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Seed proteins from the tetraploid Galeopsis tetrahit L. and its putative parental species G. pubescens Bess. and G. speciosa Mill., were examined using disc gel electrophoresis (PAGE), Ouchterlony double diffusion, and Immunoelectrophoresis. Forty‐three inbred cultivated lines of G. speciosa, G. pubescens, and G. tetrahit (both the naturally occurring species and an artificially produced hybrid) and two wild populations of G. tetrahit were examined. PAGE gels were stained for total protein or malate dehydrogenase. Although variability in the total protein pattern was detected within and between lines for all three species, there was much similarity among the taxa. No bands appeared in the hybrid that were not present in the parents. The band pattern for synthetic G. tetrahit was very similar to that of natural G. tetrahit suggesting that G. tetrahit originated from a cross in nature between G. pubescens and G. speciosa. The total protein PAGE results were analyzed using numerical taxonomic techniques. Although these analyses did not clearly separate the three species, the general tendency was toward grouping G. pubescens lines together, natural G. tetrahit lines together, and synthetic G. tetrahit lines together. Natural and synthetic G. tetrahit lines were also interspersed among each other along with some G. speciosa lines. The malate dehydrogenase pattern showed little variation among the three species. Qualitative serological methods did not distingush among the three species, but confirmed the similarity observed among the taxa in the results of electrophoresis.
Seed proteins from the tetraploid Galeopsis tetrahit L. and its putative parental species G. pubescens Bess. and G. speciosa Mill., were examined using disc gel electrophoresis (PAGE), Ouchterlony double diffusion, and Immunoelectrophoresis. Forty‐three inbred cultivated lines of G. speciosa, G. pubescens, and G. tetrahit (both the naturally occurring species and an artificially produced hybrid) and two wild populations of G. tetrahit were examined. PAGE gels were stained for total protein or malate dehydrogenase. Although variability in the total protein pattern was detected within and between lines for all three species, there was much similarity among the taxa. No bands appeared in the hybrid that were not present in the parents. The band pattern for synthetic G. tetrahit was very similar to that of natural G. tetrahit suggesting that G. tetrahit originated from a cross in nature between G. pubescens and G. speciosa. The total protein PAGE results were analyzed using numerical taxonomic techniques. Although these analyses did not clearly separate the three species, the general tendency was toward grouping G. pubescens lines together, natural G. tetrahit lines together, and synthetic G. tetrahit lines together. Natural and synthetic G. tetrahit lines were also interspersed among each other along with some G. speciosa lines. The malate dehydrogenase pattern showed little variation among the three species. Qualitative serological methods did not distingush among the three species, but confirmed the similarity observed among the taxa in the results of electrophoresis.
Serological analyses of soluble seed proteins of 12 representative taxa ofthe family Oleaceae by the techniques of Ouchterlony, presaturation, and immunoelectrophoresis (lEP) yielded complementary taxonomic information. Ouchterlony reactions differentiated among protein extracts of three species, and the combined serological techniques permitted the detection of protein differences of respective taxa of the two subfamilies Jasminoideae and Oleoideae. IEP enabled the separation of the 12 taxa investigated and the distribution into the two subfamilies, by the differential electrophoretic positions of precipitin arcs, which were consistent with members of each of the two subfamilies. Presaturation data, when analyzed by two cluster analysis computer programs, were taxonomically significant. One program, which calculated amalgamation distances from the presaturation data, clustered the 12 taxa into subgroups which corresponded to tribes, and within two groups, which corresponded to two subfamilies. A monothetic clustering program provided theoretical information on evolution of taxa within the family Oleaceae based on serological correspondences obtained from the presaturation data; the subfamily Jasminoideae was found phylogenetically primitive and the subfamily Oleoideae was advanced. Additionally, IEP data supported those theories suggesting that taxa of the Oleoideae evolved from taxa of the Jasminoideae. The groupings of taxa and different information obtained from the cluster analyses of data and all serological techniques reinforced each other, as well as contemporary taxonomic and phylogenetic treatments of taxa of the family Oleaceae.
Immunological affinities were investigated among twenty taxa belonging to the grass subfamilies Pooideae, Chloridoideae, Panicoideae, Oryzoideae, and Bambusoideae. Antisera were raised to the prolamin fraction of seed proteins from species of eleven grass genera (Hordeum, Bromus, Festuca, Phleum, Elensine, Panicum, Pennisetum, Tripsacum, Dendrocalamus, and Oryza) and reacted with their homologous antigens and nineteen different heterologous antigens in Enzyme‐Linked Immunosorbent Assay (ELISA). The immunological cross‐reactivity among the eleven taxa whose prolamin was used for antisera production was analyzed quantitatively by generating matrices of averaged cross‐reactivities, Q correlation and distance. The averaged cross‐reactivity matrix was calculated from averaging reciprocal immunological reactions while the two other matrices were computed by considering each antiserum as a character and antigens as OTUs. The three matrices were subjected to clustering by the Unweighted Pair Group Method using Arithmetic Averaging (UPGMA). The phenogram based on the averaged similarity matrix showed some distortion, while the other two phenograms were similar in topology and were informative. A phenon line at r = 0.17 divided the phenogram based on Q correlation into four major groups: Pooideae, Oryzoideae, Bambusoideae, and Chloridoideae‐Panicoideae. The two subfamilies in the Chloridoideae‐Panicoideae group clustered at a correlation coefficient of 0.22. Within the Pooideae, the tribes Aveneae and Agrostideae were closely grouped together (r = 0.85), but they were quite distinct (r = 0.16) from the tightly clustered (r = 0.84–0.85) Bromeae, Poeae, and Triticeae. The Oryzoideae and Bambusoideae showed low immunological similarity (r = –0.07). The two tribes of the Panicoideae, Paniceae and Andropogoneae, displayed extensive immunological similarity clustering tightly at r = 0.84–0.86. The immunological data revealed a possible trend in grass evolution encompassing the chloridoid‐panicoid groups and provided insights into the phylogenetic affinities of the bambusoid and oryzoid grasses. The results also underscored the heterogeneity of the taxa within the Pooideae.
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