Mean Heterozygosity Values Research Articles

SSR-marker assisted evaluation of genetic diversity in local and exotic pigeonpea cultivars in Benin for parental genotypes selection

Pigeonpea production is limited in Benin due to the undesirable agronomic and organoleptic characteristics of cultivated landraces. For a breeding program, some exotic cultivars were introduced for improving the available genepool in the country. The present study aims to assess the genetic diversity within a collection comprising of 32 local and 28 exotic cultivars, with the objective of selecting suitable parental lines for pigeonpea genetic improvement. All of the 60 accessions were genotyped with 14 SSR makers and a total of 38 alleles were detected with an average of 2.71 alleles per locus. The mean value of PIC (Polymorphism Information Content) and overall gene diversity were 0.37 and 0.43, respectively, while the mean value of heterozygosity was 0.11, indicating moderate genetic diversity within the 60 accessions with a deficit of heterozygous genotypes. As expected, the diversity was higher in exotic cultivars than in local landraces. Based on the genetic relationship among accessions, the entire collection formed 3 clusters, one of which comprised four specific exotic accessions. Population structure analysis using model-based and DAPC (Discriminant Analysis for Principal Components) methods subdivided the 60 accessions into two major groups reflecting their geographic origins with a minimal number (02) of admixtures. This indicates significant genetic divergence between local and exotic cultivars. Analysis of Molecular Variance (AMOVA) results with an overall Fst value of 0.13 confirmed the significant genetic divergence between the two collections. The findings of this study will significantly benefit for pigeonpea breeding programs in Benin. For practical applications, selected exotic cultivars, particularly those within the specific cluster can immediately serve as donor parents in crossbreeding schemes with the local landraces, for developing new varieties.

Characterization of Okra (Abelmoschus esculentus L.) Accessions with Variable Drought Tolerance through Simple Sequence Repeat Markers and Phenotypic Traits

Genetic diversity analysis of crop genetic resources is a prerequisite for parental selection with suitable and complementary profiles for breeding. The objectives of this study were to determine genetic diversity present among okra accessions using simple sequence repeat (SSR) and complementary phenotypic markers and to select genetically divergent and superior parental accessions for pre-breeding. Twenty-six preliminarily selected okra accessions were assessed using nine highly polymorphic SSR markers and phenotyped under drought-stressed (DS) and non-stressed (NS) environmental conditions using a 13 × 2 alpha lattice design with two replications. Data were collected on the following eleven phenotypic traits: plant height (PH), days to 50% maturity (DTM), fresh pod length (FPL), dry pod weight (DPW), dry pod length (DPL), number of pods per plant (NPPP), pod yield per plant (PYPP), total above-ground biomass (AGB), harvest index (HI), root weight (RW), and root to shoot ratio (RSR). The SSR markers revealed an expected mean heterozygosity value of 0.54, indicating moderate genetic diversity among the tested okra accessions. Cluster analysis based on phenotypic and SSR markers differentiated the accessions into three distinct genetic groups. Wide phenotypic variation was observed for PH, FPL, NPPP, and PYPP under NS and DS conditions. PYPP was positively and significantly correlated with FPL (r = 0.81), ABG (r = 0.69), and HI (r = 0.67) under DS conditions, and FPL (r = 0.83) and AGB (r = 0.60) under NS conditions. Genetically complementary accessions such as LS04, LS05, LS06, LS07, LS08, LS10, LS11, LS15, LS18, LS23, LS24, and LS26 were identified for their high yield potential and related yield-improving traits under DS conditions. The identified accessions are recommended as parents for hybridization and selection programs to improve the yield potential of okra under drought-stressed environments.

