Is VIP1 important for Agrobacterium‐mediated transformation?

• Published in: The Plant journal : for cell and molecular biology 2014-09, Vol.79 (5), p.848-860
• Main Authors: Shi, Yong, Lee, Lan‐Ying, Gelvin, Stanton B
• Format: Article
• Language: English
• Subjects: Agrobacterium; Agrobacterium - genetics; Agrobacterium - physiology; Arabidopsis; Arabidopsis - genetics; Arabidopsis - metabolism; Arabidopsis - microbiology; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Arabidopsis thaliana; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Basic-Leucine Zipper Transcription Factors - genetics; Basic-Leucine Zipper Transcription Factors - metabolism; Botany; Cell Nucleus - metabolism; cytoplasm; Cytoplasm - metabolism; DNA; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; gene overexpression; genetically modified organisms; genome; Genomics; Ion Channels - genetics; Ion Channels - metabolism; leaves; mesophyll; microscopy; mutants; Nicotiana - genetics; Nicotiana - metabolism; Nicotiana benthamiana; Plant Leaves - genetics; Plant Leaves - metabolism; Plant Leaves - microbiology; plant transformation; Plants, Genetically Modified; protein subcellular localization; Protein Transport; Proteins; protoplasts; roots; tobacco; Transformation, Genetic; Venus; VirE2; VirE2 interacting protein 1
• ISSN: 0960-7412; 1365-313X
• DOI: 10.1111/tpj.12596

Agrobacterium genetically transforms plants by transferring and integrating T‐(transferred) DNA into the host genome. This process requires both Agrobacterium and host proteins. VirE2 interacting protein 1 (VIP1), an Arabidopsis bZIP protein, has been suggested to mediate transformation through interaction with and targeting of VirE2 to nuclei. We examined the susceptibility of Arabidopsis vip1 mutant and VIP1 overexpressing plants to transformation by numerous Agrobacterium strains. In no instance could we detect altered transformation susceptibility. We also used confocal microscopy to examine the subcellular localization of Venus‐tagged VirE2 or Venus‐tagged VIP1, in the presence or absence of the other untagged protein, in different plant cell systems. We found that VIP1–Venus localized in both the cytoplasm and the nucleus of Arabidopsis roots, agroinfiltrated Nicotiana benthamiana leaves, Arabidopsis mesophyll protoplasts and tobacco BY‐2 protoplasts, regardless of whether VirE2 was co‐expressed. VirE2 localized exclusively to the cytoplasm of tobacco and Arabidopsis protoplasts, whether in the absence or presence of VIP1 overexpression. In transgenic Arabidopsis plants and agroinfiltrated N. benthamina leaves we could occasionally detect small aggregates of the Venus signal in nuclei, but these were likely to be imagining artifacts. The vast majority of VirE2 remained in the cytoplasm. We conclude that VIP1 is not important for Agrobacterium‐mediated transformation or VirE2 subcellular localization.