scholarly journals Analysis of Genetic Relationships of Calathea Species and Cultivars by AFLP Markers

HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 888A-888
Author(s):  
Jianjun Chen* ◽  
Richard Henny ◽  
C. Thomas Chao ◽  
Pachanoor Devanand

Calathea, the largest genus in the family Marantaceae, is composed of 100 species native to tropical America in moist or swampy forest habitats. Because of their brilliant patterns of leaf color and different textures plus ability to tolerate low light levels, calatheas have been widely produced as ornamental foliage plants for interiorscaping. Thus far, genetic relationships among its species and cultivars have not been documented. This study analyzed the relationships of 34 cultivars across 14 species using amplified fragment length polymorphism (AFLP) markers. Six EcoR I + 2/Mse I + 3 primer set combinations were used in this investigation. Each selected primer set generated 105 to 136 scorable fragments. A total of 733 AFLP fragments were detected of which 497 were polymorphic (68%). A dendrogram was constructed using the unweighted pair-group method of arithmetic averages (UP-GMA) technique and a principal coordinated analysis (PCOA) was used to analyze the relationships. The 34 cultivars were divided into four clusters. Cluster I had 19 cultivars derived from C. roseo-picta and C. loesnerii with Jaccard's similarity coefficients from 0.74 to 0.97, of which six are somaclonal variants or sports and two cultivars are genetic identical. Only C. kennedeae `Helen' is positioned in cluster II. Cluster III had 10 cultivars across seven species; Jaccard's similarity coefficients among them varied from 0.41 to 0.63. Four species were situated in cluster IV with Jaccard's similarity between 0.27 to 0.41. Results from this study indicate that broadening of genetic diversity is needed for cultivars in cluster I as they are the most commonly grown calatheas but genetically are very close.

2004 ◽  
Vol 129 (5) ◽  
pp. 690-697 ◽  
Author(s):  
Pachanoor S. Devanand ◽  
Jianjun Chen ◽  
Richard J. Henny ◽  
Chih-Cheng T. Chao

Philodendrons (Philodendron Schott) are among the most popular tropical ornamental foliage plants used for interior decoration. However, limited information is available on the genetic relationships among popular Philodendron species and cultivars. This study analyzed genetic similarity of 43 cultivars across 15 species using amplified fragment length polymorphism (AFLP) markers with near infrared fluorescence labeled primers. Forty-eight EcoR I + 2/Mse I + 3 primer set combinations were screened, from which six primer sets were selected and used in this investigation. Each selected primer set generated 96 to 130 scorable fragments. A total of 664 AFLP fragments were detected, of which 424 (64%) were polymorphic. All cultivars were clearly differentiated by their AFLP fingerprints, and the relationships were analyzed using the unweighted pair-group method of arithmetic average cluster analysis (UPGMA) and principal coordinated analysis (PCA). The 43 cultivars were divided into five clusters. Cluster I comprises eight cultivars with arborescent growth style. Cluster II has only one cultivar, `Goeldii'. There are 16 cultivars in cluster III, and most of them are self-heading interspecific hybrids originated from R.H. McColley's breeding program in Apopka, Fla. Cluster IV contains 13 cultivars that exhibit semi-vining growth style. Cluster V has five cultivars that are true vining in morphology, and they have lowest genetic similarity with philodendrons in other clusters. Cultivated philodendrons are generally genetically diverse except the self-heading hybrids in cluster III that were mainly developed using self-heading and semi-vining species as parents. Seven hybrid cultivars have Jaccard's similarity coefficients of 0.88 or higher, suggesting that future hybrid development needs to select parents with diverse genetic backgrounds.


Genome ◽  
2002 ◽  
Vol 45 (6) ◽  
pp. 1175-1180 ◽  
Author(s):  
F J Massawe ◽  
M Dickinson ◽  
J A Roberts ◽  
S N Azam-Ali

Bambara groundnut (Vigna subterranea (L.) Verdc), an African indigenous legume, is popular in most parts of Africa. The present study was undertaken to establish genetic relationships among 16 cultivated bambara groundnut landraces using fluorescence-based amplified fragment length polymorphism (AFLP) markers. Seven selective primer combinations generated 504 amplification products, ranging from 50 to 400 bp. Several landrace-specific products were identified that could be effectively used to produce landrace-specific markers for identification purposes. On average, each primer combination generated 72 amplified products that were detectable by an ABI Prism 310 DNA sequencer. The polymorphisms obtained ranged from 68.0 to 98.0%, with an average of 84.0%. The primer pairs M-ACA + P-GCC and M-ACA + P-GGA produced more polymorphic fragments than any other primer pairs and were better at differentiating landraces. The dendrogram generated by the UPGMA (unweighted pair-group method with arithmetic averaging) grouped 16 landraces into 3 clusters, mainly according to their place of collection or geographic origin. DipC1995 and Malawi5 were the most genetically related landraces. AFLP analysis provided sufficient polymorphism to determine the amount of genetic diversity and to establish genetic relationships in bambara groundnut landraces. The results will help in the formulation of marker-assisted breeding in bambara groundnut.Key words: under-utilized, African legume, molecular markers.


