Wang K, Herrera-Estrella A, Van Montagu M
Laboratorium voor Genetica, Rijksuniversiteit Gent, Belgium.
J Bacteriol. 1990 Aug;172(8):4432-40. doi: 10.1128/jb.172.8.4432-4440.1990.
The VirD1 and VirD2 proteins encoded by an inducible locus of the virulence (vir) region of the Agrobacterium tumefaciens Ti plasmid are required for site-specific nicking at T-DNA border sites. We have determined the nucleotide sequence of a 3.6-kilobase-pair fragment carrying the virD locus from nopaline Ti plasmid pTiC58. In contrast to the previous report (Hagiya et al., Proc. Natl. Acad. Sci. USA 82:2669-2673, 1985), we found that the first three open reading frames were capable of encoding polypeptides of 16.1, 49.7, and 21.4 kilodaltons. Deletion analysis demonstrated that the N-terminal conserved domain of VirD2 was absolutely essential for its endonuclease activity. When extra copies of the virD1 and virD2 genes were present in an A. tumefaciens strain carrying a Ti plasmid, increased amounts of T-strand and nicked molecules could be detected at early stages of vir induction. Such strains possessed the ability to transform plants with higher efficiency.
根癌土壤杆菌Ti质粒毒性(vir)区域的一个可诱导位点所编码的VirD1和VirD2蛋白,是T-DNA边界位点特异性切口形成所必需的。我们已经确定了携带来自胭脂碱型Ti质粒pTiC58的virD位点的一个3.6千碱基对片段的核苷酸序列。与之前的报道(Hagiya等人,《美国国家科学院院刊》82:2669 - 2673,1985)不同,我们发现前三个开放阅读框能够编码16.1、49.7和21.4千道尔顿的多肽。缺失分析表明,VirD2的N端保守结构域对其内切核酸酶活性绝对必要。当携带Ti质粒的根癌土壤杆菌菌株中存在额外拷贝的virD1和virD2基因时,在vir诱导的早期阶段可以检测到T链和切口分子的量增加。这样的菌株具有更高效率转化植物的能力。