Abstract:A little is known about the genetic variability present in globe artichoke, cultivated and wild cardoons. This knowledge is very important for efficient genetic resources utilization, and to gain a better understanding of genetic structure of this botanical varieties. With the aims to determine genetic distances between Cynara cardunculus accessions and to compare two molecular markers systems for their efficiency to differ between botanical varieties, a molecular characterization of sixteen accessions from di… Show more
“…Wild cardoon SSR polymorphism showed that all populations were clearly distinguished from each other suggesting high performance of the SSR as molecular tools for genetic identification. Similar studies using microsatellites to analyze populations of Cynara showed high levels of polymorphism (Casadevall et al, 2011;Gatto et al, 2013). Overall, the results of molecular markers analysis revealed a high gene diversity of wild cardoon populations (He = 0.77) and supported those found by Khaldi et al (2012) for Tunisian wild cardoon genotypes.…”
“…Wild cardoon SSR polymorphism showed that all populations were clearly distinguished from each other suggesting high performance of the SSR as molecular tools for genetic identification. Similar studies using microsatellites to analyze populations of Cynara showed high levels of polymorphism (Casadevall et al, 2011;Gatto et al, 2013). Overall, the results of molecular markers analysis revealed a high gene diversity of wild cardoon populations (He = 0.77) and supported those found by Khaldi et al (2012) for Tunisian wild cardoon genotypes.…”
“…Moreover, the electrophoresis in agarose gel used in SRAP markers is faster and less laborious than the electrophoresis in polyacrylamide gel for microsatellites. On the other hand, Casadevall et al (2011), using microsatellites and SRAP markers to study the genetic diversity of Cynara cardunculus, recommended to use microsatellite markers for their easy visualization and codominance information. The fact that in this study as well as in our research (Table 6) the estimators of genetic diversity obtained by SRAP appear lower than those obtained by microsatellite might be due to the characteristics of the marker system.…”
Peru is an important producer of specialty coffee beans in the world, however the genetic of their coffee plant populations is unknown. Therefore, the genetic diversity and population structure of a Peruvian germplasm collection of plant coffee was analyzed to ascertain its potential use in plant breeding and conservation. In this work 54 DNA genotypes from 17 Coffea arabica L. and one C. canephora Pierre ex A. Froehner accessions were analyzed by microsatellite and sequence-related amplified polymorphism (SRAP) markers. In the assessment of molecular markers both systems were adequate to perform C. arabica germplasm collection genetic analysis. The obtained genetic diversity estimators were similar to germplasm assessments from other plant breeding programs. In the population structure analysis, the genetic differentiation (GST = 0.6584) and genetic flow (Nm = 0.2594) estimators were high. In analysis of molecular variance (AMOVA), total variation was divided 43.05% between accessions and 56.95% within accessions. In the Bayesian analysis with STRUCTURE software using admixed model for K = 2, the C. arabica and C. canephora accessions were separated, while for K = 7, the C. arabica accessions were grouped similarly to what obtained by the unweighted pair group method with arithmetic mean (UPGMA) dendrogram. The high genetic differentiation and genetic structuring of the accessions would indicate that the cultivars, from which the accessions were originated, have been preserved over time. The genetic diversity of Peruvian coffee might be the consequence of a long history of introductions of cultivars from different origins.
“…In previous studies (Cravero, Martin and Cointry, 2007;Casadevall, Martin and Cravero, 2011), the variability available between some accessions, belonging to the local C. cardunculus collection, was evaluated using Sequence Related Amplified Polymorphism (SRAP) (Li and Quiros, 2001). Those studies proved that SRAP is also a helpful tool to detect genetic diversity in this species and to classify accessions into groups based on their genetic distance values.…”
This study was carried out in order to compare different methodologies to select a representative core collection from an initial collection of Cynara cardunculus L. species, using both morphological and molecular markers. The combination of two stratification criteria with three sampling strategies allowed the establishment of six different core collections. The Maximization strategy was applied in order to obtain the seventh one. All the obtained collections were validated through phenotypic and molecular parameters, establishing as an initial criterion that the core collection should include, at most, 35-40 % of the accessions belonging to the original collection. All collections passed molecular validation; nevertheless morphological validation determined that the Proportional sampling strategy is the best to keep the initial variability while retaining the least number of accessions, especially when combined with the first stratification criterion. Although Maximization strategy allowed to preserve the original variability, it retained the largest number of accessions. In conclusion, the combination PrS1 (proportional sampling and first stratification criterion) is the best strategy to perform a representative core collection from a Cynara cardunculus L. initial collection, using both morphological and molecular data.
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