Transgenic tomato lines containing Ds elements at defined genomic positions as tools for targeted transposon tagging

• Published in: Molecular & general genetics Vol. 243; no. 6; p. 666
• Main Authors: Knapp, S, Larondelle, Y, Rossberg, M, Furtek, D, Theres, K
• Format: Journal Article
• Language: English
• Published: Germany 01-11-1994
• Subjects: Agrobacterium tumefaciens - genetics; Base Sequence; Chromosome Mapping; DNA Transposable Elements - genetics; Genome; Glucuronidase - genetics; Molecular Sequence Data; Mutagenesis, Insertional - genetics; Nucleotidyltransferases - genetics; Phosphotransferases (Alcohol Group Acceptor) - genetics; Plants, Genetically Modified - genetics; Transformation, Genetic; Transposases; Vegetables - genetics
• ISSN: 0026-8925
• DOI: 10.1007/bf00279576

We have introduced a genetically marked Dissociation transposable element (DsHPT) into tomato (Lycopersicon esculentum) by Agrobacterium tumefaciens-mediated transformation. Probes for the flanking regions of the T-DNA and transposed DsHPT elements were obtained with the inverse polymerase chain reaction (IPCR) technique and used in RFLP linkage analyses. The RFLP map location of 11 T-DNAs carrying DsHPT was determined. The T-DNAs are distributed on 7 of the 12 tomato chromosomes. To explore the feasibility of gene tagging strategies in tomato using DsHPT, we examined the genomic distribution of DsHPT receptor sites relative to the location of two different, but very closely linked, T-DNA insertion sites. After crosses with plants expressing Ac transposase, the hygromycin phosphotransferase (HPT) marker on the Ds element and the excision markers beta-glucuronidase (GUS) and Basta resistance (BAR) facilitated the identification of plants bearing germinally transposed DsHPT elements. RFLP mapping of 21 transposed DsHPT elements originating from the two different T-DNA insertions revealed distinct patterns of reintegration sites.