Protein Interactions Involved in Nuclear Import of the Agrobacterium VirE2 Protein in Vivo and in Vitro

• Published in: The Journal of biological chemistry 2004-07, Vol.279 (28), p.29528-29533
• Main Authors: Citovsky, Vitaly, Kapelnikov, Anat, Oliel, Shachar, Zakai, Nehama, Rojas, Maria R, Gilbertson, Robert L, Tzfira, Tzvi, Loyter, Abraham
• Format: Article
• Language: English
• Subjects: Active Transport, Cell Nucleus - physiology; Agrobacterium; alpha Karyopherins - metabolism; Animals; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Bacterial Proteins; Chlorocebus aethiops; COS Cells; DNA, Bacterial - metabolism; DNA-Binding Proteins - metabolism; Fluorescent Dyes - metabolism; HeLa Cells; Humans; Ion Channels - metabolism; Macromolecular Substances; Nicotiana - cytology; Nicotiana - metabolism; Nicotiana - microbiology; Nuclear Localization Signals; Plant Proteins - metabolism; Protein Binding; Rhizobium - genetics; Rhizobium - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M403159200

Agrobacterium , the only known organism capable of trans-kingdom DNA transfer, genetically transforms plants by transferring a segment of its DNA, T-DNA, into the nucleus of the host cell where it integrates into the plant genome. One of the central events in this genetic transformation process is nuclear import of the T-DNA molecule, which to a large degree is mediated by the bacterial virulence protein VirE2. VirE2 is distinguished by its nuclear targeting, which occurs only in plant but not in animal cells and is facilitated by the cellular VIP1 protein. The molecular mechanism of the VIP1 function is still unclear. Here, we used in vitro assays for nuclear import and quantification of protein-protein interactions to directly demonstrate formation of ternary complexes between VirE2, VIP1, and a component of the cellular nuclear import machinery, karyopherin α. Our results indicate that VIP1 functions as a molecular bridge between VirE2 and karyopherin α, allowing VirE2 to utilize the host cell nuclear import machinery even without being directly recognized by its components.