2012 Annual Report
Single copy transgenic Carrizo citrange founder lines will be generated containing the selection gene cassette flanked by fused recognition sites. An exchange venctor will be biolistcally transformed into the various Carrizo citrange founder lines. RMCE will be examined by negative slection and used to score the most effective pairs. The most effective Carrizo citrange founder lines and recombinase pairs will be published and made publicly available.
The targeting construct containing the recombinase platform has been completed and consists of the recombinase recognition sites for integration upstream of the positive/negative selection genes, Kan::codA. Kan is used for positive selection of transgenic citrus production while the codA gene will be used to detect successful recombination events. Downstream of the selection system are recognition sites for recombinase-mediated excision. Also included between the recombinase recognition sites is a minimal promoter beta-glucuronidase-Plus gene. This gene will allow detection of the targeting construct inserting into hyperactive chromosomal expression loci. This type of loci is desirable for high expression of transgenes. Due to the placement of the minimal promoter beta-glucuronidase-Plus between the recombinase recognition sites it will be removed during recombinase-mediated targeting. More recently a second version of the targeting construct has been completed with an improved selectable expression cassette. Efforts are now underway to complete the agro-bacterium based pEXCH vector, which will be used to deliver both recombinases (for Recombinase-Mediated Cassette Exchange) and genes of interest (for genomic insertion).
Carrizo has been transformed with the preliminary construct, to provide material for initial testing. To date more than 1,000 explants have been treated and 7 potential lines have been micrografted exvitro with more potentially transformed shoots continually being developed.