植物抗病基因克隆与功能研究进展

植物抗病基因（R基因）是分子植物病理学和植物基因工程研究的热点之一,R基因的克隆及其在抗病反应中的功能研究为揭示植物抗病机制和有效－控制植物病害奠定了基础,本文介绍了R基因的成功克隆方法和克隆新策略,对R基因编码产物的功能进行了分类分析,并对通过遗传工程途径发展R基因介导的抗病植物新品种进行了展望。     

植物抗病分子机制研究进展

近十年来,植物抗病分子机制研究取得显著进展。综述了植物抗病基因的克隆及其结构分析、病原菌无毒基因及其相关致病因子的克隆与研究、信号传导相关因子的克隆及其结构分析以及植物-病原菌的相互作用研究,重点介绍了以植物特异抗病基因为介导的诱导防卫作用机制(包括抗病基因编码毒素蛋白,进而抑制病原菌的繁殖;显性基因编码病原菌致病性的靶标物;抗病基因表达产物直接引发抗病反应和基因对基因的抗病作用机制等)的研究进展,以期为植物抗病育种提供有益的信息。     

植物抗病分子机制研究进展

近十年来,植物抗病分子机制研究取得显著进展.综述了植物抗病基因的克隆及其结构分析、病原菌无毒基因及其相关致病因子的克隆与研究、信号传导相关因子的克隆及其结构分析以及植物-病原菌的相互作用研究,重点介绍了以植物特异抗病基因为介导的诱导防卫作用机制(包括抗病基因编码毒素蛋白,进而抑制病原菌的繁殖;显性基因编码病原菌致病性的靶标物;抗病基因表达产物直接引发抗病反应和基因对基因的抗病作用机制等)的研究进展,以期为植物抗病育种提供有益的信息.     

植物抗病基因同源序列及其在抗病基因克隆与定位中的应用

近10年来已有20多个植物抗病基因被克隆,测序,这些抗病基因所编码的蛋白中大多含有核苷酸结合位点,富含亮氨酸重复序列,蛋白激酶,亮氨酸拉链结构,跨膜结构域,Toll白介素－1区域等保守结构域。利用这些保守结构域合成PCR引物,已扩增出大量的植物抗病基因同源序列（RGA）。对RGA与抗病基因的关系进行了分析,讨论了RGA在研究抗病基因进化中的作用,指出RGA在抗病基因定位和转基因中具有重要意义。     

小麦NBS类抗病基因同源cDNA序列的克隆与特征分析

根据已克隆植物抗病(R)基因NBS保守结构域设计简并引物,采用RT-PCR和cDNA末端快速扩增技术(RACE),在小麦抗叶锈病近等基因系材料TcLr19中进行抗病同源基因cDNA全长的扩增。获得了1个通读的NBS类抗病同源基因S11A11cDNA序列,该序列全长2923bp,编码878个氨基酸序列。生物信息学分析结果表明,该片段含有NB-ARC保守结构域和多个LRR结构域。聚类分析表明,S11A11编码的蛋白与小麦抗叶锈病基因Lr1编码的蛋白亲缘关系较近,而与Lr10亲缘关系较远。半定量RT-PCR分析表明,该基因在小麦叶片中为低丰度组成型表达。本研究在TcLr19小麦中成功获得了抗病基因同源序列,为最终克隆小麦抗叶锈病目的基因奠定了基础。     

植物PDR蛋白转运机制及功能的研究进展

植物多向耐药性（pleiotropic drug resistance,PDR）基因亚家族是ATP结合盒（ATP-binding cassette,ABC）基因家族的一员,其编码的PDR蛋白通过水解ATP释放能量、引起蛋白构象变化实现物质跨膜转运。PDR蛋白可以转运萜类物质、植物生长素和金属离子以应答外界生物和非生物胁迫。综述植物PDR蛋白结构、转运机制及其功能,为克隆植物PDR基因并深入研究其结构与功能提供基础知识。     

植物早期光诱导蛋白基因研究进展

植物早期光诱导蛋白（ELIP）是核编码的叶绿体蛋白,它属于叶绿素结合蛋白超家族的成员。皿伊基因是一古老的基因,在原核细胞中即已存在。真核生物细胞核中的皿,尸基因最初可能来源于其质体基因组。目前,已从30多种不同植物中克隆到该基因,研究发现它们多属于胁迫诱导基因,其功能可能涉及光保护作用。本文介绍了20多年来皿,尸基因的克隆、生物发生、表达调控和功能方面的研究进展,以期为今后的进一步研究奠定基础。     