Morpho-molecular diversity study of rice cultivars in Bangladesh

Rice is one of the frontline cereals in the world and the major cultivated crop in Bangladesh. A total of eleven simple sequence repeats (SSRs) and thirteen sequence-tagged site (STS) markers were used to characterize twenty-four rice cultivars in Bangladesh. Twenty-four markers generated 60 alleles with 2.5 alleles per locus. The average polymorphism information content (PIC) value was 0.40, while the mean value of heterozygosity, gene diversity, and major allele frequency were recorded as 0.10, 0.48 and 0.62, respectively. However, the SSR markers showed more specificity and a higher discrimination power than the STS markers. The cluster analysis displayed four major clusters with a genetic similarity coefficient value of 0.73. The morphological analyses of the grain identified that Binadhan-20 and BRRI dhan34 had the longest and the shortest seed size, respectively, with a variable correlation between the seed length, width and length/width ratio. The phenol reaction test distinguished seven cultivars as japonica and seventeen cultivars as indica or an intermediate type. All these results regarding the phenotypic data and marker information will be useful for parental selection in modern rice breeding programmes.

Molecular characterization using SSR markers and biochemical analysis of Moroccan and Spanish argan [Argania spinosa (L.) Skeels] ecotypes under water stress and rewatering

An integrated molecular and biochemical approach was carried out to compare Moroccan and Spanish argan [Argania spinosa (L.) Skeels] ecotypes. Genetic diversity of seedlings was evaluated using Simple Sequence Repeat (SSR) markers. In addition, water stress was imposed by holding water and enzymatic peroxidase (POX), superoxide dismutase (SOD), catalase (CAT) activities and total proteins in well-watered and water-deficient conditions were evaluated. The molecular characterization of the two ecotypes showed that the number of presumed alleles revealed by the SSR analysis ranged from 1 to 32 alleles per locus, with a mean value of 13 alleles and a mean heterozygosity value of 0.44. The assayed SSRs showed that most individuals were clustered according to their ecotype with a similar diversity level between Moroccan and Spanish ecotypes. Enzymatic activities in response to drought stress showed increase in POX and SOD activities for both ecotypes together with total protein content, but showed no significant differences in CAT activity. A potential tolerance to drought stress with increased levels of SOD activity in Spanish ecotypes grown in inland area of Alicante compared with Moroccan ecotypes grown in Essaouira, which is a coastal area, was also reported. In addition, the recovery period seemed to be sensed by argan plants as a new stress situation, as observed by the response of POX and CAT activities, suggesting an imbalance in the H2O2 metabolism. Our results suggestd an effect of geographic proximity and population isolation and/or breeding system on molecular phenotypes and responses to drought stress of the studied argan ecotypes. However, further investigations are needed to verify the induced differences.

Evaluating the genetic variability of rubber hybrid progenies of the two crosses PB260 x RO44/71 and PB260 x RO62/54 by RAPD technique

The agronomic values of this population have been evaluated in the field experiments based on their phenotypic performance of agronomic traits, but the genetic variability of this population needs to be evaluated via techniques based on genetic material - DNA. In this study, the genetic variability in the investigated population of 71 hybrids and their parents was evaluated by RAPD technique, using eight selected arbitrarily primers; Genetic parameters and dendrogram expressing the genetic relationships among the investigated population were analyzed by GenALEx 6.1, Popgene 1.31 and NTSYSpc 2.1 softwares. Eight primers were used to generate the amplify products on each individual in the investigated population. From 74 genotypes, a total of 109 fragments were generated, among which, there were 89 polymorphic bands representing 81.65% with an average of 11 polymorphic bands/primer. Genetic similarity coefficient among the investigated population, based on DICE coefficient, ranged from 0.560 (LH05/0822 and PB260) to 0.991 (LH05/0781 and LH05/0841) with an average of 0,796, meaning that the genetic distance among ranged from 0.009 to 0.440 with an average of 0.231. The Shannon index and mean heterozygosity values were 0.328 and 0,176, respectively. This indicated that the progenies of the two investigated crosses possessed a relatively high range of genetic variability. The analysis of molecular variance (AMOVA) showed that genetic variation within population represented 62%, while genetic variation among two different crosses contributes 38% to the total genetic variability. Dendrogram based on DICE’s genetic similarity using UPGMA method showed that the hybrids divide into two major genetic groups (0.75), but the crosses were scattered independently of the hybrid.

