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在被根癌农杆菌感染的植物中形成复杂的染色体外 T-DNA 结构。

Formation of complex extrachromosomal T-DNA structures in Agrobacterium tumefaciens-infected plants.

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109-1048, USA.

出版信息

Plant Physiol. 2012 Sep;160(1):511-22. doi: 10.1104/pp.112.200212. Epub 2012 Jul 13.

Abstract

Agrobacterium tumefaciens is a unique plant pathogenic bacterium renowned for its ability to transform plants. The integration of transferred DNA (T-DNA) and the formation of complex insertions in the genome of transgenic plants during A. tumefaciens-mediated transformation are still poorly understood. Here, we show that complex extrachromosomal T-DNA structures form in A. tumefaciens-infected plants immediately after infection. Furthermore, these extrachromosomal complex DNA molecules can circularize in planta. We recovered circular T-DNA molecules (T-circles) using a novel plasmid-rescue method. Sequencing analysis of the T-circles revealed patterns similar to the insertion patterns commonly found in transgenic plants. The patterns include illegitimate DNA end joining, T-DNA truncations, T-DNA repeats, binary vector sequences, and other unknown "filler" sequences. Our data suggest that prior to T-DNA integration, a transferred single-stranded T-DNA is converted into a double-stranded form. We propose that termini of linear double-stranded T-DNAs are recognized and repaired by the plant's DNA double-strand break-repair machinery. This can lead to circularization, integration, or the formation of extrachromosomal complex T-DNA structures that subsequently may integrate.

摘要

根癌农杆菌是一种独特的植物病原细菌,以其转化植物的能力而闻名。在根癌农杆菌介导的转化过程中,转移 DNA(T-DNA)的整合和转基因植物基因组中复杂插入的形成仍知之甚少。在这里,我们表明,在感染后,感染根癌农杆菌的植物中会立即形成复杂的染色体外 T-DNA 结构。此外,这些染色体外复杂的 DNA 分子可以在体内环化。我们使用一种新颖的质粒拯救方法回收了环状 T-DNA 分子(T- 环)。对 T- 环的测序分析显示出与在转基因植物中常见的插入模式相似的模式。这些模式包括非特异性 DNA 末端连接、T-DNA 截断、T-DNA 重复、二元载体序列和其他未知的“填充”序列。我们的数据表明,在 T-DNA 整合之前,转移的单链 T-DNA 被转化为双链形式。我们提出,线性双链 T-DNA 的末端被植物的 DNA 双链断裂修复机制识别和修复。这可能导致环状、整合或染色体外复杂 T-DNA 结构的形成,随后可能进行整合。

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