AFLP analysis of genetic variation within the two economically important Anatolian grapevine (Vitis vinifera L.) varietal groups

Genome ◽  
2006 ◽  
Vol 49 (5) ◽  
pp. 467-475 ◽  
Author(s):  
Ali Ergül ◽  
Kemal Kazan ◽  
Sümer Aras ◽  
Volkan Çevik ◽  
Hasan Çelik ◽  
...  
Keyword(s):  
Vitis Vinifera ◽  
Group Method ◽  
Vitis Vinifera L ◽  
Aflp Analysis ◽  
Pair Group ◽  
Length Polymorphisms ◽  
Upgma Cluster Analysis ◽  
History Of ◽  
Historical Role ◽  
The Rich

The Anatolian region of modern-day Turkey is believed to have played an important role in the history of grapevine (Vitis vinifera L.) domestication and spread. Despite this, the rich grape germplasm of this region is virtually uncharacterized genetically. In this study, the amplified fragment length polymorphisms (AFLP)-based genetic relations of the grapevine accessions belonging to the 2 economically important Anatolian table grape varietal groups known as V. vinifera 'Misket' (Muscat) and V. vinifera 'Parmak' were studied. Thirteen AFLP primer combinations used in the analyses revealed a total of 1495 (35.5% polymorphic) and 1567 (34.6% polymorphic) DNA fragments for the 'Misket' and 'Parmak' varietal groups, respectively. The unweighted pair-group method with arthimetic averaging (UPGMA) cluster analysis and principal coordinate analysis (PCA) conducted on polymorphic AFLP markers showed that both varietal groups contain a number of synonymous (similar genotypes known by different names) as well as homony mous (genetically different genotypes known by the same name) accessions. Our results also showed that 6 of the Anatolian 'Misket' genotypes were genetically very similar to V. vinifera 'Muscat of Alexandria', implying that these genotypes might have played some role in the formation of this universally known grape cultivar. Finally, the close genetic similarities found here between 'Muscat of Alexandria' and V. vinifera 'Muscat of Hamburg' support the recent suggestion that 'Muscat of Hamburg' probably originated from 'Muscat of Alexandria' through spontaneous hybridizations. Overall, the results of this study have implications for not only preservation and use of the Anatolian grape germplasm, but also better understanding of the historical role that this region has played during the domestication of grapes.Key words: 'Misket', 'Parmak', AFLP, Vitis vinifera L.

Genetic analysis of a heritage variety collection

2018 ◽  
Vol 17 (03) ◽  
pp. 232-244 ◽  
Author(s):  
J. M. Preston ◽  
B. V. Ford-Lloyd ◽  
L. M. J. Smith ◽  
R. Sherman ◽  
N. Munro ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Group Method ◽  
Niche Markets ◽  
Principal Coordinates Analysis ◽  
Pair Group ◽  
Landrace Diversity ◽  
Principal Coordinates ◽  
Length Polymorphisms ◽  
Seed Saving ◽  
History Of

AbstractLandraces (including heritage varieties) are an important agrobiodiversity resource offering considerable value as a buffer against crop failures, as a crop for niche markets, and as a source of diversity for crop genetic improvement activities underpinning future food security. Home gardens are reservoirs of landrace diversity, but some of the accessions held in them are vulnerable or threatened with extinction. Those associated with seed saving networks have added security, for example, ca. 800 varieties are stored in the Heritage Seed Library (HSL) of Garden Organic, UK. In this study, Amplified Fragment Length Polymorphisms-based genetic analysis of accessions held in the HSL was used to (a) demonstrate the range of diversity in the collection, (b) characterize accessions to aid collection management and (c) promote broader use of the collection. In total, 171 accessions were included from six crops: Vicia faba L., Pisum sativum L., Daucus carota L., Cucumis sativus L., Lactuca sativa L. and Brassica oleracea L. var. acephala (DC.) Metzq. Average expected heterozygosity ranged from 0.18 to 0.28 in D. carota; 0.02–0.18 in P. sativum; 0.05–0.18 in L. sativa; 0.15–0.26 in B. oleracea var. acephala; 0.15–0.37 in C. sativus and 0.07–0.36 in V. faba. Genetic diversity and Fst values generally reflected the breeding system and cultivation history of the different crops. Comparisons of the diversity found in heritage varieties with that found in commercial varieties did not show a consistent pattern. Principal coordinates analysis and Unweighted Pair Group Method with Arithmetic Mean cluster analysis were used to identify four potential duplicate accession pairs.