Assessment of OvineSNP50 in Nigerian and Kenyan sheep populations

Deciphering genomic information requires markers that are polymorphic and sufficient enough to capture its vast array of genetic data. Polymorphic loci can differ greatly between breeds of the same species and the exclusion of the Nigerian and some African sheep breeds during the development of the OvineSNP50 chip necessitated the validation of SNPs included on the chip to allow for genomic applications of the excluded breeds. A total of sixty sheep samples were genotyped [10 each of the Balami, Uda, West African Dwarf and Yankasa from Nigeria, Dorper and Red Maasai from Kenya (East Africa)] using the Ovine 50k Illumina SNP bead chip. Results revealed that 33,994 SNPs (97.47%) of the called 34,876 SNPs were validated for downstream analysis. Mean heterozygosity values of 0.154 and 0.153 were obtained for polymorphic SNPs on sex and autosomal chromosomes respectively, while the values of 0.662 and 0.054 were obtained on the sex and autosomal chromosomes respectively for the mean identity-bystate (IBS). Six and three individuals violated the per ID and identity-by-state (IBS) thresholds, respectively. It was observed that the Ovine 50k Illumina SNP bead chip was informative in the Nigerian and East African sheep that were studied, and should be useful in examining the underlying genetic variation. Keywords: Sheep, OvineSNP50, genome-wide, call rate, minor allele frequency

Evaluation of parasite and host genetics in two generations of a family with Chagas disease.

Chagas disease, caused by the protozoan Trypanosoma cruzi, is considered to be a multifactorial disease associated with host and parasite genetics, which influence clinical aspects of the disease and other host conditions. In order to understand better the evolution of the disease, this study intended to evaluation of parasite and host genetics in two generations of a family with Chagas disease from the Alto Paranaiba region, Minas Gerais, Brazil, comprising a mother and her five daughters. Several features were evaluated, including the characterization of T. cruzi directly from the blood of patients, host polymorphisms of genes related to cardiomyopathy (TNF, WISP1, CCR5, and TGF-β1) and clinical aspects of the patients. To verify the intraspecific variability of the parasite, the characterization was done directly from human blood using the PCR-LSSP technique and analyzed based on Dice coefficient and unweighted pair group analysis (UPGMA). The host polymorphism was evaluated by PCR-RFLP. The global results showed low variability of the parasites characterized from blood of patients, through Shannon index (0.492) and mean heterozygosity value per locus (0.322). All six patients presented the same genetic polymorphism profile for TNF, WISP1, and TGF-β1, and only one patient was homozygous to CCR5, which suggests that there is no association between the clinical aspects of the patients and their genetic profiles. In conclusion, the findings confirm that the understanding of the clinical evolution of Chagas disease goes beyond the genetic aspects of the parasite and the host.

Caracterizacion genetica de hibridos entre las especies Mytilus edulis platensis y Mytilus galloprovincialis (Mytilidae: Bivalvia) en la costa chilena

Given the hybridization ability between species Mytilus edulis platensis and M. galloprovincialis, this research proposed to assess the genetic variability of the hybrid offspring in relation to pure species, using 8 loci microsatellites. The study found differences between hybrid offspring comparing to pure species. The hybrid offspring had the highest observed mean heterozygosity values (Ho = 0,63 ± 0,28) and low values of inbreeding, which tend to significant deviations to negative values of (Fis), demonstrating excess of heterozygote in hybrids comparing with pure species, which displayed significant deviations towards positive values of Fis. The principal component analysis shows three distinct groups among the samples analyzed, identifying the hybrid offspring as an intermediate group between pure species.

Genetic Diversity of Maize (Zea mays L.) Genotypes Assessed by SSR Markers under Temperate Conditions

Genetic Diversity of Maize (Zea mays L.) Genotypes Assessed by SSR Markers under Temperate Conditions A set of twenty four maize lines comprising fifteen drought promising inbred lines, four drought susceptible inbred lines and five drought tolerant checks were analyzed for molecular characterization. These inbred lines belong to AICRP (All India Co-ordinated Research Programme) Maize Srinagar Centre and the checks were selected from CIMMYT (International Maize and Wheat Improvement Centre) material.. Molecular characterization was done using a set of 45 SSR markers having genome wide coverage. The marker data was analyzed using Power Marker Software (Version 3.25). The markers detected a total of 271 alleles with an average of 8.46 alleles per locus in twenty four maize lines. The average polymorphism information content (PIC) ranged from 0.56 and 0.89 with a mean of 0.78. The level of heterozygosity in the inbred panel was significantly low. The mean value of heterozygosity was 0.05 implying that most of the loci attained homozygosity. Dendrogram derived from UPGMA cluster analysis showed presence of two major clusters, one of which had many subgroups. Phenotyping of these inbreds was done by using morphological, maturity, physiological, yield and yield attributing traits. Genotyping data complemented by phenotyping data would be used to identify a number of pairwise combinations for the development of mapping populations for drought tolerance related traits and potential heterotic pairs for the development of drought tolerant hybrids...

