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首页> 外文期刊>Molecular Microbiology >Involvement of Rad52 in T-DNA circle formation during Agrobacterium tumefaciens-mediated transformation of Saccharomyces cerevisiae
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Involvement of Rad52 in T-DNA circle formation during Agrobacterium tumefaciens-mediated transformation of Saccharomyces cerevisiae

机译:根癌农杆菌介导的啤酒酵母转化过程中Rad52参与T-DNA环的形成。

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摘要

Summary: Agrobacterium tumefaciens cells carrying a tumour inducing plasmid (Ti-plasmid) can transfer a defined region of transfer DNA (T-DNA) to plant cells as well as to yeast. This process of Agrobacterium-mediated transformation (AMT) eventually results in the incorporation of the T-DNA in the genomic DNA of the recipient cells. All available evidence indicates that T-strand transfer closely resembles conjugal DNA transfer as found between Gram-negative bacteria. However, where conjugal plasmid DNA transfer starts via relaxase-mediated processing of a single origin of transfer (oriT), the T-DNA is flanked by two imperfect direct border repeats which are both substrates for the Ti-plasmid encoded relaxase VirD2. Yeast was used as a model system to investigate the requirements of the recipient cell for the formation of T-DNA circles after AMT. It was found that, despite the absence of self-homology on the T-DNA, the homologous repair proteins Rad52 and Rad51 are involved in T-DNA circle formation. A model is presented involving the formation of T-DNA concatemers derived from T-strands by a process of strand-transfer catalysed by VirD2. These concatemers are then resolved into T-DNA circles by homologous recombination in the recipient cell.
机译:简介:携带肿瘤诱导质粒(Ti-质粒)的根癌农杆菌细胞可以将转移DNA(T-DNA)的确定区域转移到植物细胞以及酵母中。农杆菌介导的转化(AMT)过程最终导致T-DNA掺入受体细胞的基因组DNA中。所有现有证据表明,T链转移与革兰氏阴性细菌之间的结合DNA转移非常相似。但是,在通过松弛酶介导的单一转移起点(oriT)进行接合质粒DNA转移的情况下,T-DNA的两侧是两个不完整的直接边界重复序列,这两个序列都是Ti质粒编码的松弛酶VirD2的底物。酵母用作模型系统,以研究AMT后受体细胞对T-DNA环形成的需求。已经发现,尽管在T-DNA上不存在自身同源性,但是同源修复蛋白Rad52和Rad51参与了T-DNA环的形成。提出了一种模型,该模型涉及通过VirD2催化的链转移过程,形成源自T链的T-DNA连接体。然后通过受体细胞中的同源重组将这些串联体分解为T-DNA环。

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