Genetic diversity among varieties and wild species accessions of pea (Pisum sativum L.) based on molecular markers, and morphological and physiological characters

Genome ◽  
2005 ◽  
Vol 48 (2) ◽  
pp. 257-272 ◽  
Author(s):  
B Tar'an ◽  
C Zhang ◽  
T Warkentin ◽  
A Tullu ◽  
A Vandenberg
Keyword(s):  
Genetic Diversity ◽  
Cluster Analysis ◽  
Molecular Markers ◽  
Pisum Sativum ◽  
Simple Sequence Repeat ◽  
Sequence Repeat ◽  
Agronomic Characters ◽  
Breeding Programs ◽  
Pisum Sativum L ◽  
Simple Sequence

Random amplified polymorphic DNA, simple sequence repeat, and inter-simple sequence repeat markers were used to estimate the genetic relations among 65 pea varieties (Pisum sativum L.) and 21 accessions from wild Pisum subspecies (subsp.) abyssinicum, asiaticum, elatius, transcaucasicum, and var. arvense. Fifty-one of these varieties are currently available for growers in western Canada. Nei and Li's genetic similarity (GS) estimates calculated using the marker data showed that pair-wise comparison values among the 65 varieties ranged from 0.34 to 1.00. GS analysis on varieties grouped according to their originating breeding programs demonstrated that different levels of diversity were maintained at different breeding programs. Unweighted pair-group method arithmetic average cluster analysis and principal coordinate analysis on the marker-based GS grouped the cultivated varieties separately from the wild accessions. The majority of the food and feed varieties were grouped separately from the silage and specialty varieties, regardless of the originating breeding programs. The analysis also revealed some genetically distinct varieties such as Croma, CDC Handel, 1096M-8, and CDC Acer. The relations among the cultivated varieties, as revealed by molecular-marker-based GS, were not significantly correlated with those based on the agronomic characters, suggesting that the 2 systems give different estimates of genetic relations among the varieties. However, on a smaller scale, a consistent subcluster of genotypes was identified on the basis of agronomic characters and their marker-based GS. Furthermore, a number of variety-specific markers were identified in the current study, which could be useful for variety identification. Breeding strategies to maintain or enhance the genetic diversity of future varieties are proposed.Key words: Pisum sativum, molecular markers, genetic relationships, cluster analysis.

Genetic diversity studies in pea (Pisum sativum L.) using simple sequence repeat markers

2013 ◽  
Vol 12 (3) ◽  
pp. 3540-3550 ◽  
Author(s):  
P. Kumari ◽  
N. Basal ◽  
A.K. Singh ◽  
V.P. Rai ◽  
C.P. Srivastava ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Pisum Sativum ◽  
Simple Sequence Repeat ◽  
Sequence Repeat ◽  
Simple Sequence Repeat Markers ◽  
Pisum Sativum L ◽  
Diversity Studies ◽  
Simple Sequence

scholarly journals Evaluation and Pre-selection of New Grapevine Genotypes Resistant to Downy and Powdery Mildew, Obtained by Cross-Breeding Programs in Spain

2021 ◽  
Vol 12 ◽  
Author(s):  
Leonor Ruiz-García ◽  
Pilar Gago ◽  
Celia Martínez-Mora ◽  
José Luis Santiago ◽  
Diego J. Fernádez-López ◽  
...  
Keyword(s):  
Molecular Markers ◽  
Powdery Mildew ◽  
Simple Sequence Repeat ◽  
Selection Process ◽  
Sequence Repeat ◽  
Sources Of Resistance ◽  
Breeding Programs ◽  
Phenotypic Resistance ◽  
Simple Sequence ◽  
Selection Of

The need to develop an environmentally friendly, sustainable viticulture model has led to numerous grapevine improvement programmes aiming to increase resistance to downy and powdery mildew. The success of such programmes relies on the availability of protocols that can quantify the resistance/susceptibility of new genotypes, and on the existence of molecular markers of resistance loci that can aid in the selection process. The present work assesses the degree of phenotypic resistance/susceptibility to downy and powdery mildew of 28 new genotypes obtained from crosses between “Monastrell” and “Regent.” Three genotypes showed strong combined resistance, making them good candidates for future crosses with other sources of resistance to these diseases (pyramiding). In general, laboratory and glasshouse assessments of resistance at the phenotype level agreed with the resistance expected from the presence of resistance-associated alleles of simple sequence repeat (SSR) markers for the loci Rpv3 and Ren3 (inherited from “Regent”), confirming their usefulness as indicators of likely resistance to downy and powdery mildew, respectively, particularly so for downy mildew.

scholarly journals Genetic diversity in Jatropha species from different regions of Brazil based on morphological characters and inters-simple sequence repeat (ISSR) molecular markers

