Abstract
The reasons for subjecting the tomato eultivar, Lycopersicon esculentum, to numerous cell and tissue culture studies have been twofold: agronomic improvement of this important crop species and exploitation of tomatO’s abundant classical genetics for basic research purposes. Several years ago we began experiments utilizing protoplasts of Lycopersicon species, with the goals of developing methods to culture and regenerate plants, influencing transmission of genomes following cell fusion, and genetically analyzing plants resulting from protoplast or fusion product regeneration. At the time, little information was available about the requirements for successful culture and regeneration of members of the tomato genus. We looked to the facile protoplast culture and fusion of other Solanaceous species, Nicotiana and Petunia, as guides, as well as the arduous but effective methods for potato protoplasts developed by Shepard et al. (1980). Here we will summarize our knowledge of Lycopersicon protoplast culture and fusion and the analysis of regenerated plants.
A portion of this article has been derived (with permission) from one previously published in the Iowa State Journal for Research (Hanson et al. 1987). The literature review for this article was completed in 1986
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Hanson, M.R., O’Connell, M.A., Vidair, C. (1989). Somatic Hybridization in Tomato. In: Bajaj, Y.P.S. (eds) Plant Protoplasts and Genetic Engineering I. Biotechnology in Agriculture and Forestry, vol 8. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73614-8_22
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DOI: https://doi.org/10.1007/978-3-642-73614-8_22
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