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ISSR-PCR markers were used to assess genetic diversity and to elucidate relatedness among 21 Ukrainian and 3 West European sweet cherry varieties, which are widely cultivated in Ukraine. The discriminatory potential was tested for 11 ISSR-PCR primers, which produced 193 amplicons. UBC 835, 836, 841 and 881 were identified as the best primers suitable for routine application. The studied cultivars appear to be genetically highly heterogenic and can be divided in two main groups. The first one includes closely related cultivars obtained by hybridization of Drogan’s Yellow (Drogans gelbe Knorpelkirsche), Valerii Chkalov and some other forms. The second group comprises less similar cultivars derived from several West-European and unknown ancestors. Origin of several Ukrainian cultivars is discussed.

The article shortly describes the life path of Erwin Chargaff, one of the most famous figures in the history of molecular biology and genetics. Chargaff was born in Chernivtsi (Austria-Hungary, now Ukraine) but during the First World War his family was forced to move to Vienna. After graduating from the University of Vienna, Chargaff worked in Berlin, where he studied bacterial lipids. Due to Nazis coming to power in Germany, Chargaff moved to Paris and later (1935) emigrated to the USA and obtained a position at Columbia University, where he initially investigated the role of phospholipids in blood clotting. In 1944, applying novel methods Chargaff initiated intensive investigation of the chemical composition of nucleic acids from taxonomically distant species and established two rules which were later named after him. The first Chargaff's rule provided a significant support to Watson and Crick in construction of their double helical DNA model. The explosion of atomic bombs over Hiroshima and Nagasaki forced Chargaff to think about the moral responsibility of researchers and science to mankind. He begins to raise these issues in the press and manifests himself as a talented journalist, who criticized the bureaucratization of science and its transformation into a way of earning money. Despite decades of life in America, spiritually Erwin Chargaff always remained a European, who never forgot his roots and always remembered his native land.

In order to clarify molecular organization of the genomic region encoding 5S rRNA in diploid species Rosa rugosa several 5S rDNA repeated units were cloned and sequenced. Analysis of the obtained sequences revealed that only one length variant of 5S rDNA repeated units, which contains intact promoter elements in the intergenic spacer region (IGS) and appears to be transcriptionally active is present in the genome. Additionally, a limited number of 5S rDNA pseudogenes lacking a portion of coding sequence and the complete IGS was detected. A high level of sequence similarity (from 93.7 to 97.5%) between the IGS of major 5S rDNA variants of East Asian R. rugosa and North American R. nitida was found indicating comparatively recent divergence of these species.

Two length variants of 5S rDNA repeated units were detected in the genome of East European butterfly Melitaea trivia. Both repeat variants contain the 5S rRNA coding region of the same length of 120 bp, but possess the intergenic spacer region (IGS) of different size, 78 and 125 bp, respectively. The level of sequence similarity between the two 5S rDNA variants amounts to 43.9-45.5% in the IGS, whereas the coding region appears to be more conservative. In the IGS, microsatellite sequence motives were found; amplification of these motives could be involved in the evolution of the 5S rDNA.

An approximately 135-bp sequence called the A1/A2 repeat was isolated from the transcribed region of the 26-18S rDNA intergenic spacer (IGS) of Nicotiana tomentosiformis. Fluorescence in situ hybridization (FISH) and Southern blot analysis revealed its occurrence as an independent satellite (termed an A1/A2 satellite) outside of rDNA loci in species of Nicotiana section Tomentosae. The chromosomal location, patterns of genomic dispersion, and copy numbers of its tandemly arranged units varied between the species. In more distantly related Nicotiana species the A1/A2 repeats were found only at the nucleolar organizer regions (NOR). There was a trend toward the elimination of the A1/A2 satellite in N. tabacum (tobacco), an allotetraploid with parents closely related to the diploids N. sylvestris and N. tomentosiformis. This process may have already commenced in an S(3) generation of synthetic tobacco. Cytosine residues in the IGS were significantly hypomethylated compared with the A1/A2 satellite. There was no clear separation between the IGS and satellite fractions in sequence analysis of individual clones and we found no evidence for CG suppression. Taken together the data indicate a dynamic nature of the A1/A2 repeats in Nicotiana genomes, with evidence for recurrent integration, copy number expansions, and contractions.

