首页> 外文OA文献 >Genetic analysis of the virD operon of Agrobacterium tumefaciens: a search for functions involved in transport of T-DNA into the plant cell nucleus and in T-DNA integration.
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Genetic analysis of the virD operon of Agrobacterium tumefaciens: a search for functions involved in transport of T-DNA into the plant cell nucleus and in T-DNA integration.

机译:根癌农杆菌的virD操纵子的遗传分析:寻找参与将T-DNA转运到植物细胞核中以及参与T-DNA整合的功能。

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摘要

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.
机译:转移的DNA(T-DNA)从根癌农杆菌运输到细胞核,并稳定地整合到许多植物物种的基因组中。有人提出,紧密附着在T-DNA上的VirD2蛋白可将T-DNA引导到植物细胞核中,并参与整合。使用农杆菌感染和β-葡萄糖醛酸苷酶表达作为T-DNA转移的两种不同的非常敏感的瞬时分析方法,以及用于稳定整合的分析方法,我们已经表明,VirD2蛋白和VirD3蛋白的C端一半不参与T- DNA整合。然而,有效的T-DNA转移需要二倍核定位信号,该信号位于VirD2蛋白的C末端,并且先前已被证明能够将外源蛋白靶向到植物细胞核中。 。农杆菌感染显示virD4突变体在T-DNA转移中完全无活性。

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