2015 ◽  
Vol 14 (25) ◽  
pp. 2066-2079 ◽  
Author(s):  
Silva Rosa Pazeto Mariana ◽  
Helena Uneda Trevisoli Sandra ◽  
Arcenio Pimentel Correa Aretha ◽  
Formice Vianna Viviane ◽  
Carvalho Leite Daniel ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Molecular Markers ◽  
Simple Sequence Repeat ◽  
Morphological Characters ◽  
Sequence Repeat ◽  
Issr Molecular Markers ◽  
Simple Sequence

scholarly journals Characterisation and genetic diversity analysis of selected chickpea cultivars of nine countries using simple sequence repeat (SSR) markers

2011 ◽  
Vol 62 (2) ◽  
pp. 177 ◽  
Author(s):  
Tadesse Sefera ◽  
Bekele Abebie ◽  
Pooran M. Gaur ◽  
Kebebew Assefa ◽  
Rajeev K. Varshney
Keyword(s):  
Genetic Diversity ◽  
Ssr Markers ◽  
Simple Sequence Repeat ◽  
Dna Fingerprint ◽  
Pedigree Information ◽  
Sequence Repeat ◽  
Dissimilarity Matrix ◽  
Breeding Programs ◽  
Simple Sequence ◽  
Chickpea Cultivars

The genomic DNA profiles of 48 chickpea cultivars released in nine countries and of historical significance to the chickpea breeding programs at ICRISAT and in Ethiopia were evaluated using 48 simple sequence repeat (SSR) markers. Across the cultivars, a total of 504 alleles representing the 48 SSR loci were detected with frequencies ranging from three to 22 (mean 10.5) alleles per locus. The polymorphism information content (PIC) for the SSR markers varied from 0.37 to 0.91 (mean 0.77). A subset of only three highly informative SSR markers (TA176, TA2, TA180) enabled complete discrimination among all 48 chickpea cultivars tested. Hierarchical neighbour-joining UPGMA cluster analysis based on simple matching dissimilarity matrix resolved the 48 cultivars into two major clusters representing desi and kabuli types. These cluster groupings of the cultivars were consistent with the pedigree information available for the cultivars as to the phenotypic classes of chickpea types. Analysis of the temporal patterns of the SSR diversity by classifying 48 chickpea cultivars into four periods of release revealed increasing tendencies in the overall genetic diversity from 0.42 for the earliest varieties developed in the 1970s to 0.62 for those released in the 1980s, and reached a maximum and equivalent level of 0.72 for the varieties developed in the 1990s and 2000s. Overall, the study ascertained that SSRs provide powerful marker tools in revealing genetic diversity and relationships in chickpeas, thereby proving useful for selection of parents in breeding programs and also for DNA fingerprint identification of cultivars.

scholarly journals Genetic Diversity of Arabica Coffee (Coffea arabicaL.) in Nicaragua as Estimated by Simple Sequence Repeat Markers

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Mulatu Geleta ◽  
Isabel Herrera ◽  
Arnulfo Monzón ◽  
Tomas Bryngelsson
Keyword(s):  
Genetic Diversity ◽  
Genetic Variation ◽  
Simple Sequence Repeat ◽  
Significant Contribution ◽  
Gene Diversity ◽  
Ex Situ ◽  
Sequence Repeat ◽  
Breeding Programs ◽  
Arabica Coffee ◽  
Simple Sequence

Coffea arabicaL. (arabica coffee), the only tetraploid species in the genusCoffea, represents the majority of the world’s coffee production and has a significant contribution to Nicaragua’s economy. The present paper was conducted to determine the genetic diversity of arabica coffee in Nicaragua for its conservation and breeding values. Twenty-six populations that represent eight varieties in Nicaragua were investigated using simple sequence repeat (SSR) markers. A total of 24 alleles were obtained from the 12 loci investigated across 260 individual plants. The total Nei’s gene diversity (HT) and the within-population gene diversity (HS) were 0.35 and 0.29, respectively, which is comparable with that previously reported from other countries and regions. Among the varieties, the highest diversity was recorded in the variety Catimor. Analysis of variance (AMOVA) revealed that about 87% of the total genetic variation was found within populations and the remaining 13% differentiate the populations (FST=0.13;P<0.001). The variation among the varieties was also significant. The genetic variation in Nicaraguan coffee is significant enough to be used in the breeding programs, and most of this variation can be conserved throughex situconservation of a low number of populations from each variety.

scholarly journals KARAKTERISASI KERAGAMAN GENETIK 27 GENOTIPE CABAI BERDASARKAN MARKA SSR (SIMPLE SEQUENCE REPEAT)

2018 ◽  
Vol 17 (2) ◽  
Author(s):  
Rerenstradika Tizar Terryana ◽  
Kristianto Nugroho ◽  
Habib Rijzaani ◽  
Puji Lestari
Keyword(s):  
Genetic Diversity ◽  
Cluster Analysis ◽  
Ssr Markers ◽  
Simple Sequence Repeat ◽  
Chili Pepper ◽  
Sequence Repeat ◽  
Average Value ◽  
Allele Number ◽  
Principle Coordinate Analysis ◽  
Simple Sequence

