Russian Journal of Genetics (August 2010), 46 (8), pg. 960-966 by M. Smolik¹ ; I. Ochmian ²; J. Grajkowski ² ¹Department of Horticultural Plant Breeding, West Pomeranian University of Technology in Szczecin, Szczecin 71-422, Poland. email@example.com;²Department of Pomology
Inter-simple sequence repeat (ISSR) amplification was use d to analyze polymorphisms of micro-satellite sequences in the honeysuckle genome and to evaluate genetic diversity among fourteen Polish and Russian blue honeysuckle accessions (Lonicera caerulea var. edulis, L. caerulea no. 7661, L. caerulea no. 7987, Jolanta, Atut, Wojtek, Czarna, Zielona, Dlinnoplodna, Czelabinka, Signoglazka, N1, N2 and A). The plant material was selected from the Department of Pomology, the Dendrological Garden in Rogowo (Poland), and breeder collections. A total of 40 primers, containing different simple sequence repeat motifs, were tested for amplification. Out of the 40 primers, only 11 gave interpretable banding patterns in all blue honeysuckle accessions. A total of 129 ISSR loci were amplified, of which 83 (64%) were polymorphic and 24 (19%) accession-specific. ISSR-PCR with genomic DNA from blue honeysuckle yielded DNA fragments ranging from 260 to 3250 bp in size. UPGMA cluster analysis with bootstrapping (1000 replications) and used to construct a dendrogram and to estimate the genetic distances between Lonicera accessions. The ISSR-based phylogeny was consistent with Lonicera caerulea origin based on morphological and phenological evidence. The phylogenetic relationships based on the accession studies and the breeding usefulness are discussed.