causes,consequences and implications 总被引:15,自引:0,他引:15
This paper reviews a range of studies under controlled conditions (glasshouse and growth cabinet) focusing on the effects of the interaction between waterlogging (hypoxia) and salinity on the ion relations, growth and survival of higher plants. The literature shows that in general, waterlogging under saline conditions causes increased Na+ and Cl– concentrations in the shoot, due initially to increased rates of transport. These increased concentrations in the shoots have adverse effects on plant growth and survival. It is argued that the interaction between waterlogging and salinity has major implications for saltland management, and for the selection and breeding of plants adapted to saltland. 相似文献
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益生菌与肠黏膜互作的分子机制研究进展 总被引:1,自引:0,他引:1
益生菌是一类定植于动物肠道,可辅助动物消化功能,维护肠道菌群平衡并可影响肠道免疫系统,有益于动物健康的重要调节性菌群。该类菌群与动物肠上皮细胞间互作的分子机制包括菌体表面分子如磷脂壁酸(phosphatidicacid,LTA)、表面层蛋白(Slayerprotein)等与宿主的粘附相关蛋白分子结合,通过占位效应抑制有害菌群在肠道内的定植;益生菌还可刺激肠道细胞分泌B防御素2、细菌素和有机酸等可抑制甚至杀灭有害菌群;在益生菌作用下,肠道上皮细胞可增强粘液糖蛋白、紧密连接蛋白occludin和ZO-1等分子的表达,加厚并加固肠道黏膜屏障;益生菌相关抗原可通过与抗原递呈细胞表面模式识别受体(TLRs等)分子结合,激活递呈细胞,启动各免疫细胞的交互作用,调节肠道免疫状态。 相似文献
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Steven A. Frank 《Evolutionary ecology》1993,7(1):45-75
Summary The genetic polymorphism maintained by host-pathogen coevolution is analysed in a multilocus model. The model assumes gene-for-gene interactions of the type commonly observed between host plants and their fungal pathogens. Unstable (epidemic) systems maintain more resistance genes, fewer virulence genes, and less overall genetic diversity than stable (endemic) diseases. The stability of the system depends primarily on demographic parameters, such as the pathogen's intrinsic rate of increase, rather than genetic parameters, such as the costs of resistance and virulence. At equilibrium the model predicts that the number of resistance alleles in each host plant follows a binomial distribution that depends on the cost to the pathogen for carrying virulence alleles. Similarly, the number of virulence alleles in each pathogen spore follows a binomial distribution that depends on one minus the cost to the host for carrying resistance alleles. Data from wild populations match the predicted binomial distributions. 相似文献
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F. A. van Eeuwijk A. Mesterhazy Ch. I. Kling P. Ruckenbauer L. Saur H. Bürstmayr M. Lemmens L. C. P. Keizer N. Maurin C. H. A. Snijders 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1995,90(2):221-228
To determine whether resistance to Fusarium head blight in winter wheat is horizontal and non-species specific, 25 genotypes from five European countries were tested at six locations across Europe in the years 1990, 1991, and 1992. The five genotypes from each country had to cover the range from resistant to susceptible. The locations involved were Wageningen, Vienna, Rennes, Hohenheim, Oberer Lindenhof, and Szeged. In total, 17 local strains of Fusarium culmorum, F. graminearum, and F. nivale were used for experimental inoculation. One strain, F. culmorum IPO 39-01, was used at all locations. Best linear unbiased predictions (BLUPs) for the head blight ratings of the genotypes were formed within each particular location for each combination of year and strain. The BLUPs over all locations were collected in a genotype-by environment table in which the genotypic dimension consisted of the 25 genotypes, while the environmental dimension was made up of 59 year-by-strain-by-location combinations. A multiplicative model was fitted to the genotype by-environment interaction in this table. The inverses of the variances of the genotype-by-environment BLUPs were used as weights. Interactions between genotypes and environments were written as sums of products between genotypic scores and environmental scores. After correction for year-by-location influence very little variation in environmental scores could be ascribed to differences between strains. This provided the basis for the conclusion that the resistance to Fusarium head blight in winter wheat was of the horizontal and non-species specific type. There was no indication for any geographical pattern in virulence genes. Any reasonable aggressive strain, a F. culmorum strain for the cool climates and a F. graminearum strain for the warmer humid areas, should be satisfactory for screening purposes. 相似文献