Starch gel electrophoresis of plant proteins was used to identify purple loosestrife (Lythrum spp.) cultivars and weedy populations. Preliminary determinations were made as to what degree weedy loosestrife populations were related (or genetically similar) to populations of L. alatum, L. virgatum, and horticultural cultivars. Cluster analysis of the data indicated that native L. alatum was genetically different from all populations of purple loosestrife and cultivars examined. The L. salicaria and L. virgatum cultivars, as groups, were not genetically distinguishable from the weedy populations analyzed. Seven cultivars of L. salicaria origin analyzed as a group were not distinguishable from the eight cultivars of L. virgatum origin, indicating that separation by cultivar origin may not be feasible. While the two “groups” were not distinguishable, most individual cultivars could be distinguished from one another by isozyme phenotype. Genetic variation was high within populations of weedy purple loosestrife but low among populations, which is characteristic of polyploid, perennial plant species that are widely distributed. Geographic location did not consistently correlate with genetic similarity.
The parents and progeny from two crosses (Cayuga White x Aurore and NY62.136.2 x Yates) were examined for the presence of DNA restriction fragment length polymorphisms (RFLPs). Seventeen independent DNA sequences were used in the analysis, 15 obtained from a grape Pst\ genomic library and two heterologous probes obtained from other laboratories. Most of the low copy cloned sequences hybridized to more than two restriction fragments, possibly reflecting the polyploid nature of the Vitis genome. Nine of the probes detected RFLPs between parents. Analysis of the progenies (F, generation) revealed segregation for nine distinct polymorphisms generated by seven of the probes. Thus, a relatively high level of polymorphism among parents, as well as heterozygosity within each parent, was evident. Most RFLPs gave segregation ratios close to the 1:1 ratio predicted for a locus heterozygous in one parent. However four differences between parental phenotypes did not segregate in the progeny, and in three instances fragments present in both parents segregated in the progeny. These peculiar results may be explained by accounting for heterozygosity or homozygosity, respectively, for the DNA segment that generates the polymorphism. We conclude that RFLP studies can be performed on the first filial generation in woody perennials such as Vitis that have a relatively high level of heterozygosity in the genome.
Isozyme markers were used to identify several cultivars of purple loosestrife (Lythrum spp.) and interspecific hybrids. There were three zones of activity for phosphoglucomutase (PGM) and phosphoglucoisomerase (PGI) and two zones for malate dehydrogenase (MDH) in purple loosestrife cultivars. Allelic constitution could not be characterized due to the polyploid nature of purple loosestrife and the possibility of intergenic dimerization. Coefficients of genetic similarity were used to estimate the degree of relationship between purple loosestrife cultivars. Cluster analysis indicated that seven cultivars originating from L. salicaria L. were not distinguishable from eight cultivars originating from L. virgatum L., indicating possible limitations of isozyme analysis for cultivar differentiation based on species origin. All but two cultivars (`Morden Gleam' and `Morden Rose') could be distinguished from one another by isozyme phenotype. This result suggests that isozymes may be useful for cultivar fingerprinting if additional isozyme systems could be resolved. `Robert' appeared morphologically heterogeneous, and plants could be differentiated based on isozyme banding patterns. Also, two putative clones of `Stichflamme' (one marketed under its English synonym `Fire Candle') possessed distinct isozyme phenotypes, indicating a lack of clonal integrity.
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