Relationships among blueberry species within the section Cyanococcus of the Vaccinium genus based on EST-PCR markers

Commercial blueberry species of North America belong to the Vaccinium genus, section Cyanococcus. Phylogenetic relationships of 50 accessions of different ploidy levels within Cyanococcus were investigated using 249 expressed sequence tag-polymerase chain reaction markers and standard clustering methods. Of the commercial species, tetraploid V. corymbosum grouped most closely with the diploids, V. fuscatum and V. caesariense, followed by the diploid V. elliottii. Tetraploid V. angustifolium grouped with the diploids, V. boreale and V. myrtilloides. Hexaploid V. virgatum grouped most closely with the diploid V. tenellum, thus shedding light on the origins of these polyploid species.

Molecular Classification of Vicia faba L Genotypes by Using RAPD-PCR Markers

The research included the molecular classification study of seven genotypes of the bean Vicia faba L. (FBSPN2, TLD1266, TLD1814, TLB1266, Luzdeotono, favad and Histal. Using the RAPD technique for DNA, as 13 random primers were used, the products of inflation were transferred within the agarose gel, and the results of the study showed the possibility of separating the genotypes from each other and determining the degree of genetic variation between them, as the primers used produced (1002) packages of them (417 normal bundles and (585) mixed bundles. The genetic differences of the studied genotypes were determined to be distinguished by the number of bundles, as they reached (28) bundles, including (13) unique bundles and (15) absent bundles. The ILB1266 genotype showed the highest number of unique bundles, which It reached 4 bundles, while the cultivar Favad showed the absence of unique bundles in it, either bundles are absent. The genotypes (ILD1266, IILB1266, Luzdeotono) were distinguished for having the highest number, which amounted to (3) bundles. As for the FBSPN2 genotype, it did not have any absent bundle, and the primers varied. Of the resulting bundle sizes, their sizes ranged between bp (1925-130), and the highest value for the genetic dimension ranged between (0.110 - 0.269), as the lowest genetic dimension was between the two structures (FBSPN2 and ILD1266), which amounted to 0.110, and the highest value for the genetic dimension was (0.2 69) between the genotypes (ILD1266, HISTAL) (ILD1266, Luzdeotono) The Dendrogram shows the separation of the studied genotypes into two main groups, and each of them into two subgroups.

Identification and Characterization of DAMs Mutations Associated With Early Blooming in Sweet Cherry, and Validation of DNA-Based Markers for Selection

Dormancy release and bloom time of sweet cherry cultivars depend on the environment and the genotype. The knowledge of these traits is essential for cultivar adaptation to different growing areas, and to ensure fruit set in the current climate change scenario. In this work, the major sweet cherry bloom time QTL qP-BT1.1m (327 Kbs; Chromosome 1) was scanned for candidate genes in the Regina cv genome. Six MADS-box genes (PavDAMs), orthologs to peach and Japanese apricot DAMs, were identified as candidate genes for bloom time regulation. The complete curated genomic structure annotation of these genes is reported. To characterize PavDAMs intra-specific variation, genome sequences of cultivars with contrasting chilling requirements and bloom times (N = 13), were then mapped to the ‘Regina’ genome. A high protein sequence conservation (98.8–100%) was observed. A higher amino acid variability and several structural mutations were identified in the low-chilling and extra-early blooming cv Cristobalina. Specifically, a large deletion (694 bp) upstream of PavDAM1, and various INDELs and SNPs in contiguous PavDAM4 and -5 UTRs were identified. PavDAM1 upstream deletion in ‘Cristobalina’ revealed the absence of several cis-acting motifs, potentially involved in PavDAMs expression. Also, due to this deletion, a non-coding gene expressed in late-blooming ‘Regina’ seems truncated in ‘Cristobalina’. Additionally, PavDAM4 and -5 UTRs mutations revealed different splicing variants between ‘Regina’ and ‘Cristobalina’ PavDAM5. The results indicate that the regulation of PavDAMs expression and post-transcriptional regulation in ‘Cristobalina’ may be altered due to structural mutations in regulatory regions. Previous transcriptomic studies show differential expression of PavDAM genes during dormancy in this cultivar. The results indicate that ‘Cristobalina’ show significant amino acid differences, and structural mutations in PavDAMs, that correlate with low-chilling and early blooming, but the direct implication of these mutations remains to be determined. To complete the work, PCR markers designed for the detection of ‘Cristobalina’ structural mutations in PavDAMs, were validated in an F2 population and a set of cultivars. These PCR markers are useful for marker-assisted selection of early blooming seedlings, and probably low-chilling, from ‘Cristobalina’, which is a unique breeding source for these traits.

Population-genetic structure of the eastern sand lizard Lacerta agilis exigua (Reptiilia, Lacertidae), assessed by ISSR-PCR and IRAP-PCR markers

Впервые описано присутствие участков гомологии в геномах восточной прыткой ящерицы к длинным концевым повторам эндогенных ретровирусов Sabrina и SIRE-1 и выполнен сравнительный анализ спектров продуктов амплификации фрагментов геномной ДНК ящерицы Lacerta agilis exigua, полученных с использованием двух типов ДНК маркеров - фрагментов геномной ДНК, ящериц, фланкированных инвертированными повторами микросателлитных локусов и длинными концевыми повторами эндогенных ретровирусов The presence of homology regions in the long terminal repeats of the endogenous retroviruses Sabrina and SIRE - 1 in the genomes of the eastern sand lizard was described for the first time. A comparative analysis of the spectra of amplification products of genomic DNA fragments of the mentioned lizard species obtained using two types of DNA markers - fragments of genomic DNA, flanked by inverted repeats of microsatellite loci and long terminal repeats of endogenous retroviruses, was performed.

Molecular Genetic Analysis of Pinus sylvestris L. and Pinus sibirica Du Tour Populations in Perm Krai Based on Polymorphism ISSR-PCR markers

DNA polymorphism has been studied, indicators of genetic diversity and genetic structure of 3 populations of Pinus sylvestris L. and 3 populations of Pinus sibirica Du Tour in the Perm Krai have been determined. In the populations of P. sibirica, 102 ISSR-PCR markers were found, of which 88 were polymorphic (P95 = 0.863), and in the populations of P. sylvestris — 113 ISSR-PCR markers, 100 of which were polymorphic (P95 = 0.885). The populations of the two studied species of woody plants are characterized by high genetic diversity. At the same time, in P. sibirica, the indices of genetic diversity were slightly higher (HE = 0.195; ne = 1.335; na = 1.330) than in P. sylvestris (HE = 0.166; ne = 1.268; na = 1.212). The analysis of the genetic structure showed that the coefficient of genetic subdivision (GST) in the two studied species of the genus Pinus are similar and amount to 0.320 in P. sibirica and 0.303 in P. sylvestris. The populations of Siberian pine and Scots pine are characterized by an average degree of genetic differentiation, since the interpopulation component accounts for 32.0% and 30.3% of the genetic diversity of these species, respectively. Using the Mantel test, a high correlation was found between genetic and geographical distances in P. sibirica populations (R2 = 0.6871), while P. sylvestris showed a low correlation (R2 = 0.0649). The data obtained are relevant for the preservation of the gene pools of the studied two species of the genus Pinus in the Perm Krai.