AFLP-based assessment of genetic diversity among nine alfalfa germplasms using bulk DNA templates

Genome ◽  
2003 ◽  
Vol 46 (1) ◽  
pp. 51-58 ◽  
Author(s):  
A Segovia-Lerma ◽  
R G Cantrell ◽  
J M Conway ◽  
I M Ray
Keyword(s):  
Genetic Diversity ◽  
Medicago Sativa ◽  
High Throughput ◽  
Genetic Distances ◽  
Group Method ◽  
Aflp Analysis ◽  
Dna Templates ◽  
Arithmetic Average ◽  
Pair Group ◽  
Large Numbers

Improving commercial utilization of perennial Medicago collections requires developing approaches that can rapidly and accurately characterize genetic diversity among large numbers of populations. This study evaluated the potential of using amplified fragment length polymorphism (AFLP) DNA markers, in combination with DNA bulking over multiple genotypes, as a strategy for high-throughput characterization of genetic distances (D) among alfalfa (Medicago sativa L.) accessions. Bulked DNA templates from 30 genotypes within each of nine well-recognized germplasms (African, Chilean, Flemish, Indian, Ladak, Medicago sativa subsp. falcata, Medicago sativa subsp. varia, Peruvian, and Turkistan) were evaluated using 34 primer combinations. A total of 3754 fragments were identified, of which 1541 were polymorphic. The number of polymorphic fragments detected per primer combination ranged from 20 to 85. Pairwise D estimates among the nine germplasms ranged from 0.52 to 1.46 with M. sativa subsp. falcata being the most genetically dissimilar. Unweighted pair-group method arithmetic average (UPGMA) analysis of the marker data produced two main clusters, (i) M. sativa subsp. sativa and M. sativa subsp. varia, and (ii) M. sativa subsp. falcata. Cluster-analysis results and D estimates among the Chilean, Peruvian, Flemish, and M. sativa subsp. varia germplasms supported the hypothesis that Peruvian was more similar to original Spanish introductions into Central and South America than Chilean. Hierarchical arrangement of the nine germplasms was supported by their respective geographic, subspecific, and intersubspecific hybrid origins. Subsets of as few as seven highly informative primer pairs were identified that produced comparable D estimates and similar heirarchical arrangements compared with the complete dataset. The results indicate that use of primer-pair subsets for AFLP analysis of bulk DNA templates could serve as a high-throughput system for accurately characterizing genetic diversity among large numbers of alfalfa populations.Key words: Medicago sativa, DNA bulking, genetic distance.

scholarly journals Генетический полиморфизм редких и малораспространенных аборигенных донских генотипов L

2019 ◽  
pp. 191-197 ◽  
Author(s):  
Elena Ilnitskaya ◽  
Lyudmila Naumova ◽  
Valentina Ganich ◽  
Sergey Tokmakov ◽  
Marina Makarkina
Keyword(s):  
Vitis Vinifera ◽  
Genetic Similarity ◽  
Genetic Distances ◽  
The Other ◽  
Vitis Vinifera L ◽  
Separate Branch ◽  
History Of ◽  
The Difference ◽  
Dna Profiles ◽  
Basic Minimum

