首页> 外文OA文献 >Nucleotide sequence of the insertion sequence found in the T-DNA region of mutant Ti plasmid pTiA66 and distribution of its homologues in octopine Ti plasmid.
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Nucleotide sequence of the insertion sequence found in the T-DNA region of mutant Ti plasmid pTiA66 and distribution of its homologues in octopine Ti plasmid.

机译:在突变体Ti质粒pTiA66的T-DNA区域中发现的插入序列的核苷酸序列,以及其同源物在章鱼碱Ti质粒中的分布。

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摘要

The octopine tumor-inducing (Ti) plasmid pTiA66 has an insertion mutation in its T region (the DNA region incorporated into the plant genome) that results in the slow growth of crown gall tumors. These tumors exhibit hormonal autonomy different from that of the crown gall tumors caused by wild-type Ti plasmids. In the present study, the nucleotide sequences of both the DNA segment inserted into pTiA66 and its target site have been determined. The inserted segment is 2548 base pairs long and has 20-base-pair terminal inverted repeats. An 8-base-pair sequence at the target site is duplicated at both integration junctions. These structural features of the insert suggest that it is a bacterial insertion sequence (IS) element, which we have named IS66. Blot-hybridization analyses using IS66 probes revealed that genomes of octopine Ti plasmids contain at least three sequences homologous to IS66: two homologues are located in the virulence region and one is located between the left-hand (TL-DNA) and right-hand (TR-DNA) portions of T-DNA. The chromosome of Agrobacterium tumefaciens A66 also contains two sequences highly homologous to IS66. These results suggest that the mutant pTiA66 plasmid was generated by translocation of one of the sequences showing homology with IS66 into the T region. The fact that a sequence homologous to IS66 is present between TL-DNA and TR-DNA also suggests that the octopine T region was split into two portions, TL-DNA and TR-DNA, by translocation of IS66 or its relatives. Thus, IS66 may cause genetic and structural variations of the T region and the vir region of the octopine Ti plasmids.
机译:章鱼肿瘤诱导(Ti)质粒pTiA66在其T区(掺入植物基因组的DNA区)具有插入突变,导致冠状胆囊肿瘤缓慢生长。这些肿瘤表现出与野生型Ti质粒引起的冠状胆囊肿瘤不同的激素自主性。在本研究中,已经确定了插入pTiA66的DNA片段及其靶位点的核苷酸序列。插入的片段长2548个碱基对,并具有20个碱基对的末端反向重复序列。在靶位点的8碱基对序列在两个整合连接处重复。插入片段的这些结构特征表明它是细菌插入序列(IS)元素,我们将其命名为IS66。使用IS66探针进行的印迹杂交分析表明,章鱼碱Ti质粒的基因组至少包含与IS66同源的三个序列:两个同源物位于毒力区,一个同源物位于左侧(TL-DNA)和右侧(TL-DNA)之间。 T-DNA)。根癌土壤杆菌A66的染色体也包含两个与IS66高度同源的序列。这些结果表明,突变pTiA66质粒是通过将与IS66同源的序列之一易位到T区而产生的。在TL-DNA和TR-DNA之间存在与IS66同源的序列的事实也表明,通过IS66或其亲代的易位,章鱼碱T区被分成两部分,TL-DNA和TR-DNA。因此,IS66可能引起章鱼碱Ti质粒的T区和vir区的遗传和结构变异。

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