植物病原物无毒基因及其功能

植物抗病基因与病原物无毒基因产物间直接或间接相互作用导致产生的基因对基因抗性是植物抗病性的重要形式。无毒基因已在多种植物病原物 ,包括真菌、细菌、病毒和卵菌等中得到克隆。绝大多数已克隆无毒基因之间 ,及其与已知蛋白之间 ,均无显著序列同源性。然而 ,多数已克隆植物抗病基因有较高序列一致性 ,产物往往具有相似的结构域。由序列一致性很高的抗病基因产物与没有明显序列同源性的无毒基因产物相互作用 ,介导产生的过敏性细胞坏死和抗病性 ,在产生速度、强度和组织特异性等方面均可能有显著差异。无毒基因具有双重功能 :在含互补抗病基因植物中表现无毒效应 ,而在不含互补抗病基因植物中显示小种、菌株、致病型、或种特异性毒性效应     

植物脂质转运蛋白的研究进展

高等植物脂质转运蛋白(lipid-transfer proteins,LTP)是一类小分子(约9 ku)的碱性蛋白质,已从多种植物中纯化出了LTP,且编码LTP的cDNA及基因也从不同植物中克隆.LTP能够在生物膜之间转运磷脂,因而认为LTP参与了细胞内生物膜形成.而近期的研究又发现LTP具信号肽,可从细胞内分泌到细胞外,位于细胞壁上,因而又对其在细胞内的转运脂质能力产生疑问.而有证据表明LTP参与了角质与腊质的形成、植物的抗病反应和植物对环境变化（温度、盐、干旱协迫）的适应.     

植物细胞质雄性不育

近年来国内外对植物细胞质雄性不育（cytoplasmic male sterility,CMS）在细胞学、生理生化及分子遗传学等方面的研究又取得了新的进展。特别是对育性恢复基因的定位、克隆的研究已取得一定突破,发现编码含保守PPR（pentatricopeptide repeat）模体蛋白的基因在多种植物中与育性恢复密切相关。     

植物TIR-NB-LRR类型抗病基因各结构域的研究进展

植物抗病反应是一个多基因调控的复杂过程,在这个过程中R基因发挥了非常重要的作用。根据其氨基酸基序组成以及跨膜结构域的不同,R基因可以分为多种类型,其中NBS-LRR类型是植物基因组中最大的基因家族之一。TIR-NB-LRR类型的抗病基因又是NB-LRR类型中的一大类,也是目前抗病基因研究的热点。该文总结了TIR-NB-LRR类型抗病基因各个结构域的功能和相关的研究进展。相关研究表明,TIR结构域主要通过自身或异源的二聚体化介导抗性信号的转导,但也有部分研究表明,该结构域可能参与病原菌的特异性识别。NBS结构域常被认为具有"分子开关"的功能,它可以通过结合ADP或ATP来调节植物抗病蛋白的构象变化,从而调节下游抗病信号的传导。LRR结构域在植物与病原菌互作的过程中可以通过与病原菌的无毒蛋白直接或间接互作来特异识别病原菌。也有研究发现,LRR结构域具有调节信号传导的功能。这些信息将为研究植物抗病机理提供理论依据,也为将来通过基因编辑技术对作物进行定向抗病育种提供思路。     

几丁质酶及其研究进展

本文从几丁质酶的分布、发育调节、可诱导性、分子生物学及抗病基因工程等方面近年来的进展进行了综合论述,并对其进一步的应用提出展望。     

植物抗病基因的进化

植物抗病基因在进化中形成了几种共有的进化形式。植物祖先抗病基因的复制创造了新基因座。基因间和基因内重组导致了变异,也导致了新特异性抗病基因的产生。另外,与特异性识别相关的富含亮氨酸重复区顺应于适应性选择。同样,类转座元件在抗病基因座中的插入加速了抗病基因的进化。随着抗病基因的进化,抗病反应也呈现出多样化,代表着植物与病原物动态进化的不同阶段。     

植物广谱抗病基因工程策略与研究进展

系统获得性抗性（SAP）是植物防御病原微生物侵染的一条有效途径。利用基因工程技术改造其表达特性可以提高植物的抗病性,从活性氧的代谢,抗病基因的利用、过敏反应的诱导和SAR的组成性表达等方面论述了植物广谱抗病基因工程的研究策略。已取得的成就及今后的研究方向。     

Intergeneric transfer and functional expression of the tomato disease resistance gene Pto.

Plant disease resistance loci have been used successfully in breeding programs to transfer traits from resistant germplasm to susceptible plant cultivars. The molecular cloning of plant disease resistance genes now permits the transfer of such traits across species boundaries by genetic transformation of recipient hosts. The tomato disease resistance gene Pto confers resistance to strains of the bacterial pathogen Pseudomonas syringae pv tomato expressing the avirulence gene avrPto. Transformation of Nicotiana benthamiana with Pto results in specific resistance to P. s. pv tabaci strains carrying avrPto. The resistant phenotype is manifested by a strong inhibition of bacterial growth and the ability to exhibit a hypersensitive response. Resistance cosegregates with the Pto gene in transgene selfings and testcrosses. Our results demonstrate the conservation of disease resistance functions across genus boundaries and suggest that the utility of host-specific resistance genes can be extended by intergeneric transfer.     