История виноградарства на Дону насчитывает несколько веков, местные сорта винограда многообразны и специфичны. Микросателлитные маркеры широко используются для генотипирования сортов и подвоев винограда, при изучении происхождения сортов и анализе их родословной. Целью исследования было изучение выборки редких и малораспространенных автохтонных донских сортов и сравнение их с другими аборигенными донскими генотипами на основе данных ДНК-анализа. В исследования включены 23 стародавних донских сорта. Генотипирование проводили методом микросателлитного профилирования. В исследовании использовали микросателлитные маркеры (SSR), рекомендованные в качестве основного минимального набора для ДНК-паспортизации сортов вида Vitis vinifera L.: VVMD5, VVMD7, VVMD27, VVS2, VrZAG62 и VrZAG79. По результатам проведенного анализа все изученные образцы показали сорт-специфическую комбинацию аллелей в идентифицированных ДНК-профилях. Количество выявленных аллелей составило в среднем 8 аллелей/локус. Наибольший полиморфизм в исследовании этой группы донских сортов был обнаружен в локусе VVMD5: идентифицировано 10 аллелей на локус, наименьшее - в локусе VrZAG62: 6 аллелей/локус. Основываясь на данных SSR-анализа, степень генетического сходства сортов оценивали с использованием метода UPGMA. Кластерный анализ матрицы генетических дистанций, созданный на основе выявленных значений аллелей в шести микросателлитных локусах исследуемых сортов, определил несколько групп генотипов. Сорт Красностоп золотовский выделился в отдельную ветвь, что указывает на различия между этим генотипом и другими сортами исследуемой выборки. Наивысший уровень генетического сходства наблюдался между следующими парами сортов: Крестовский и Бургундский, Шилохвостый и Мушкетный, Кумшацкий черный и Ефремовский.The history of viticulture on the Don goes back several centuries. Local grapevine varieties are diverse and peculiar. Microsatellite markers are widely used in genotyping grapevine cultivars and rootstocks, in grapevine origin and breeding background analysis. Our study aimed to examine samples of rare and less common autochthonous Don varieties, and compare them with the other aboriginal Don genotypes using DNA data. The study involved 23 traditional Don varieties. The genotyping was done by microsatellite profiling. The study used microsatellite (SSR) markers recommended as the basic minimum set for DNA-certification of the genotypes of Vitis vinifera L.: VVMD5, VVMD7, VVMD27, VVS2, VrZAG62 and VrZAG79. Based on the findings, all the studied samples demonstrated variety-specific combination of alleles in the identified DNA profiles. The number of detected alleles on average was 8 alleles/locus. The greatest polymorphism in the studied group of Don varieties was detected in VVMD5 locus: 10 alleles per locus were identified, the smallest in VrZAG62 locus: 6 alleles/locus. UPGMA method was used to assess the extent of genetic similarity of the varieties based on SSR-genotyping data. Based on determined allele values of the studied varieties, cluster analysis of the genetic distances matrix determined several groups of genotypes. ‘Krasnostop zolotovskiy’ variety stood out as a separate branch, which indicates the difference between this genotype and the other varieties of the studied sampling. The highest level of genetic similarity was observed between the following pairs of varieties: ‘Krestovskiy’ and ‘Burgundskiy’, ‘Shilohvostyi’ and ‘Mushketnyi’, ‘Kumshatskiy chornyi’ and ‘Efremovskiy’.

scholarly journals Genetic structure and differentiation in cultivated grape, Vitis vinifera L.

2003 ◽  
Vol 81 (3) ◽  
pp. 179-192 ◽  
Author(s):  
MALLIKARJUNA K. ARADHYA ◽  
GERALD S. DANGL ◽  
BERNARD H. PRINS ◽  
JEAN-MICHEL BOURSIQUOT ◽  
M. ANDREW WALKER ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Vitis Vinifera ◽  
Gene Diversity ◽  
Genetic Relationships ◽  
Vitis Vinifera L ◽  
Significant Heterogeneity ◽  
Multivariate Relationships ◽  
History Of ◽  
Single Complex ◽  
Grape Cultivars

222 cultivated (Vitis vinifera) and 22 wild (V. vinifera ssp. sylvestris) grape accessions were analysed for genetic diversity and differentiation at eight microsatellite loci. A total of 94 alleles were detected, with extensive polymorphism among the accessions. Multivariate relationships among accessions revealed 16 genetic groups structured into three clusters, supporting the classical eco-geographic grouping of grape cultivars: occidentalis, pontica and orientalis. French cultivars appeared to be distinct and showed close affinity to the wild progenitor, ssp. sylvestris from south-western France (Pyrenees) and Tunisia, probably reflecting the origin and domestication history of many of the old wine cultivars from France. There was appreciable level of differentiation between table and wine grape cultivars, and the Muscat types were somewhat distinct within the wine grapes. Contingency χ2 analysis indicated significant heterogeneity in allele frequencies among groups at all loci. The observed heterozygosities for different groups ranged from 0·625 to 0·9 with an overall average of 0·771. Genetic relationships among groups suggested hierarchical differentiation within cultivated grape. The gene diversity analysis indicated narrow divergence among groups and that most variation was found within groups (∼85%). Partitioning of diversity suggested that the remaining variation is somewhat structured hierarchically at different levels of differentiation. The overall organization of genetic diversity suggests that the germplasm of cultivated grape represents a single complex gene pool and that its structure is determined by strong artificial selection and a vegetative mode of reproduction.