Genetic diversity of some Iranian sweet cherry (Prunus avium) cultivars using microsatellite markers and morphological traits

The aim of this study was to characterize 23 important Iranian sweet cherry (Prunus avium) cultivars collected from different provinces of Iran and 1 foreign cultivar, which was used as control, considered for breeding programs by using 21 microsatellite markers and 27 morphological traits. In sweet cherry (Prunus avium) accessions, leaf, fruit, and stone morphological characters were evaluated during two consecutive years. The study revealed a high variability in the set of evaluated sweet cherry accessions. The majority of important correlations were determined among variables representing fruit and leaf size and variables related to color. Cluster analysis distinguished sweet cherry accessions into two distinct groups. Principal component analysis (PCA) of qualitative and quantitative morphological parameters explained over 86.59% of total variability in the first seven axes. In PCA, leaf traits such as leaf length and width, and fruit traits such as length, width, and weight, and fruit flesh and juice color were predominant in the first two components, indicating that they were useful for the assessment of sweet cherry germplasm characterization. Out of 21 SSR markers, 16 were polymorphic, producing 177 alleles that varied from 4 to 16 alleles (9.35 on average) with a mean heterozygosity value of 0.82 that produced successful amplifications and revealed DNA polymorphisms. Allele size varied from 95 to 290 bp. Cluster analyses showed that the studied sweet cherry genotypes were classified intofive main groups based mainly on their species characteristics and SSR data. In general, our results did not show a clear structuring of genetic variability within the Iranian diffusion area of sweet cherry, so it was not possible to draw any indications on regions of provenance delimitation. The results of this study contribute to a better understanding of sweet cherry genetic variations in Iran, thus making for more efficient programs aimed at preserving biodiversity and more rational planning of the management of reproductive material.

Evaluating the genetic impact of South and Southeast Asia on the peopling of Bangladesh.

Despite rapidly growing understandings and dependency on single nucleotide polymorphisms (SNPs), highly variable autosomal short tandem repeats (STRs) are still regarded as the most established method to differentiate individuals at forensic level. Here with large number of various ethnic groups we undertook this study to reveal the genetic structure of the most densely populated part of South Asia i.e. the Bangladesh. The purpose of this work was to estimate population parameters based on the allele frequencies obtained for 15 polymorphic autosomal STR loci investigated in caste and tribal populations from Bangladesh (n=706). We compared the results in a broader context by merging 24 different populations of Asia to pertain their affinity. Various statistical analyses suggested a clear cut demarcation of tribal and non-tribal in Bangladesh. Moreover, beside the phylogenetic structure of the studied populations, it is found that the mean heterozygosity value was highest among the populations of Bangladesh, likely because of gene flow from different directions. However, Tonchangya, Adi and Khumi showed sign of genetic isolation and reduced diversity, possibly as a result of genetic drift and/or strong founder effects working on small endogamous populations.

Genomic and Genotyping Characterization of Haplotype-Based Polymorphic Microsatellites in Prunus