Antibody-mediated resistance against plant pathogens

Plant diseases have a significant impact on the yield and quality of crops. Many strategies have been developed to combat plant diseases, including the transfer of resistance genes to crops by conventional breeding. However, resistance genes can only be introgressed from sexually-compatible species, so breeders need alternative measures to introduce resistance traits from more distant sources. In this context, genetic engineering provides an opportunity to exploit diverse and novel forms of resistance, e.g. the use of recombinant antibodies targeting plant pathogens. Native antibodies, as a part of the vertebrate adaptive immune system, can bind to foreign antigens and eliminate them from the body. The ectopic expression of antibodies in plants can also interfere with pathogen activity to confer disease resistance. With sufficient knowledge of the pathogen life cycle, it is possible to counter any disease by designing expression constructs so that pathogen-specific antibodies accumulate at high levels in appropriate sub-cellular compartments. Although first developed to tackle plant viruses and still used predominantly for this purpose, antibodies have been targeted against a diverse range of pathogens as well as proteins involved in plant–pathogen interactions. Here we comprehensively review the development and implementation of antibody-mediated disease resistance in plants.     

The Genetic and Molecular Basis of Plant Resistance to Pathogens

Plant pathogens have evolved numerous strategies to obtain nutritive materials from their host,and plants in turn have evolved the preformed physical and chemical barriers as well as sophisticated two-tiered immune system to combat pathogen attacks.Genetically, plant resistance to pathogens can be divided into qualitative and quantitative disease resistance,conditioned by major gene(s) and multiple genes with minor effects,respectively.Qualitative disease resistance has been mostly detected in plant defense against biotrophic pathogens,whereas quantitative disease resistance is involved in defense response to all plant pathogens,from biotrophs,hemibiotrophs to necrotrophs.Plant resistance is achieved through interception of pathogen-derived effectors and elicitation of defense response.In recent years,great progress has been made related to the molecular basis underlying host-pathogen interactions.In this review,we would like to provide an update on genetic and molecular aspects of plant resistance to pathogens.     

植物类病变突变体的诱发与突变机制

植物类病变突变体（lesion mimic mutant,LMM）是在无明显逆境或病原物侵染时,植物自发地形成类似病斑的一类突变体。它涉及到细胞程序性死亡（programmed cell death,PCD）,往往能提高植物的抗病能力。因此,它对于揭示植物抗病反应机制,增加植物的广谱抗性具有重要意义。现就植物类病变突变体的诱发与表型特点、突变基因的分子定位与克隆及类病变表型的形成机制研究进展作一简要综述,以期为植物细胞程序性死亡机制和抗病分子作用机制研究提供有益的信息。     

Phospholipase C: Diverse functions in plant biotic stress resistance and fungal pathogenicity

Phospholipase C (PLC) generates various second messenger molecules and mediates phospholipid hydrolysis. In recent years, the important roles of plant and fungal PLC in disease resistance and pathogenicity, respectively, have been determined. However, the roles of PLC in plants and fungi are unintegrated and relevant literature is disorganized. This makes it difficult for researchers to implement PLC-based strategies to improve disease resistance in plants. In this comprehensive review, we summarize the structure, classification, and phylogeny of the PLCs involved in plant biotic stress resistance and fungal pathogenicity. PLCs can be divided into two groups, nonspecific PLC (NPC) and phosphatidylinositol-specific PLC (PI-PLC), which present marked differences in phylogenetic evolution. The products of PLC genes in fungi play significant roles in physiological activity and pathogenesis, whereas those encoded by plant PLC genes mediate the immune response to fungi. This review provides a perspective for the future control of plant fungal diseases.     

Germplasm Modification and Its Potential for Finding New Sources of Resistance to Diseases

In vitro procedures are playing a major role in plant breeding. Embryo rescue, either through the culture of excised embryos derived from incompatible crosses or by means of ovule culture, has been a standard procedure for the introgression of genes conferring disease resistance into economically important plants. Somatic hybridization (i.e., protoplast fusion) has also been demonstrated to have some potential in obtaining hybrids that result from very wide interspecific and intergeneric crosses. Wide crosses have also been achieved by means of in vitro pollination of excised ovaries or ovules. Tissue culture-induced variability in regenerated plant (i.e., somaclonal variation) appears to be an effective way of obtaining undirected genetic change that can enhance disease resistance and yield and alter the growth habit of crops that are normally propagated vegetatively (e.g., potato) or by seed (e.g., tomato). In the near future, the isolation and sequencing of genes that confer resistance to specific plant pathogens will be possible, and transfer of this information between species will become a reality.