2004 ◽  
Vol 2 (3) ◽  
pp. 189-198 ◽  
Author(s):  
Jasmina Muminović ◽  
Albrecht E. Melchinger ◽  
Thomas Lübberstedt

Genetic relationships among elite celeriac varieties and celeriac accessions conserved in genebanks are generally unknown. The objective of this study was to use amplified fragment length polymorphism (AFLP) markers and morphological characterization to identify material that could be of use in celeriac breeding. Genetic relationships were estimated in 34 elite celeriac varieties bred in Europe and 28 celeriac accessions conserved at the German genebank. Two varieties of celery, two varieties of leaf celery and three genebank accessions of wildApiumspecies were additionally analysed. FifteenEcoRI/MseI-based AFLP primer combinations were used. Polymorphic AFLP fragments were scored for calculation of Jaccard's coefficient of genetic similarity (GS). Morphological distances (MD) were determined based on 11 morphological traits. Average GS estimate in elite germplasm (GS=0.90) was higher than in exotic germplasm (GS=0.80). An AMOVA (analysis of molecular variance) revealed that a high proportion of variation was due to variation within elite celeriac varieties and genebank accessions. Although GS and MD matrices were poorly correlated (r=0.22), UPGMA (unweighted pair group method using arithmetic averages) cluster analyses revealed clear genetic groupings of celeriac germplasm, which was supported by morphological traits. Elite, moderately bred and exotic varieties formed distinct clusters, indicating that only a part of the available genetic diversity in celeriac germplasm has been exploited in breeding. DistinctApiumspecies might be useful for the introgression of new genes into cultivated celeriac material. Broadening of celeriac collections in genebanks and detection of new genetic resources are vital for improvements in celeriac breeding.


Genome ◽  
2000 ◽  
Vol 43 (6) ◽  
pp. 975-980 ◽  
Author(s):  
M S Negi ◽  
A Singh ◽  
M Lakshmikumaran

Withania somnifera is an important medicinal plant, and its anticancerous properties have been attributed to various classes of withanolide compounds. The objective of the present study was to investigate the inter- and intraspecific genetic variation present in 35 individuals of W. somnifera and 5 individuals of W. coagulans using AFLP (amplified fragment length polymorphism) marker technique. The information about genetic variation determined from AFLP data for 40 individuals was employed to estimate similarity matrix value based on Jaccard's coefficient. The similarity values were further used to construct a phenetic dendrogram revealing the genetic relationships. The dendrogram generated by UPGMA (unweighted pair group method of arithmetic averages) distinguished W. somnifera from W. coagulans and formed two major clusters. These two main clusters shared a similarity coefficient of 0.3, correlating with the high level of polymorphism detected. The dendrogram further separated W. somnifera into three subclasses corresponding to Kashmiri and Nagori groups and an intermediate type. The AFLP profile of Kashmiri individuals was distinct from that of the Nagori group of plants. The intermediate genotype was distinct as it shared bands with both the Kashmiri and Nagori individuals, even though it was identified as a Kashmiri morphotype. Furthermore, the intermediate type shared a similarity coefficient of 0.8 with the Kashmiri individuals. The present work revealed low levels of variation within a population though high levels of polymorphism were detected between Nagori and Kashmiri populations. The ability of AFLP markers for efficient and rapid detection of genetic variations at the species as well as intraspecific level qualifies it as an efficient tool for estimating genetic similarity in plant species and effective management of genetic resources.Key words: Withania, AFLP, genetic variation, phenetic relationships, medicinal plant.