Efficient utilization of microsatellites in genetic studies remains impeded largely due to the unknown status of their primer reliability, chromosomal location, and allele polymorphism. Discovery and characterization of microsatellite polymorphisms in a taxon will disclose the unknowns and gain new insights into the polymorphic alleles. In this study, we revealed the polymorphism status, primer categorization, chromosomal distribution, gene function, and genotyping performance of 319 haplotype-based polymorphic microsatellites (HPM) in expressed sequence tags (EST) of Prunus species, including peach, apricot, almond, plums, and cherries. Of the HPM, 262 are between two EST haplotypes and 57 are among three and more EST. In terms of species, 127 microsatellite polymorphisms are from different EST of peach, 108 from different EST between peach and other species, and 84fromdifferent EST between non-peach species. Based on the primer sequence alignments on the peach genome, there was one HPM per 678 kb and the 319 HPM were grouped into seven categories. The primers from the “deletion” category tended to yield higher allele numbers and polymorphism information content (PIC) values. Statistical analysis revealed the mean allele number, heterozygosity, PIC, and gene diversity value were all significantly higher in the HPM than in the haplotype-based non-polymorphic microsatellites (HNM), suggesting utilization of HPM markers could substantially increase the likelihood of allele polymorphism. Of the 234 unigenes annotated, 99 (42.3%) were categorized into binding function and 84 (35.9%) into catalytic activity, implying that these polymorphic alleles might have evolved primarily to play regulatory roles or catalyze enzymatic reactions.

New Interpretations about Clonal Architecture for the Sour Pitaya (<i>Stenocereus gummosus</i>, Cactaceae), Arising from Microsatellite Markers of <i>de novo</i> Isolation and Characterization

The use of molecular markers has improved the ecological and evolutionary research in the case of clonal reproduction species, allowing the identification of boundaries among clonal modules (ramets), genetic individuals (genets), and populations. Microsatellite markers were developed for Stenocereus gummosus, a columnar cactus with both sexual and clonal reproduction which is distributed in the Sonoran Desert, Mexico. 454-Pyrosequencing reads were analyzed to detect microsatellite markers. Forty primer pairs were screened to look for polymorphism. Nine loci were genotyped for two S. gummosus localities. Sampling strategy was intended to avoid collecting a genetic individual more than once, considering that clonal architecture for this cactus was previously deduced as clumped. Polymorphic loci exhibited low allele count, ranging from 2 - 7 (mean of 3.78 ± 0.62 SE); mean heterozygosity values were 0.221 and 0.234 HO and 0.408 and 0.306 HE, with FIS of 0.383 and 0.299, for peninsular and continental localities respectively. Unexpectedly, some multilocus genotypes were found repeated within locality, which were assumed as clones since data was evaluated as sufficient (clonal richness R of 0.966 and 0.897). These results were different from those previously reported: the distribution of clones might as well be intermingled, having a minimum ramet dispersion distance of 30 m. This characteristic was also consistent with the recent colonization proposed for this and other arid lands plants. A wider genetic neighborhood, due to clone dispersion might affect diversity indexes while increasing the chance of geitonogamy and mating among relatives. The markers isolation and its population characterization allowed addressing new questions about S. gummosus ecology, clonal reproduction and reproductive biology.

Microsatellite Analysis of Genetic Diversity Between Loach with Different Levels of Ploidy

We used microsatellite markers to investigate the genetic parameters of three different polyploidy populations of Misgurnus anguillicaudatus from Honghu City, Hubei Province. Polyacrylamide gel electrophoresis banding patterns of diploid (2n), triploid (3n) and tetraploid loaches (4n) were analyzed with PopGen software. A total of 68 alleles were obtained from seven microsatellite loci and the polymorphism information content (PIC) indices were all above 0.5. The average expected mean heterozygosity values (He) were 0.8420, 0.7186 and 0.8521; the average observed mean heterozygosity values (Ho) were 0.9674, 0.9785 and 0.8928; and the Hardy-Weinberg P values were 0.3078, 0.3151 and 0.3762, for diploid, triploid and tetraploid individuals, respectively. The results indicated that the three populations were highly polymorphic, with no deviations from Hardy-Weinberg equilibrium observed at all the seven microsatellite loci. This indicated a high level of genetic diversity within the populations. A cluster analysis diagram showed that the shortest genetic distance was between diploid and tetraploid loaches and they shared a close phylogenetic relationship. The triploid and tetraploid individuals had the most distant phylogenetic relationship.

