Moriguchi K, Maeda Y, Satou M, Hardayani N S, Kataoka M, Tanaka N, Yoshida K
Department of Biological Science, Graduate School of Science, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
J Mol Biol. 2001 Mar 30;307(3):771-84. doi: 10.1006/jmbi.2001.4488.
The Ri (root-inducing) plasmid in Agrobacterium rhizogenes and Ti (tumor-inducing) plasmid in Agrobacterium tumefaciens have provided the fundamental basis for the construction of plant vectors and transgenic plants. Recently, the determination of the first complete nucleotide sequence of the Ti plasmid (pTi-SAKURA) has been successful. To understand the general structure of these oncogenic T-DNA transfer plasmids, the whole nucleotide sequence of a mikimopine-type Ri plasmid, pRi1724, was analyzed. The plasmid is 217,594 bp in size, and has 173 open reading frames (ORFs) in total, which are asymmetrically distributed. Except for 27 ORFs, which are unknown, 173 ORFs were classified into 12 groups as follows: three for DNA replication, nine for plasmid modification, 22 for conjugation, 26 for virulence, 11 for T-DNA gene, 19 for mikimopine/mikimopine-lactam transport, ten for an unknown opine metabolism, seven for transcriptional regulator, five for sugar transport, five for glycerol metabolism, four for chemoreceptor and 32 for others. The elucidated chimeric structure of pRi1724 interestingly indicates that the evolution of Rhizobiaceae plasmids seems to have kept interactions among the plasmids; especially, the genes and elements for a conjugal transfer of pRi1724 had clearly closer kinship to those of a Sym (symbiotic) plasmid, pNGR234a in Rhizobium sp. than those of Ti plasmids. By using sequencing and Northern analysis, we examined the metabolic pathway and gene expression of mikimopine, which is probably an Ri-specific opine.
发根农杆菌中的Ri(发根诱导)质粒和根癌农杆菌中的Ti(肿瘤诱导)质粒为植物载体和转基因植物的构建提供了基础。最近,成功测定了Ti质粒(pTi-SAKURA)的首个完整核苷酸序列。为了解这些致癌T-DNA转移质粒的总体结构,分析了一种甘露碱型Ri质粒pRi1724的全核苷酸序列。该质粒大小为217,594 bp,共有173个开放阅读框(ORF),分布不对称。除27个未知的ORF外,173个ORF被分为12组,如下:3个用于DNA复制,9个用于质粒修饰,22个用于接合,26个用于毒性,11个用于T-DNA基因,19个用于甘露碱/甘露碱-内酰胺转运,10个用于未知的冠瘿碱代谢,7个用于转录调节因子,5个用于糖转运,5个用于甘油代谢,4个用于化学感受器,32个用于其他。pRi1724阐明的嵌合结构有趣地表明,根瘤菌科质粒的进化似乎保持了质粒之间的相互作用;特别是,pRi1724接合转移的基因和元件与根瘤菌属中Sym(共生)质粒pNGR234a的基因和元件的亲缘关系明显比与Ti质粒的更近。通过测序和Northern分析,我们研究了甘露碱(可能是一种Ri特异性冠瘿碱)的代谢途径和基因表达。