Microsatellite genotyping of carnation varieties.

A set of 11 sequence-tagged microsatellite markers for carnation (Dianthus caryophyllus) was developed using a DNA library enriched for microsatellites. Supplemented with three markers derived from sequence database entries, these were used to genotype carnation varieties using a semi-automated fluorescence-based approach. In a set of 82 cultivars, the markers amplified 4-16 alleles each. The effective number of alleles varied from 1.9 to 6.0. For the eight best scorable markers, heterozygosity was between 0.51 and 0.99. The markers were able to distinguish all cultivars with a unique combination of alleles, except for sport mutants, which were readily grouped together with the original cultivar. In addition, one group of three and one group of six cultivars each had the same combination of 'allelic peaks'. The cluster of three varieties concerned original cultivars and their mutants. The cluster of six consisted of four mutants from the same cultivar and two other varieties.

Construction and analysis of a microsatellite-based database of European wheat varieties.

A database of 502 recent European wheat varieties, mainly of winter type, was constructed using 19 wheat microsatellites and one secalin-specific marker. All datapoints were generated in at least two laboratories using different techniques for fragment analysis. An overall level of >99.5% accuracy was achieved. The 199 alleles detected allowed discrimination between all of the varieties except duplicates, and varieties derived from identical parents. Approximately 25% of the varieties showed some heterogeneities, with the highest level of heterogeneity in south-eastern European material. The highest genetic diversity and the highest number of rare alleles were found in varieties from southern Europe. The relative allele frequencies varied for most microsatellites in different geographical regions.

The role of peroxidases in pistil-pollen interactions.

The majority of pistil peroxidases are involved in processes related to growth, development and senescence. Only the tissue specific peroxidases in the transmitting tissue of the style may play a direct role in the regulation of pollen tube growth. The pollen peroxidases may function mainly in growth regulation and tube wall formation and play a role in the interaction between pollen and pistil by metabolizing the phenolic compounds in the pistil.

Mechanism of peroxidase isoenzyme induction in pollinated Nicotiana alata styles.

A comparative study on the induction of peroxidase isoenzymes, specifically number 10 (P-10) in Nicotiana alata styles revealed significant differences between the various plants of an inbred progeny. In some plants the ageing-induced increase in P-10 activity was very low, whereas in some others, it was relatively high. Pollination accelerated this increase, independent of the pollen genotype. Fertilization was followed by a considerable increase in the activity of several peroxidase isoenzymes, including P-10 in all the plants.Two plants that differed greatly with regard to P-10 induction were used in additional experiments in order to ascertain the mechanism involved in the induction of P-10. The increase in P-10 activity due to pollination or fertilization can partly be explained on the basis of auxin and auxin-induced ethylene activity. The differences in P-10 induction between various plants of the inbred progeny were probably due to differences in their sensitivity to ethylene.

S-specific proteins in styles of self-incompatible Nicotiana alata.

A comparison of the stigma protein patterns of individual plants of the inbred- and cross-progenies in Nicotiana alata by isoelectric focusing revealed the presence of S-specific proteins. The S allele-protein relationship was found for three different S alleles. The S-specific proteins occurred in both stigma and stylar parts of the pistil whereas they were absent in leaves. In clone OWL the concentration of S-specific proteins in the stigma increased gradually during floral development. The shift from compatibility to incompatibility was not accompanied by an abrupt increase in concentration of the S-proteins.

Do S allele-specific peroxidase isoenzymes exist in self-incompatible Nicotiana alata?

In order to test Pandey's hypothesis that peroxidase isoenzymes determine S-gene specificity in Nicotiana alata, peroxidase isoenzymes in styles and pollen from various plants of an inbred- and a cross progeny were compared by means of starch gel electrophoresis and electrofocusing.No relation between the S-genotype and the peroxidase isoenzyme patterns of pollen or of styles could be established. The differences between the isoenzyme patterns of different S-genotypes were ascribed to differences in the genetic background of various plants that had the same S-genotype.

Mentor pollen effects on gametophytic incompatibility in Nicotiana, Oenothera and Lycopersicum.

Attempts were made, through mentor pollen techniques, to overcome self-incompatibility in species belonging to the genera Nicotiana and Oenothera and in a hybrid of Lycopersicum, which are characterized by a gametophytic system of incompatibility. While radiation-killed incompatible pollen did not generate mentor effects in any of the material tested, radiation-killed compatible pollen was found to promote a high level of illegitimate fertilizations by incompatible pollen in N. alata. No evidence was obtained that radiation-killed compatible pollen could induce mentor effects in strictly self-incompatible clones of O. organensis and of the interspecific hybrid L. esculentum x L. peruvianum.