Remarkably low genetic diversity and strong population structure in common bottlenose dolphins (Tursiops truncatus) from coastal waters of the Southwestern Atlantic Ocean

Knowledge about the ecology of bottlenose dolphins in the Southwestern Atlantic Ocean is scarce. Increased by-catch rates over the last decade in coastal waters of southern Brazil have raised concerns about the decline in abundance of local dolphin communities. Lack of relevant data, including information on population structure and connectivity, have hampered an assessment of the conservation status of bottlenose dolphin communities in this region. Here we combined analyses of 16 microsatellite loci and mitochondrial DNA (mtDNA) control region sequences to investigate genetic diversity, structure and connectivity in 124 biopsy samples collected over six communities of photographically identified coastal bottlenose dolphins in southern Brazil, Uruguay and central Argentina. Levels of nuclear genetic diversity were remarkably low (mean values of allelic diversity and heterozygosity across all loci were 3.6 and 0.21, respectively), a result that possibly reflects the small size of local dolphin communities. On a broad geographical scale, strong and significant genetic differentiation was found between bottlenose dolphins from southern Brazil–Uruguay (SB–U) and Bahia San Antonio (BSA), Argentina (AMOVA mtDNA ΦST = 0.43; nuclear FST = 0.46), with negligible contemporary gene flow detected based on Bayesian estimates. On a finer scale, moderate but significant differentiation (AMOVA mtDNA ΦST = 0.29; nuclear FST = 0.13) and asymmetric gene flow was detected between five neighbouring communities in SB–U. Based on the results we propose that BSA and SB–U represent two distinct evolutionarily significant units, and that communities from SB–U comprise five distinct Management Units (MUs). Under this scenario, conservation efforts should prioritize the areas in southern Brazil where dolphins from three MUs overlap in their home ranges and where by-catch rates are reportedly higher.

Genetic diversity inVicia fabaL. populations cultivated in Tunisia revealed by simple sequence repeat analysis

Faba bean (Vicia fabaL.) is one of the most important legumes in the world. Little is known about the genetic resources of faba bean in Southern Tunisia. In the present study, genetic diversity within Tunisian faba bean germplasms was investigated using 16 simple sequence repeat markers. In total, 50 alleles were detected. The number of alleles per marker ranged from 2 to 6, with an average of 3. Genetic diversity and polymorphism information content values averaged, respectively, 0.43 (range 0.34–0.51) and 0.36 (range 0.28–0.43). The mean heterozygosity value was 0.27. A model-based structure analysis based on neighbour-joining tree and factorial correspondence analysis revealed the presence of two subpopulations, consistent with the clustering based on genetic distance (GD). The overallFisvalue was 0.36, indicating the importance of selfing in these populations. Analysis of molecular variance revealed that the within-population genetic variance component was much higher than the between-population or between-subpopulation variance component. The genetic relationships based on Nei's GD revealed that AGD (Aguadulce) and SAG (Super Aguadulce) and TF1 and TF2 (Tafartassa-Gafsa) were the most closely related populations. Assessment of genetic variation within faba bean populations will be informative for the conservation of germplasms and the implementation of effective breeding programmes in Tunisia.

Genetic diversity and bottleneck studies in endangered Bhutia and Manipuri pony breeds

For studying the genetic diversity and bottleneck problem in Bhutia and Manipuri pony breeds of India, we analysed DNA samples of 34 Bhutia and 50 Manipuri, true to breed, ponies using 47 polymorphic microsatellite markers. All the microsatellites were observed to be highly polymorphic in nature in both Bhutia and Manipuri breeds with mean no. of alleles as 8.702±0.0493 and 8.416±0.0548 respectively. Genetic diversity values in terms of heterozygosity values within individual breeds were also high with very low inbreeding (Fis 0.102 and 0.055 in Bhutia and Manipuri ponies, respectively). Number of alleles in both the populations together ranged from 3 to 18 with an average of 10.851±1.583 per locus. The mean effective number of alleles was observed to 5.34±0.253. All loci except ASB017 and HTG004 showed high values of allele richness (>5.0). The mean observed and expected heterozygosities were 0.7159±0.022, 0.7986±0.011 (Levene's) and 0.7936±0.011 (Nei's), respectively. The high mean values of heterozygosity indicated the presence of high genetic diversity in both the pony populations. The overall mean value of within-population inbreeding estimates (Fis) was low (0.101±0.023) indicating low to moderate level of inbreeding. Bottleneck studies revealed that no recent bottleneck problem has taken place in both the populations. Both pony populations were found to be in mutation drift equilibrium. The study reveals that both the pony breeds have high diversity and timely action needs to be taken to conserve them.

