Lin T S, Kado C I
Davis Crown Gall Group, University of California, Davis 95616.
Mol Microbiol. 1993 Aug;9(4):803-12. doi: 10.1111/j.1365-2958.1993.tb01739.x.
The virD operon of the resident Ti plasmid of Agrobacterium tumefaciens contains loci involved in T-DNA processing and undefined virulence functions. Nucleotide sequence of the entire virD operon of pTiC58 revealed similarities to the virD operon of the root-inducing plasmid pRiA4b and to that of the octopine-type plasmid pTiA6NC. However, comparative sequence data show that virD of pTiC58 is more akin to that of the pRiA4b than to that of the pTiA6NC. T7f10::virD gene fusions were used to generate polypeptides that confirm the presence of four open reading frames virD1, virD2, virD3, and virD4 within virD which have a coding capacity for proteins of 16.1, 49.5, 72.6, and 73.5 kDa, respectively. virD3 therefore encodes a polypeptide 3.4 times larger (72.6 versus 21.3 kDa) than that encoded by virD3 of octopine Ti plasmids. Non-polar virD4 mutants could not be complemented by a distant homologue, TraG protein of plasmid RP4. An independently regulated fifth ORF (orf5) is located immediately downstream of 3' end of virD4 and encodes a polypeptide of 97.4 kDa. The expression of orf5 is dependent on its own promoter and is independent of acetosyringone induction in A. tumefaciens. Recently, it has been shown that virD3 of octopine Ri or Ti plasmids is not required for virulence. In this report, we confirm and extend these findings on a nopaline Ti plasmid by using several virD non-polar mutants that were tested for virulence. virD3 and orf5 non-polar mutants showed no effect on tumorigenicity on 14 different plant species, while virD4 mutants lost their tumorigenicity completely on all these test plants. These data suggest that virD3 and orf5 are not essential for virulence whereas virD4 is absolutely required on a wide range of host plants.
根癌土壤杆菌的常驻Ti质粒的virD操纵子包含参与T-DNA加工的位点和未明确的毒力功能。pTiC58的整个virD操纵子的核苷酸序列显示出与根诱导质粒pRiA4b的virD操纵子以及章鱼碱型质粒pTiA6NC的virD操纵子相似。然而,比较序列数据表明,pTiC58的virD与pRiA4b的virD比与pTiA6NC的virD更相似。T7f10::virD基因融合用于产生多肽,证实了virD内存在四个开放阅读框virD1、virD2、virD3和virD4,它们分别对16.1、49.5、72.6和73.5 kDa的蛋白质具有编码能力。因此,virD3编码的多肽比章鱼碱Ti质粒的virD3编码的多肽大3.4倍(72.6 kDa对21.3 kDa)。非极性virD4突变体不能被远距离同源物质粒RP4的TraG蛋白互补。一个独立调控的第五个开放阅读框(orf5)位于virD4 3'端的紧邻下游,编码一个97.4 kDa的多肽。orf5的表达依赖于其自身的启动子,并且在根癌土壤杆菌中不依赖于乙酰丁香酮诱导。最近,已表明章鱼碱Ri或Ti质粒的virD3对毒力不是必需的。在本报告中,我们通过使用几个测试了毒力的virD非极性突变体,在胭脂碱Ti质粒上证实并扩展了这些发现。virD3和orf5非极性突变体对14种不同植物物种的致瘤性没有影响,而virD4突变体在所有这些测试植物上完全丧失了致瘤性。这些数据表明,virD3和orf5对毒力不是必需的,而virD4在广泛的宿主植物上是绝对必需的。