Institute of Plant Physiology and Institute of Genetics, Biological Research Center, Hungarian Academy of Sciences, H-6701, Szeged POB 521, Hungary.
Theor Appl Genet. 1992 Sep;84(7-8):880-90. doi: 10.1007/BF00227400.
Asymmetric somatic hybrids between Solanum tuberosum L. and S. brevidens Phil. have been obtained via the fusion of protoplasts from potato leaves and from cell suspension culture of S. brevidens. The wild Solanum species served as donor after irradiation of its protoplasts with a lethal X-ray dose (200 Gy). Selection of the putative hybrids was based on the kanamycin-resistance marker gene previously introduced into the genome of Solanum brevidens by Agrobacterium-mediated gene transfer. Thirteen out of the 45 selected clones exhibited reduced morphogenic potential. The morphological abnormalities of the regenerated plantlets were gradually eliminated during the extended in vitro culture period. Cytological investigations revealed that the number of chromosomes in the cultured S. brevidens cells used as protoplast source ranged between 28-40 instead of the basic 2n=24 value. There was a high degree of aneuploidy in all of the investigated hybrid clones, and at least 12 extra chromosomes were observed in addition to the potato chromosomes (2n=48). Interand intraclonal variation and segregation during vegetative propagation indicated the genetic instability of the hybrids, which can be ascribed to the pre-existing and X-ray irradiation-induced chromosomal abnormalities in the donor S. brevidens cells. The detection of centromeric chromosome fragments and long, poly-constrictional chromosomes in cytological preparations as well as non-parental bands in Southern hybridizations with restriction fragment length polymorphism (RFLP) markers revealed extensive chromosome rearrangements in most of the regenerated clones. On the basis of the limited number of RFLP probes used, preferential loss of S. brevidens specific markers with a non-random elimination pattern could be detected in hybrid regenerants.
已通过融合来自马铃薯叶片的原生质体和来自短日照茄悬浮细胞培养物的原生质体,获得了马铃薯和短日照茄的不对称体细胞杂种。在对其原生质体进行致死剂量(200Gy)X 射线照射后,野生茄属植物作为供体。对可能的杂种的选择是基于先前通过农杆菌介导的基因转移引入短日照茄基因组的卡那霉素抗性标记基因。在 45 个选定的克隆中有 13 个表现出形态发生潜力降低。在延长的体外培养期间,再生植株的形态异常逐渐消除。细胞学研究表明,用作原生质体来源的培养短日照茄细胞的染色体数介于 28-40 之间,而不是基本的 2n=24 值。在所研究的杂种克隆中均存在高度的非整倍性,除了马铃薯染色体(2n=48)之外,还观察到至少 12 条额外的染色体。在营养繁殖期间的种内和种间变异和分离表明杂种的遗传不稳定性,这可归因于供体短日照茄细胞中存在的和 X 射线照射诱导的染色体异常。在细胞学制剂中检测到着丝粒染色体片段和长的、多缢缩的染色体,以及与限制性片段长度多态性(RFLP)标记的Southern 杂交中的非亲本带,揭示了大多数再生克隆中的广泛染色体重排。基于所使用的有限数量的 RFLP 探针,可以检测到杂种再生体中 S. brevidens 特异性标记物的优先丢失,其具有非随机消除模式。