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Plant Physiology 140:1205-1212 (2006)
© 2006 American Society of Plant Biologists

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BREAKTHROUGH TECHNOLOGIES

Use of Bacterial Quorum-Sensing Components to Regulate Gene Expression in Plants1,[W]

Young-Sook You, Heather Marella, Rodolfo Zentella2, Yiyong Zhou, Tim Ulmasov, Tuan-Hua David Ho and Ralph S. Quatrano*

Department of Biology, Washington University, St. Louis, Missouri 63130 (Y.-S.Y., H.M., R.Z., Y.Z., T.-H.D.H., R.S.Q.); and Monsanto Company, St. Louis, Missouri 63167 (T.U.)

We describe an efficient inducible system to regulate gene expression in plants based on quorum-sensing components found in Gram-negative bacteria such as Agrobacterium tumefaciens. These bacteria monitor their own population density by utilizing members of the N-acyl homoserine lactone family as inducers and a transcriptional activator as its receptor. In our study, we utilize the components from A. tumefaciens (i.e. 3-oxooctanyl-L-homoserine lactone [OOHL]) synthesized by the TraI protein and its receptor, TraR. When OOHL binds to TraR, it recognizes its specific cis-element, the tra box. We translationally fused the eukaryotic VP16 activation domain to the N terminus of TraR. In the presence of OOHL, the chimeric VP16:TraR transcriptional regulator induces reporter gene expression in moss (Physcomitrella patens), barley (Hordeum vulgare), and carrot (Daucus carota) cells, as well as in transgenic Arabidopsis (Arabidopsis thaliana) seedlings. The inducible system shows a low level of reporter gene expression in the absence of the inducer. Foliar application and a floating-leaf assay in the presence of the inducer shows a 30- and 200-fold induction, respectively. Induction by foliar application of the inducer to whole seedlings is achieved within 8 h. The VP16:TraR activator also shows specificity for binding to its cognate inducer, OOHL. Based on microarray analyses, endogenous gene expression is not significantly affected due to overexpression of the TraR protein or presence of OOHL in either wild-type or lactone-inducible transgenic plants.


1 This work was supported by the Monsanto/Washington University Plant Science Agreement.

2 Present address: Department of Biology, Duke University, Durham, NC 27708.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Ralph S. Quatrano (rsq{at}wustl.edu).

[W] The online version of this article contains Web-only data.

www.plantphysiol.org/cgi/doi/10.1104/pp.105.074666.

* Corresponding author; e-mail rsq{at}wustl.edu; fax 314–935–8692.

Received November 23, 2005; returned for revision January 31, 2006; accepted February 1, 2006.


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