This Article Full Text Full Text (PDF) All Versions of this Article: 145/4/1282    most recent pp.107.108092v1 Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via CrossRef Citing Articles via Web of Science (6) Citing Articles via Google Scholar Google Scholar Articles by Louwerse, J. D. Articles by Vergunst, A. C. Search for Related Content PubMed PubMed Citation Articles by Louwerse, J. D. Articles by Vergunst, A. C. Agricola Articles by Louwerse, J. D. Articles by Vergunst, A. C. Related Collections Vector Systems for Plant Research and Biotechnology

Stable Recombinase-Mediated Cassette Exchange in Arabidopsis Using Agrobacterium tumefaciens¹

Institute of Biology, Clusius Laboratory, Leiden University, 2333 AL Leiden, The Netherlands

Site-specific integration is an attractive method for the improvement of current transformation technologies aimed at the production of stable transgenic plants. Here, we present a Cre-based targeting strategy in Arabidopsis (Arabidopsis thaliana) using recombinase-mediated cassette exchange (RMCE) of transferred DNA (T-DNA) delivered by Agrobacterium tumefaciens. The rationale for effective RMCE is the precise exchange of a genomic and a replacement cassette both flanked by two heterospecific lox sites that are incompatible with each other to prevent unwanted cassette deletion. We designed a strategy in which the coding region of a loxP/lox5171-flanked bialaphos resistance (bar) gene is exchanged for a loxP/lox5171-flanked T-DNA replacement cassette containing the neomycin phosphotransferase (nptII) coding region via loxP/loxP and lox5171/lox5171 directed recombination. The bar gene is driven by the strong 35S promoter, which is located outside the target cassette. This placement ensures preferential selection of RMCE events and not random integration events by expression of nptII from this same promoter. Using root transformation, during which Cre was provided on a cotransformed T-DNA, 50 kanamycin-resistant calli were selected. Forty-four percent contained a correctly exchanged cassette based on PCR analysis, indicating the stringency of the selection system. This was confirmed for the offspring of five analyzed events by Southern-blot analysis. In four of the five analyzed RMCE events, there were no additional T-DNA insertions or they easily segregated, resulting in high-efficiency single-copy RMCE events. Our approach enables simple and efficient selection of targeting events using the advantages of Agrobacterium-mediated transformation.

² Present address: French National Institute for Health and Medical Research, ESPRI 26, UFR Médecine, CS83021, Avenue Kennedy, 30908 Nimes, France.

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: Paul J.J. Hooykaas (p.j.j.hooykaas{at}biology.leidenuniv.nl).

www.plantphysiol.org/cgi/doi/10.1104/pp.107.108092

^* Corresponding author; e-mail p.j.j.hooykaas{at}biology.leidenuniv.nl.

Received August 26, 2007; accepted September 27, 2007; published October 5, 2007.

This article has been cited by other articles:

				Z. Li, A. Xing, B. P. Moon, R. P. McCardell, K. Mills, and S. C. Falco Site-Specific Integration of Transgenes in Soybean via Recombinase-Mediated DNA Cassette Exchange Plant Physiology, November 1, 2009; 151(3): 1087 - 1095. [Abstract] [Full Text] [PDF]

				T. Tzfira, S. V. Kozlovsky, and V. Citovsky Advanced Expression Vector Systems: New Weapons for Plant Research and Biotechnology Plant Physiology, December 1, 2007; 145(4): 1087 - 1089. [Full Text] [PDF]