Cisgenesis and intragenesis as new strategies for crop improvement

Cisgenesis and intragenesis are emerging plant breeding technologies which offer great promise for future acceptance of genetically engineered crops. The techniques employ traditional genetic engineering methods but are confined to transferring of genes and genetic elements between sexually compatible species that can breed naturally. One of the main requirements is the absence of selectable marker genes (such as antibiotic resistance genes) in the genome. Hence the sensitive issues with regard to transfer of foreign genes and antibiotic resistance are overcome. It is a targeted technique involving specific locus; therefore, linkage drag that prolongs the time for crop improvement in traditional breeding does not occur. It has great potential for crop improvement using superior alleles that exist in the untapped germplasm or wild species. Cisgenic and intragenic plants may not face the same stringent regulatory assessment for field release as transgenic plants which is a clear added advantage that would save time. In this chapter, the concepts of cis/intragenesis and the prerequisites for the development of cis/intragenesis plants are elaborated. Strategies for marker gene removal after selection of transformants are discussed based on the few recent reports from various plant species

Efficient heat-shock removal of the selectable marker gene in genetically modified grapevine

Cisgenesis is one of the new plant breeding technologies emerging as a promising tool for the future, more publicly accepted than the traditional transgenic approach. One of the requirements for a cisgenic plant is the absence of selectable marker genes in the genome. In this study, a system for marker gene removal after selection of transgenic plants has been tested in grapevine. This is based on a binary vector containing a heat-shock-inducible promoter which, upon induction, activates a recombinase to produce the excision of a FRT-flanked box. After the removal of this cassette hosting both the marker gene, nptII, and the recombinase itself, the reporter gene gus may be expressed. Gene transfer experiments on grapevine embryogenic callus were carried out via Agrobacterium tumefaciens. Different heat-shock treatments with variable temperatures and heat incubations times were tested on a selected line and the optimal conditions for a complete removal of nptII with the subsequent gus transcription were found. Plants were analysed by means of qPCR on genomic DNA, to quantify nptII removal, and by a fluorimetric assay to measure gus activity. Our study is conceived as a proof-of-concept to investigate the feasibility of this method in grapevine in view of developing an efficient cisgenic approach in this valuable fruit cro