1101. [Transgenic tomato plants expressing recA and NLS-recA-licBM3 genes as a model for studying meiotic recombination].
- Author
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Komakhin RA, Komakhina VV, Miliukova NA, Goldenkova-Pavlova IV, Fadina OA, and Zhuchenko AA
- Subjects
- Bacterial Proteins genetics, Clostridium thermocellum enzymology, Genes, Reporter, Glycoside Hydrolases genetics, Solanum lycopersicum genetics, Solanum lycopersicum metabolism, Nuclear Localization Signals, Plants, Genetically Modified genetics, Plants, Genetically Modified metabolism, Plants, Genetically Modified physiology, Rec A Recombinases genetics, Recombinant Fusion Proteins genetics, Recombination, Genetic, Bacterial Proteins biosynthesis, Glycoside Hydrolases biosynthesis, Solanum lycopersicum physiology, Meiosis, Rec A Recombinases biosynthesis, Recombinant Fusion Proteins biosynthesis
- Abstract
Homologous DNA recombination in eukaryotes is necessary to maintain genome stability and integrity and for correct chromosome segregation and formation of new haplotypes in meiosis. At the same time, genetic determination and nonrandomness of meiotic recombination restrict the introgression of genes and generation of unique genotypes. As one of the approaches to study and induce meiotic recombination in plants, it is recommended to use the recA gene of Escherichia coli. It is shown that the recA and NLS-recA-licBM3 genes have maternal inheritance and are expressed in the progeny of transgenic tomato plants. Plants expressing recA or NLS-recA-licBM3 and containing one T-DNA insertion do not differ in pollen fertility from original nontransgenic forms and can therefore be used for comparative studies of the effect of bacterial recombinases on meiotic recombination between linked genes.
- Published
- 2010