Chili pepper (Capsicum annuum) is one of the high economical horticultural comodity in Indonesia and its genetic diversity contributes to the success of breeding programs. Simple sequence repeat (SSR) markers can be used to analyze genetic diversity among chili pepper genotypes. The aim of this research was to analyze the genetic diversity of twenty-seven genotypes of chili pepper by using 24 SSR markers. The collected data was analyzed using cluster analysis and principle coordinate analysis (PCoA). The result showed that high allele variation (4–17 alleles) was observed among chili pepper genotypes tested, with an average allele number and Polymorphism Information Content (PIC) value was 7.708 and 0.758 (0.598–0.920) respectively. All of SSR markers showed PIC value >0.5 which indicated that these markers were suitable for chili pepper diversity studies with a high differentiation and with the average value of genetic diversity was 0.78. The clustering and principle coordinate analysis showed that twenty-seven genotypes of chili pepper were divided into two groups (coefficient of similarity 0.74 in cluster analysis) indicating a high genetic variability among them. Genetic diversity analysis in this study will be useful as an initial basis of selection for appropriate parents with desired traits to assist the breeding program of chili pepper in Indonesia.

scholarly journals Microsatellite Markers and Genetic Diversity in Japanese Apricot (Prunus mume)

HortScience ◽  
2004 ◽  
Vol 39 (7) ◽  
pp. 1571-1574 ◽  
Author(s):  
Zhi-Hong Gao ◽  
Zhi-Jun Shen ◽  
Zhen-Hai Han ◽  
Jing-Gui Fang ◽  
Yu-Ming Zhang ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Cluster Analysis ◽  
Genetic Distance ◽  
Microsatellite Locus ◽  
Simple Sequence Repeat ◽  
Prunus Mume ◽  
Sequence Repeat ◽  
Microsatellite Sequence ◽  
Japanese Apricot ◽  
Simple Sequence

Sequencing amplification fragments produced using simple-sequence repeat (SSR) primer pairs pchgms2 and UDP96008 in `Dayezhugan' japanese apricot showed that SSRs obtained included a microsatellite locus originally identified in peach. The microsatellite sequence homogeneity between UDP96008 in japanese apricot in this study and UDP96008 in the peach in GenBank was 98%. Twenty-four japanese apricot genotypes originating in diverse geographic areas had been identified with 14 SSR primer pairs developed in different species of Prunus. In total, 129 alleles were obtained and per primer pairs detected 2.5 alleles on the average. The results from cluster analysis showed that the genetic distance between `Nanhong' and `Zhonghong' was the closest, and cultivars from China and from Japan could not be separated completely.

scholarly journals Genetic Diversity Assessment of Selected Annona muricata L. Germplasm in Sri Lanka

2020 ◽  
pp. 1-13
Author(s):  
S. H. M. R. N. P. Samaradiwakara ◽  
W. L. G. Samarasinghe ◽  
P. G. S. Shantha ◽  
K. G. C. N. Jayarathna ◽  
P. Dehigaspitiya ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Sri Lanka ◽  
Simple Sequence Repeat ◽  
Inter Simple Sequence Repeat ◽  
Issr Markers ◽  
Polymorphic Band ◽  
Annona Muricata ◽  
Sequence Repeat ◽  
Breeding Programs ◽  
Simple Sequence

Annona muricata L. commonly known as soursop is an underutilized fruit crop species in Sri Lanka gaining much importance in the recent past due to its high nutritional and medicinal value. Soursop germplasm collections are available within the country and assessing the genetic diversity is needed to proceed with conservation, detecting promising lines and breeding programs. This study was conducted to assess the genetic diversity of 50 soursop individuals using Inter-Simple Sequence Repeat (ISSR) markers. The study was conducted at Plant Genetic Resources Centre of the Department of Agriculture in Gannoruwa during 2017 to 2019. DNA of the 50 soursop samples were extracted using CTAB method and Polymerase Chain Reaction (PCR) was carried using 13 Inter Simple Sequence Repeat (ISSR) Markers. PCR products were visualized using 1.5 percent Agarose gel electrophoresis under the Biorad Gel documentation system and analyzed using POPGENE 1.31. PCR amplified 139 bands from 13 ISSR markers among which 118 were found to be polymorphic. The polymorphic band percentage was 85 percent while as the average number of bands observed (Na) was 1.8489 and the effective allele number (Ne) was 1.5377. The Nei's gene diversity index (h) was 0.3079. The Shannon Information Index (I) found to be 0.4556. Dendrogram constructed based on the UPGMA method clustered the studied accessions into four major clusters at 80 percent similarity level. Results revealed considerable degree of genetic diversity existed within the studied soursop germplasms at Sri Lanka. Existing genetic diversity within soursop individuals will serve as germplasm bank to identify and utilize potential germplasm resources for conservation and future breeding programs to develop quality soursop varieties in Sri Lanka.

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