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赋予质粒不相容性和稳定性增强的pTi-樱花DNA区域的鉴定。

Identification of pTi-SAKURA DNA region conferring enhancement of plasmid incompatibility and stability.

作者信息

Yamamoto Shinji, Uraji Misugi, Tanaka Katsuyuki, Moriguchi Kazuki, Suzuki Katsunori

机构信息

Department of Biological Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, Japan.

出版信息

Genes Genet Syst. 2007 Jun;82(3):197-206. doi: 10.1266/ggs.82.197.

DOI:10.1266/ggs.82.197
PMID:17660690
Abstract

In Agrobacterium tumefaciens, the stability of Ti plasmids differs depending on the strain. So far, little is known about genes that cause the difference in stability. The repABC operon is responsible for replication and incompatibility of Ti plasmids. We constructed recombinant plasmids carrying the repABC operon and different portions of pTi-SAKURA. Cells having the recombinant plasmids that harbored a 2.6-kbp NheI fragment of pTi-SAKURA were found to be transformed via conjugation 100-fold less frequently with a small incompatible repABC plasmid than cells having the recombinant plasmids lacking the 2.6-kbp NheI fragment. Since the phenomenon occurred only when the resident and incoming plasmids belonged to the same incompatibility group, it was suggested that the 2.6-kbp NheI fragment bears the potential enhancing incompatibility. The fragment contained an operon consisting of two open reading frames, tiorf24 and tiorf25. tiorf24 is an orphan gene, whereas tiorf25 is a homologue of a group of plasmid stability genes. Removal of the 2.6-kbp fragment from the resident pTi-SAKURA increased the resident plasmid ejection ratio by the incoming repABC plasmid, whereas addition of the fragment to pTiC58 decreased the ejection ratio, and the loss ratio during growth at 37 degrees C. These data suggest that tiorf24 and tiorf25 are responsible for the stability of pTi-SAKURA, and reduce, in the host bacterium, the frequency of ejection of the resident plasmid, presumably through an incompatibility mechanism.

摘要

在根癌农杆菌中,Ti质粒的稳定性因菌株而异。到目前为止,对于导致稳定性差异的基因了解甚少。repABC操纵子负责Ti质粒的复制和不相容性。我们构建了携带repABC操纵子和pTi-SAKURA不同片段的重组质粒。发现含有携带pTi-SAKURA 2.6-kbp NheI片段的重组质粒的细胞,通过接合被一个小的不相容repABC质粒转化的频率比缺乏2.6-kbp NheI片段的重组质粒的细胞低100倍。由于这种现象仅在常驻质粒和导入质粒属于同一不相容组时才会发生,因此表明2.6-kbp NheI片段具有增强不相容性的潜力。该片段包含一个由两个开放阅读框tiorf24和tiorf25组成的操纵子。tiorf24是一个孤儿基因,而tiorf25是一组质粒稳定性基因的同源物。从常驻pTi-SAKURA中去除2.6-kbp片段会增加导入的repABC质粒导致的常驻质粒排出率,而将该片段添加到pTiC58中则会降低排出率以及在37℃生长期间的丢失率。这些数据表明,tiorf24和tiorf25负责pTi-SAKURA的稳定性,并可能通过不相容机制降低宿主细菌中常驻质粒的排出频率。

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