Tzfira Tzvi, Vaidya Manjusha, Citovsky Vitaly
Department of Biochemistry and Cell Biology, State University of New York, Stony Brook, New York 11794-5215, USA.
Nature. 2004 Sep 2;431(7004):87-92. doi: 10.1038/nature02857.
Genetic transformation of plant cells by Agrobacterium represents a unique case of trans-kingdom DNA transfer. During this process, Agrobacterium exports its transferred (T) DNA and several virulence (Vir) proteins into the host cell, within which T-DNA nuclear import is mediated by VirD2 (ref. 3) and VirE2 (ref. 4) and their host cell interactors AtKAP-alpha and VIP1 (ref. 6), whereas its integration is mediated mainly by host cell proteins. The factors involved in the uncoating of T-DNA from its cognate proteins, which occurs before integration into the host genome, are still unknown. Here, we report that VirF-one of the few known exported Vir proteins whose function in the host cell remains unknown-is involved in targeted proteolysis of VIP1 and VirE2. We show that VirF localizes to the plant cell nucleus and interacts with VIP1, a nuclear protein. VirF, which contains an F-box motif, significantly destabilizes both VIP1 and VirE2 in yeast cells. Destabilization of VIP1 in the presence of VirF was then confirmed in planta. These results suggest that VIP1 and its cognate VirE2 are specifically targeted by the VirF-containing Skp1-Cdc53-cullin-F-box complex for proteolysis. The critical role of proteasomal degradation in Agrobacterium-mediated genetic transformation was also evident from inhibition of T-DNA expression by a proteasomal inhibitor.
根癌农杆菌介导的植物细胞遗传转化代表了一种独特的跨王国DNA转移情况。在此过程中,根癌农杆菌将其转移(T)DNA和几种毒力(Vir)蛋白输出到宿主细胞中,在宿主细胞内,T-DNA的核输入由VirD2(参考文献3)和VirE2(参考文献4)及其宿主细胞相互作用蛋白AtKAP-α和VIP1(参考文献6)介导,而其整合主要由宿主细胞蛋白介导。在整合到宿主基因组之前,从其同源蛋白上解开T-DNA所涉及的因素仍然未知。在这里,我们报告VirF——少数已知的输出Vir蛋白之一,其在宿主细胞中的功能尚不清楚——参与VIP1和VirE2的靶向蛋白水解。我们表明VirF定位于植物细胞核并与核蛋白VIP1相互作用。含有F-box基序的VirF在酵母细胞中显著降低VIP1和VirE2的稳定性。然后在植物中证实了在VirF存在下VIP1的稳定性降低。这些结果表明,VIP1及其同源VirE2被含有VirF的Skp1-Cdc53-遍在蛋白连接酶-F-box复合物特异性靶向进行蛋白水解。蛋白酶体降解在根癌农杆菌介导的遗传转化中的关键作用也从蛋白酶体抑制剂对T-DNA表达的抑制中明显看出。