Yamamoto Shinji, Agustina Vita, Sakai Ayako, Moriguchi Kazuki, Suzuki Katsunori
Department of Biological Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, Japan.
Department of Biological Science, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, Japan.
Plasmid. 2017 Mar;90:20-29. doi: 10.1016/j.plasmid.2017.02.003. Epub 2017 Feb 24.
Ti/Ri plasmids in pathogenic Agrobacterium species are repABC replicons that are stably maintained by the function of repABC genes. Two Ti plasmids, pTiBo542 and pTiS4, belonging to incRh2 and incRh4 incompatibility groups, respectively, were reported to carry two repABC loci. In the present study, to reveal the roles of the two repABC loci in the two plasmids, we constructed mini-replicons carrying any one or both of the repABC loci (referred to as repABC1 and repABC2 here) and examined their replication and incompatibility properties. The introduction of mini-replicons into A. tumefaciens C58C1 strains suggested that repABC1 functions as replicator genes but repABC2 does not in both the Ti plasmids. Because the components of repABC2 of pTiBo542 have highly similar amino acid and nucleotide sequences to those of the incRh1-type repABC replicon, we introduced repABC2-containing replicons into cells harboring an incRh1 plasmid in order to check their incompatibility traits. As a result, the repABC2-containing replicon expelled the resident incRh1 plasmid, indicating that the extra repABC locus is dispensable for replication and could work as an incompatibility determinant against incRh1 group plasmids. We suggest that the locus contributes to plasmid retention by eliminating the burden of co-existing competitive plasmids in host cells through its incompatibility.
致病农杆菌属中的Ti/Ri质粒是由repABC基因功能稳定维持的repABC复制子。据报道,分别属于IncRh2和IncRh4不相容群的两个Ti质粒pTiBo542和pTiS4携带两个repABC位点。在本研究中,为了揭示两个repABC位点在这两个质粒中的作用,我们构建了携带任一或两个repABC位点(此处称为repABC1和repABC2)的微型复制子,并检测了它们的复制和不相容特性。将微型复制子导入根癌农杆菌C58C1菌株表明,在这两个Ti质粒中,repABC1作为复制基因发挥作用,而repABC2则不然。由于pTiBo542的repABC2组件在氨基酸和核苷酸序列上与IncRh1型repABC复制子的组件高度相似,我们将含repABC2的复制子导入携带IncRh1质粒的细胞中,以检查它们的不相容特性。结果,含repABC2的复制子排出了驻留的IncRh1质粒,表明额外的repABC位点对于复制是可有可无的,并且可以作为针对IncRh1组质粒的不相容决定因素发挥作用。我们认为,该位点通过其不相容性消除宿主细胞中共存竞争质粒的负担,从而有助于质粒保留。