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Gene Synthesis> | The DNA sequence of the Rpi-vnt1.1 gene of 4310 bp (GenBank accession FJ423044.1) was chemically synthesized and cloned into the vector pUC57 with additional XmaI restriction sites by GenScript Corp. (New Jersey USA). This DNA was cloned from S. venturii and contains the native promoter and transcript termination sequences flanking a coding sequence without intron. The XmaI fragment was sub-cloned into a dephosphorylated XmaI restricted pCAMBIA2300 plant transformation binary vector. The resulting gene construct, referred to as pCIP93, bears the Rpi-vnt1.1 gene and the nptII gene for kanamycin resistance between the right and left borders of its T-DNA (Fig. 1). pCIP93 was transferred by electroporation into the Agrobacterium tumefaciens hypervirulent strain EHA105 (Hood et al. 1993). | Get A Quote |
The Avr avirulence gene of Phytophthora infestans and R gene of the potato are the genetic components of the gene-for-gene interaction resulting in host plant resistance. This effector-triggered immunity has been recently exploited to generate extreme resistance to late blight in potato by genetic engineering. The choice of the R genes, their number forming a R gene stack, and the pathogen Avr gene diversity will likely determine how long this extreme resistance will last. Here, we report on a comparative study on the Rpi-vnt1.1 gene which originated from Solanum venturii, and was introduced in the potato variety ‘Desiree’ by genetic transformation, and the Avr-vnt1 gene from two isolates o... More