Koukolíková-Nicola Z, Raineri D, Stephens K, Ramos C, Tinland B, Nester E W, Hohn B
Friedrich Miescher-Institut, Basel, Switzerland.
J Bacteriol. 1993 Feb;175(3):723-31. doi: 10.1128/jb.175.3.723-731.1993.
The transferred DNA (T-DNA) is transported from Agrobacterium tumefaciens to the nucleus and is stably integrated into the genome of many plant species. It has been proposed that the VirD2 protein, tightly attached to the T-DNA, pilots the T-DNA into the plant cell nucleus and that it is involved in integration. Using agroinfection and beta-glucuronidase expression as two different very sensitive transient assays for T-DNA transfer, together with assays for stable integration, we have shown that the C-terminal half of the VirD2 protein and the VirD3 protein are not involved in T-DNA integration. However, the bipartite nuclear localization signal, which is located within the C terminus of the VirD2 protein and which has previously been shown to be able to target a foreign protein into the plant cell nucleus, was shown to be required for efficient T-DNA transfer. virD4 mutants were shown by agroinfection to be completely inactive in T-DNA transfer.
转移DNA(T-DNA)从根癌农杆菌转运至细胞核,并稳定整合到许多植物物种的基因组中。有人提出,紧密附着于T-DNA的VirD2蛋白引导T-DNA进入植物细胞核并参与整合过程。利用农杆菌介导的感染和β-葡萄糖醛酸酶表达作为两种不同的非常灵敏的T-DNA转移瞬时检测方法,以及稳定整合检测方法,我们已经证明VirD2蛋白的C端一半和VirD3蛋白不参与T-DNA整合。然而,位于VirD2蛋白C端内的双分型核定位信号,此前已证明其能够将外源蛋白靶向导入植物细胞核,结果表明该信号是高效T-DNA转移所必需的。通过农杆菌介导的感染表明,virD4突变体在T-DNA转移中完全无活性。