Ribosomal DNA comprises a considerable part of a plant genome and is organized in tandemly arranged repeats composed of conservative coding sequences for ribosomal RNA and rapidly evolving spacer elements. We determined the nucleotide sequences of intergenic spacer regions (IGS) for five species from Solanacaea family: Solanum tuberosum, Atropa belladonna, Nicotiana tabacum, N. tomentosiformis, and N. sylvestris. The detailed comparative analysis of these and some other rDNA sequences allowed us to reveal the general regularities of evolution and functional organization of the rDNA spacer region and to clarify better phylogenetic relationships between the species within Solanacea family. A large body of experimental data on the application of rDNA in plant breeding, taxonomical studies and biotechnology are provided and discussed.

Origin and rearrangement of ribosomal DNA repeats in natural allotetraploid Nicotiana tabacum are described. Comparative sequence analysis of the intergenic spacer (IGS) regions of Nicotiana tomentosiformis (the paternal diploid progenitor) and Nicotiana sylvestris (the maternal diploid progenitor) showed species-specific molecular features. These markers allowed us to trace the molecular evolution of parental rDNA in the allopolyploid genome of N. tabacum; at least the majority of tobacco rDNA repeats originated from N. tomentosiformis, which endured reconstruction of subrepeated regions in the IGS. We infer that after hybridization of the parental diploid species, rDNA with a longer IGS, donated by N. tomentosiformis, dominated over the rDNA with a shorter IGS from N. sylvestris; the latter was then eliminated from the allopolyploid genome. Thus, repeated sequences in allopolyploid genomes are targets for molecular rearrangement, demonstrating the dynamic nature of allopolyploid genomes.

It has been found that Cu and Ni at contents of 17 mg/kg and 64 mg/kg dry weight respectively in leaves tissues have no visible effect on morphological and physiological characteristics of plants and increase [3H]uridine incorporation in various types of RNA. Under these conditions synthesise of nuclear RNA has been found 1.8-2.4 more intense, transport RNA -2.0-2.8 intense and ribosomal RNA-1.2-2.8 intense in comparison with control. Analysing our data it is possible to suggest that the activation of the RNA synthesis under the heavy metals influence may be one of the protective mechanism connected with the plant cell adaptation to the stressful conditions.

The nucleotide sequence of the intergenic spacer (IGS) region between the 25S and the 18S rRNA coding regions has been determined for tobacco (Nicotiana tabacum). The IGS (5140 bp in length) can be subdivided into several regions (I-VII) two of which, upstream and downstream of the putative transcription initiation site (TIS), contain prominent subrepeats (A and C). The unique sequence in the central part of the IGS (region IV) preceding the TIS is extremely AT-rich. The distance from the putative TIS to the 5' end of the 18S rRNA gene is 3005 bp. The IGS sequences are compared with potato (Solanum tuberosum) and tomato (Lycopersicon esculentum) IGS. Restriction mapping of 13 Nicotiana species shows that considerable rDNA repeat length heterogeneity in this genus is probably due to different numbers of A and C subrepeats.

14C-leucine incorporation in cytoplasmic protein was compared for three haploid forms, three derivative autodiploid lines and four hybrid forms of maize. It has been found that the precursor incorporation in the haploid forms was by 15-20% higher that in appropriate autodiploid lines. However, the level of protein synthesis wes practically the same for all investigated diploid forms. Thus, the increase of the ploidy level correlates with the decrease of the cytoplasmic protein synthesis. It was also shown that the protein content was practically equal in haploid and diploid forms. Proceeding from the authors' data one can conclude that the protein distraction may also have different intensity. The next step of the investigation was the study of the effects of the chemical factor of cytoplasmic protein synthesis in maize seedlings with different ploidy levels in vivo. It has been revealed, that the rate of 14C-leucine incorporation in the cytoplasmic proteins differ for the haploid forms which grew on the Knop media with the addition of phenol (0.05%) and without pollutant. Nevertheless, approximately equal level of 14C-leucine incorporation was observed for autodiploids. Recently it was demonstrated that the synthetic intensity of different RNA fractions is higher in the haploid maize forms than in the diploid ones and that the haploid and diploid forms of maize display the different reaction on phenol pollution. When comparing our data with the published results it is possible to conclude that the hypothesis about the low intensity of metabolism in haploid plants, existing in literature, is not true. The authors suppose that the high activity of synthesis of nuclear, transfer and ribosomal RNA and cytoplasmic proteins in the haploid plants may be connected with high mitotic activity. The authors' data are in agreement with the hypothesis that the ratio of nuclear volume and surface determines the metabolism rate.