2016 ◽  
Vol 44 (2) ◽  
pp. 557-562
Author(s):  
Ebru SAKAR ◽  
Hulya UNVER ◽  
Mehmet ULAS ◽  
Biljana LAZOVIC ◽  
Sezai ERCISLI

Olive and olive oil have a prominent place in the cultures of the countries within the Mediterranean basin including Turkey. The genetic relationships among 30 olive (Olea europaea L.) genotypes sampled from Gaziantep province in Turkey were examined using 10 simple sequence repeat (SSR) markers (DCA9, DCA11, DCA15, DCA18UDO4, UDO9, UDO11, UDO12, UDO22, UDO24). Also, three well known Turkish and one foreign olive cultivar were also included within the SSR analysis. The number of alleles per locus of the SSR markers ranged from 5 (DCA15, UDO9) to 14 (DCA9) (average 7.9), for a total of 79 alleles. Similarity coefficients were calculated on the basis of 79 amplified bands. A dendrogram was created according to the 10 SSR markers by the unweighted pair-group method. The banding patterns obtained from the SSR primers allowed all of the genotypes/cultivars to be distinguished. According to the dendrogram, the 33 olive genotypes and cultivars were clustered into five main clusters. The most closely related genotypes were 'Oguzeli 3' and 'Yavuzeli 1' with 0.80 similarity ratio. The most genetically divergent cultivars were 'Yavuzeli 6' and 'Kilis Yaglik' (0.30), 'Yavuzeli 6' and 'Saurani' (0.20), 'Nizip 7' and 'Yavuzeli 4' (0.15), 'Islahiye 5' and 'Nizip Yaglik' (0.10). In conclusion, SSR analysis can be an efficient method for olive genotypes and cultivar identification and can offer valuable informative data to identify olive genotypes and cultivars grown in Turkey.


HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 861C-861 ◽  
Author(s):  
Pachanoor S. Devanand ◽  
C. Thomas Chao* ◽  
Jianjn Chen ◽  
Richard J. Henny

Anthurium is the largest genus in the family Araceae, consisting of about 1000 species. Anthuriums are valued for their colorful spathes and traditionally used as cut flowers. With the introduction of compact cultivars through breeding, a series of container-grown cultivars have been released and widely produced as flowering foliage plants. However, limited information is available about genetic relatedness among these container-grown cultivars. This study analyzed genetic relationships of 58 cultivars using amplified fragment length polymorphism (AFLP) markers with near infrared fluorescence labeled primers. Forty-eight EcoR I + 2/Mse I + 3 primer set combinations were screened from which six primer sets were selected and used in this investigation. Each selected primer set generated 94 to 115 scorable fragments. A total of 647 AFLP fragments were detected of which 401 were polymorphic (67%). All cultivars were clearly differentiated by their AFLP finger-prints. A dendrogram was constructed using the unweighted pair-group method of arithmetic averages (UPGMA) technique and a principal coordinated analysis (PCA) was used to analyze the relationships. The 58 cultivars were divided into three clusters; clusters I, II, and III had 40, 10, and 8 cultivars, respectively. Most commonly grown cultivars were positioned in cluster I, where had Jaccard similarity coefficients among them ranged from 0.7 to 0.98. Eighteen of the 40 shared Jaccard similarity coefficient of 0.8 or higher, indicating that genetic diversity for cultivated container-grown Anthurium is needed.


Genome ◽  
2004 ◽  
Vol 47 (3) ◽  
pp. 510-518 ◽  
Author(s):  
Young Hoon Park ◽  
Marilyn A.L West ◽  
Dina A St. Clair

Cultivated tomato (L. esculentum L.) germplasm exhibits limited genetic variation compared with wild Lycopersicon species. Amplified fragment length polymorphism (AFLP) markers were used to evaluate genetic variation among 74 cultivars, primarily from California, and to fingerprint germplasm to determine if cultivar-specific patterns could be obtained. All 74 cultivars were genotyped using 26 AFLP primer combinations; of the 1092 bands scored, 102 AFLP bands (9.3%) were polymorphic. Pair-wise genetic similarity coefficients (Jaccard and Nei–Li) were calculated. Jaccard coefficients varied from 0.16 to 0.98 among cultivar pairs, and 72% of pair-wise comparisons exceeded 0.5. UPGMA (unweighted pair-group method with arithmetic averaging) clustering and principle component analysis revealed four main clusters, I–IV; most modern hybrid cultivars grouped in II, whereas most vintage cultivars grouped in I. Clusters III and IV contained three and two cultivars, respectively. Some groups of cultivars closely related by pedigree exhibited high bootstrap values, but lower values (<50%) were obtained for cluster II and its four subgroups. Unique fingerprints for all 74 cultivars were obtained by a minimum of seven AFLP primer pairs, despite inclusion of some closely related cultivars. This study demonstrated that AFLP markers are effective for obtaining unique fingerprints of, and assessing genetic diversity among, tomato cultivars.Key words: Lycopersicon esculentum, AFLPs, DNA fingerprinting, genetic diversity, phenetic relationships.


