i质粒与植物基因组的相互作用.ppt

Ti-质粒与植物基因组的相互作用 蒋舜媛 董霞 任昶 2002-10-08 DNA重排研究进展专题 What is Ti-plasmid? Ti-plasmid, （short for tumor-inducing plasmid）is a large (150200 kb) double- stranded circular DNA plasmid in a soil bacterium called Agrobacterium tumefaciens, which causes what is known as produces uncontrolled growths (tumors, or galls), normally at the base (crown) of the plant. Ti- plasmid is the key to this tumor production. Figure 1. In the process of causing crown gall Figure 1. In the process of causing crown gall disease, the bacterium disease, the bacterium AgrobacteriumAgrobacterium tumefacienstumefaciens inserts a part of its Ti plasmida region called inserts a part of its Ti plasmida region called T-DNAinto a chromosome of the host plant.T-DNAinto a chromosome of the host plant. Figure 2. Simplified representation of the major regions of the Ti plasmid of A. tumefaciens. The T-DNA, when inserted into the chromosomal DNA of the host plant, directs the synthesis of nopaline, which is then utilized by the bacterium for its own purposes. T-DNA also directs the plant cell to divide in an uncontrolled manner, producing a tumor. Structure of Ti-plasmid T-DNA区 毒性区 (Vir-region, vir) 质粒复制起点 (Origin of replication, ori) 质粒结合转移位点 (Transfer function site, tra) 冠瘿碱分解位点 (ocs or nos) Two types of Ti-plasmid OCS plasmid (octopine ) npTiAch5, pTiA6NC, pTiB653, pTiAg162 NOS plasmid (nopaline ) npTiT37, pTiT38 土壤农杆菌-植物DNA转移体系步骤 植物敏感细胞和土壤农杆菌相互作用 土壤农杆菌的毒性区基因被激活 T-DNA的切割和T复合物生成 T复合物由土壤农杆菌经植物细胞膜 进入植物细胞 T-DNA整合到植物染色体上 Figure 1. In the process of causing crown gall Figure 1. In the process of causing crown gall disease, the bacterium disease, the bacterium AgrobacteriumAgrobacterium tumefacienstumefaciens inserts a part of its Ti plasmida region called inserts a part of its Ti plasmida region called T-DNAinto a chromosome of the host plant.T-DNAinto a chromosome of the host plant. Interaction of Agrobacterium Ti-plasmid DNA and plant cells 植物敏感细胞和土壤农杆菌相互作用 植物受伤产生大量对土壤农杆菌感染敏 感的细胞 n受伤细胞产生一些低分子量的酚类物 质可明显刺激土壤农杆菌Ti质粒上毒性区 表达 n乙酰丁香酮（AS），-羟基乙酰丁香 酮 Ti质粒毒性区基因激活及 T-DNA复合物生成 Insert picture Integration of T-DNA into the chromosome of host plant T-DNA整合到植物染色体上 首先在植物靶DNA上出现一个缺刻(nick) 随着DNA解链，宿主细胞的53外切酶活性使缺刻 扩大成裂口(gap) T-DNA侵入裂口，末端与靶DNA单链上的少数核苷酸 配对形成异源二倍体； T-DNA悬挂在外侧的末端被切割除去，T-DNA与靶 DNA末端相连； 靶DNA上链出现缺刻，以整合后的T-DNA下链为模板 合成T-DNA的第二条链，完成整合过程。 References via NCBI The interaction of Agrobacterium Ti-plasmid DNA and plant cells (1980) Transgene integration in aspen: structures of integration sites and mechanism of T-DNA integration. (2002) How does the T-DNA of Agrobacterium tumefaciens find its way into the plant cell nucleus? (1993) T-DNA integration: a mode of illegitimate recombination in plants. (1991) Transfer and Integration of T-DNA without Cell Injury in the Host Plant. (1997) Integration of Agrobacterium T-DNA into a tobacco chromosome: possible involvement of DNA homology between T-DNA and plant DNA. (1990) Illegitimate recombination in plants: a model for T-DNA integration. (1991) DNA rearrangement associated with the integration of T-DNA in tobacco: an example for multiple duplications of DNA around the integration target. (1995) The DNA sequences of T-DNA junctions suggest that complex T-DNA loci are formed by a recombination process resembling T-DNA integration. (1999) Two different but related mechanisms are used in plants for the repair of genomic double-strand breaks by homologous recombination. (1996) Production of transgenic plants with recombinant Ti- plasmid Formation of Cointegrate Ti- plasmid Generation of a transgenetic plant via the growth of a cell transformed by T-DNA Figure 3. (a) To produce transgenic plants, an intermediate vector of manageable size is used to clone the segment of interest. In the method shown here, the intermediate vector is then recombined with an attenuated (“disarmed”) Ti plasmid to generate a cointegrate structure bearing the insert of interest and a selectable plant kanamycin-resistance marker between the T -DNA borders, which is all the T-DNA that is necessary to promote insertion. (b) The generation of a transgenic plant through the growth of a cell transformed by T-DNA. Formation of Cointegrate Ti-plasmid Attenuate the natural Ti-plasmid. nhave the entire right-hand region of its T- DNA, including tumor genes and nopaline- synthesis genes deleted, rendering it incapable of tumor formation. Prepare a intermediate vector. Incorporate the intermediate vector. Fig 3.(a) To produce transgenic plants, an intermediate vector of manageable size is used to clone the segment of interest. In the method shown here, the intermediate vector is then recombined with an attenuated (“disarmed”) Ti plasmid to generate a cointegrate structure bearing the insert of interest and a selectable plant kanamycin-resistance marker between the T-DNA borders, which is all the T-DNA that is necessary to promote insertion. Generation of a transgenetic plant via the growth of a cell transformed by T-DNA Bacterial infection transformed plant cell Cell culturation callus Inducing the differentiation of shoots and roots, and transferring to soil transgenetic plant Fig.3 (b) The generation of a transgenic plant through the growth of a cell transformed by T-DNA. infectio n Figure 4. T-DNA and any DNA contained within it are inserted into a plant chromosome in the transgenic plant and then transmitted in a Mendelian