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No Evidence of Unexpected Transgenic Insertions in T1190 - A Transgenic Apple Used in Rapid Cycle Breeding - Following Whole Genome Sequencing

Zugehörigkeit
Research Division Plant Breeding, Agroscope, Switzerland
Patocchi, Andrea;
GND
1013858662
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Biosafety in Plant Biotechnology, Germany
Keilwagen, Jens;
GND
1172920559
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Biosafety in Plant Biotechnology, Germany
Berner, Thomas;
GND
1175585904
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Fruit Crops, Germany
Wenzel, Stephanie;
Zugehörigkeit
Swiss Federal Institute of Technology, Molecular Plant Breeding, Institute of Agricultural Sciences, ETH Zurich, Switzerland
Broggini, Giovanni A. L.;
Zugehörigkeit
Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK), Germany
Altschmied, Lothar;
GND
1059103400
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Fruit Crops, Germany
Hanke, Magda-Viola;
GND
128593652
Zugehörigkeit
Julius Kühn-Institute (JKI), Institute for Breeding Research on Fruit Crops, Germany
Flachowsky, Henryk

Rapid cycle breeding uses transgenic early flowering plants as crossbreed parents to facilitate the shortening of breeding programs for perennial crops with long-lasting juvenility. Rapid cycle breeding in apple was established using the transgenic genotype T1190 expressing the BpMADS4 gene of silver birch. In this study, the genomes of T1190 and its non-transgenic wild-type PinS (F1-offspring of 'Pinova' and 'Idared') were sequenced by Illumina short-read sequencing in two separate experiments resulting in a mean sequencing depth of 182× for T1190 and 167× for PinS. The sequencing revealed 8,450 reads, which contain sequences of ≥20 bp identical to the plant transformation vector. These reads were assembled into 125 contigs, which were examined to see whether they contained transgenic insertions or if they are not using a five-step procedure. The sequence of one contig represents the known T-DNA insertion on chromosome 4 of T1190. The sequences of the remaining contigs were either equally present in T1190 and PinS, their part with sequence identity to the vector was equally present in apple reference genomes, or they seem to result from endophytic contaminations rather than from additional transgenic insertions. Therefore, we conclude that the transgenic apple plant T1190 contains only one transgenic insertion, located on chromosome 4, and shows no further partial insertions of the transformation vector. Accession Numbers: JQ974028.1.

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Rechteinhaber: 2021 Patocchi, Keilwagen, Berner, Wenzel, Broggini, Altschmied, Hanke and Flachowsky.

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