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Theor Appl Genet. 1993 Apr;86(2-3):377-82. doi: 10.1007/BF00222105.
Asymmetric somatic hybrid plants were recovered after fusing irradiated mesophyll protoplasts of donor Lycopersicon esculentum × L. pennellii (EP) interspecific hybrid with callus-derived protoplasts of recipient Solanum lycopersicoides. EP plant A54 had been previously transformed by an agrobacterium vector, and the T-DNA insert mapped to the L. esculentum chromosome 12. The T-DNA insert conferred kanamycin resistance to EP that was subsequently used to select cell fusion products and recover asymmetric hybrid plants that retained tagged chromosome 12. Doses of 50- and 100-Gy irradiation promoted the elimination of only a few donor chromosomes. At 200 Gy, the regenerated plants had ploidy levels higher than tetraploid. However, the T-DNA tagged chromosome 12 was always retained in the asymmetric hybrid plants tested. Likewise, all plants from the 100-Gy series, with the exception of number 160, were mixoploid in the root-tip cells. Such mixoploid asymmetric somatic hybrids could be stabilized by inducing adventitious shoots on leaf strips cultured on shoot regeneration medium containing kanamycin. The asymmetric hybrid plants did not produce viable seed when self-pollinated or backcrossed to tomato or S. lycopersicoides.
融合了供体番茄×李番茄(EP)种间杂种的照射叶肉原生质体和受体普通番茄野生种(Solanum lycopersicoides)愈伤组织衍生的原生质体后,获得了不对称体细胞杂种植株。先前已通过农杆菌载体转化了 EP 植株 A54,并且 T-DNA 插入物定位到了番茄 12 号染色体上。T-DNA 插入赋予 EP 卡那霉素抗性,随后用于选择细胞融合产物并回收保留标记染色体 12 的不对称杂种植物。50Gy 和 100Gy 的照射剂量仅促进了少数供体染色体的消除。在 200Gy 时,再生植株的倍性水平高于四倍体。然而,在所测试的不对称杂种植物中,始终保留了带有 T-DNA 标记的 12 号染色体。同样,除了 160 号之外,100Gy 系列中的所有植物在根尖细胞中都是混倍体。通过在含有卡那霉素的芽再生培养基上培养叶片条来诱导不定芽,可以稳定这种混倍体不对称体细胞杂种。当自交或回交到番茄或普通番茄野生种时,不对称杂种植物不能产生有活力的种子。