Characterising the genetic diversity of Lithuanian sweet cherry (Prunus avium L.) cultivars using SSR markers

The polymorphisms and characteristics of microsatellite (SSR) loci from 31 sweet cherry (Prunus avium) cultivars were analysed. The cultivars were genotyped with 14 DNA primer pairs using a multiplex approach. A total of 20 unique alleles were identified in the Lithuanian cultivars that were absent in the cultivars of foreign origin. The analysis revealed that the expected and observed heterozygosities were higher in the cultivars of Lithuanian origin as compared with those that were introduced. Approximately 2–11 alleles (5.29 on average) with a mean heterozygosity value of 0.68 were established for microsatellite loci from the Lithuanian cultivars.Four distinct genetic groups of cultivars were defined using cluster analysis. One cluster consisted of Lithuanian landraces, Russian cultivars and their hybrids. The earliest (first generation) Lithuanian cultivars, derived from Lithuanian landraces and Russian cultivars also fitted this cluster. Another cluster consisted of the second generation of cultivars of Lithuanian, Ukrainian and Belarusian origin. The most recent cultivars of Lithuanian origin and the cultivars from Canada and Western Europe were grouped into a different cluster. Fourth cluster consisted of three cultivars: Belobokaya rannaya; its progeny, Meda; and Irema BS of unknown origin.Characterising the genetic backgrounds of the cultivars revealed the unique features of the sweet cherry grown in the region.

Analysis of genetic variability in Aristaeomorpha foliacea (Crustacea, Aristeidae) using DNA-ISSR (Inter Simple Sequence Repeats) markers

This work reports the first genetic data of Aristaeomorpha foliacea, a marine decapod of high commercial value, from six Mediterranean localities and one new fishing ground in the Mozambique Channel. The use of five Inter Simple Sequence Repeat (ISSR) primers provided 150 polymorphic loci. Average estimates of genetic diversity did not significantly differ among sampled localities, with a mean value of heterozygosity H = 0.105 ± 0.015. Analysis of molecular variance (AMOVA) allocated > 98% of genetic variability to the within-sample component, displaying values higher than those previously reported in ISSR studies on marine invertebrates. Cluster analyses did not detect geographically or genetically distinct groups. The observed lack of large-scale genetic differentiation is discussed in relation to the high potential for larval dispersal of the species and to features of the marker employed.

Transferability of non-genic microsatellite and gene-based sunflower markers to safflower

Safflower (Carthamus tinctorius L.) DNA marker resources are currently very limited. The objective of this study was to determine the feasibility of transferring non-genic microsatellite (SSR) markers and gene-based markers, including intron fragment length polymorphism (IFLP) and resistance gene candidates (RGC)-based markers from sunflower (Helianthus annuus L.) to safflower, both species belonging to the Asteraceae family. Cross-species amplification of 119 non-genic SSRs, 48 IFLPs, and 19 RGC-based sunflower markers in 22 lines and germplasm accessions of safflower was evaluated. Additionally, 69 EST-SSR markers previously reported to amplify in safflower were tested. The results showed that 17.6% of the non-genic SSR, 56.2% of the IFLP, and 73.7% of the RGC-based markers were transferable to safflower. The percentage of transferable markers showing polymorphic loci was 66.6% for non-genic SSR, 70.6% for EST-SSR, 55.5% for IFLP, and 71.4% for RGC-based markers. The highest polymorphism levels were found for non-genic SSR. The average number of alleles per polymorphic locus and mean heterozygosity values were 2.9 and 0.46, respectively, for non-genic SSR, 2.2 and 0.35 for EST-SSR, 2.1 and 0.24 for IFLP, and 2.0 and 0.34 for RGC-based markers. The results of this study revealed a low rate of transferability for non-genic SSR sunflower markers and a better rate of transferability for IFLP and RGC-based markers. Transferable genic and non-genic sunflower markers can have utility for trait and comparative mapping studies in safflower.