HortScience ◽  
2006 ◽  
Vol 41 (4) ◽  
pp. 968A-968 ◽  
Author(s):  
Jianjun Chen ◽  
Richard J. Henny ◽  
Pachanoor S. Devanand ◽  
Chih-Cheng T. Chao

Peace lily (Spathiphyllum Schott) is one of the most popular tropical ornamental foliage plants and is used worldwide for interiorscaping. However, little information is available on the genetic relationships of cultivars. Using amplified fragment length polymorphism (AFLP) markers with near-infrared fluorescence-labeled primers, this study analyzed genetic relatedness of 63 commercial cultivars and breeding lines. Forty-eight EcoRI + 2/MseI + 3 primer set combinations were initially screened, from which six primer sets were selected and used in this investigation. All cultivars were clearly differentiated by their AFLP fingerprints, and the relationships were analyzed using the unweighted pair-group method of arithmetic average cluster analysis (UPGMA). The 63 cultivars were divided into four clusters. All commercial cultivars or breeding lines resulted from crosses of some of the cultivars, a total of 45, were positioned in cluster I with Jaccard's similarity coefficients between 0.61 and 0.88. There was only one cultivar in cluster II. Cluster III contained 16 cultivars; they are either species or breeding lines generated from interspecific hybridization. Cluster IV had one unknown species. This study provides genetic evidence as to why cultivars from cluster I and III are not readily crossable because the Jaccard's similarity coefficient between the two clusters was only 0.35. Results also indicate that commercial cultivars are genetically close. Strategies for increasing genetic diversity of cultivated peace lily should be sought for future breeding efforts.


2004 ◽  
Vol 129 (1) ◽  
pp. 81-87 ◽  
Author(s):  
Jianjun Chen ◽  
Richard J. Henny ◽  
David J. Norman ◽  
Pachanoor S. Devanand ◽  
Chih-Cheng T. Chao

Dieffenbachia Schott is an important ornamental foliage plant genus. A total of 30 species has been recognized, but most cultivars come from or are related to a single species, D. maculata (Lodd.) G. Don. At least 11 of the cultivars are sports or somaclonal variants. As a result, the potential lack of genetic diversity in cultivated Dieffenbachia has become a concern. However, no research has been conducted to determine the genetic relatedness of the cultivars. This study analyzed the genetic similarity of 42 Dieffenbachia cultivars using amplified fragment length polymorphism (AFLP) markers. Six primer sets, selected from an initial screening of 48, generated a total of 453 scorable AFLP fragments of which 323 (71%) are polymorphic. All cultivars were clearly differentiated by their AFLP fingerprints. A dendrogram was constructed using the unweighted pair-group method of arithmetic averages, and principal coordinated analysis was carried out to show multiple dimensions of the distribution of the cultivars. The 42 cultivars were divided into three clusters; clusters I and II comprise 18 and 23 cultivars, respectively. Jaccard's similarity coefficients for cultivars in the clusters I and II varied from 0.44 to 0.95 and 0.41 to 0.87, respectively. These results indicate that broadening the genetic variability in the Dieffenbachia gene pool is needed, but the genetic similarity of many cultivars is not as close as previously thought. Additionally, Jaccard's similarity coefficients between most sports or somaclonal variants and their parents were 0.73 or lower, suggesting that accumulation of somatic mutations through tissue culture may play a role in the increased variation between some sports or variants and their parents.


2011 ◽  
Vol 46 (9) ◽  
pp. 1035-1044 ◽  
Author(s):  
Patrícia Coelho de Souza Leão ◽  
Sérgio Yoshimitsu Motoike

The objective of this work was to analyze the genetic diversity of 47 table grape accessions, from the grapevine germplasm bank of Embrapa Semiárido, using 20 RAPD and seven microsatellite markers. Genetic distances between pairs of accessions were obtained based on Jaccard's similarity index for RAPD data and on the arithmetic complement of the weighted index for microsatellite data. The groups were formed according to the Tocher's cluster analysis and to the unweighted pair‑group method with arithmetic mean (UPGMA). The microsatellite markers were more efficient than the RAPD ones in the identification of genetic relationships. Information on the genetic distance, based on molecular characteristics and coupled with the cultivar agronomic performance, allowed for the recommendation of parents for crossings, in order to obtain superior hybrids in segregating populations for the table grape breeding program of Embrapa Semiárido.


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