A transformation vector for the production of marker‐free transgenic plants containing a single copy transgene at high frequency

Summary We represent here the GST‐MAT vector system. The R recombinase gene of the site‐specific recombination system R /RS from Zygosaccharomyces rouxii was fused to the chemical inducible promoter of the glutathione‐S‐transferase (GST‐II‐27) gene from Zea mays . Upon excision, the isopentenyltransferase ( ipt ) gene that is used as a selectable marker gene is removed. When the cauliflower mosaic virus 35S promoter (CaMV 35S) was used to express R recombinase, 67% of the marker‐free transgenic plants had more than three transgene copies. Because the CaMV 35S promoter transiently and efficiently excised the ipt gene before callus and adventitious bud formation, the frequency of emergence of the ipt ‐shooty explants with a single T‐DNA copy might be reduced. In this study we show that the GST‐MAT vector efficiently produced transgenic ipt ‐shooty explants from 37 (88%) out of 42 differentiated adventitious buds and marker‐free transgenic plants containing the GUS gene from five (14%) out of 37 ipt ‐shooty lines. Furthermore, the GST‐MAT vector also induced two marker‐free transgenic plants without the production of ipt ‐shooty intermediates. Southern blot analysis showed that six (86%) out of seven marker‐free transgenic plants had a single GUS gene. This result suggests that the GST‐MAT vector is useful to generate high frequency, marker‐free transgenic plants containing a single transgene.