scholarly journals SSR Markers Reveal the Genetic Diversity of Asian Cercis Taxa at the U.S. National Arboretum

HortScience ◽  
2017 ◽  
Vol 52 (4) ◽  
pp. 498-502 ◽  
Author(s):  
Chandra S. Thammina ◽  
David L. Kidwell-Slak ◽  
Stefan Lura ◽  
Margaret R. Pooler
Keyword(s):  
Genetic Diversity ◽  
Ssr Markers ◽  
The United States ◽  
Group Method ◽  
Cercis Canadensis ◽  
Landscape Plant ◽  
Pair Group ◽  
Upgma Cluster Analysis ◽  
Eastern Redbud ◽  
The U.S

The redbud (Cercis L. species) is a popular landscape plant grown widely in the United States. There are more than 20 cultivars of eastern redbud (Cercis canadensis L.) and at least three cultivars of Asian taxa (primarily Cercis chinensis Bunge) in the trade. The U.S. National Arboretum (USNA) has a diverse collection of Cercis germplasm collected in North America and Asia. Fourteen genomic simple sequence repeat (genomic-SSR) markers were used to analyze the genetic diversity of 53 accessions of Asian Cercis taxa from our collection, including C. chinensis, Cercis chingii Chun, Cercis gigantea ined., Cercis glabra Pamp., Cercis racemosa Oliv., and Cercis yunnanensis Hu and W. C. Cheng. SSR markers detected an average of 5.7 alleles per locus with a range of two to nine alleles. A dendrogram was generated by unweighted pair group method with arithmetic mean (UPGMA) cluster analysis using the Jaccard similarity coefficient. Four major clusters were identified. Accessions tended to group by taxa or provenance, but with some notable exceptions caused either by misidentification or nomenclatural confusion in the species. This information will be used for collection management and for making decisions in the breeding program to maximize genetic diversity of cultivated Cercis.

scholarly journals Assessment of Genetic Diversity in Cultivated Tomato (Solanum Lycopersicum L.) Genotypes Using Rapd Primers

2013 ◽  
Vol 21 (1) ◽  
pp. 83-89 ◽  
Author(s):  
Saida Sharifova ◽  
Sabina Mehdiyeva ◽  
Konstantinos Theodorikas ◽  
Konstantinos Roubos
Keyword(s):  
Genetic Diversity ◽  
Rapd Analysis ◽  
Diversity Index ◽  
Random Amplified Polymorphic Dna ◽  
Arithmetic Mean ◽  
Similarity Coefficient ◽  
Group Method ◽  
Solanum Lycopersicum L ◽  
Pair Group ◽  
Upgma Cluster Analysis

Abstract Random Amplified Polymorphic DNA (RAPD) analysis was carried out on 19 Azerbaijan tomato genotypes, both cultivars and local populations. A total of 26 amplified products were revealed by 6 primers. The genetic similarity among evaluated genotypes ranged from 0.188 to 1.000. The lowest similarity was observed between cultivars ‘Azerbaijan’ and ‘Shakar’ (0.188), while the highest between ‘Elnur’ and ‘Garatag’ (1.000). The Unweighted Pair Group Method with Arithmetic Mean (UPGMA) cluster analysis based on Jaccard’s similarity coefficient divided genotypes into four main groups. The first group was the largest and consisted of 12 genotypes, while the fourth group was the smallest consisted of 1 genotype only. The most polymorphic primer was OPB-18 that presented a genetic diversity index of 0.823, while the least informative was primer OPG-17 with an index of 0.349. The average genetic diversity calculated from RAPD data was 0.665.

Genetic diversity in bambara groundnut (Vigna subterranea (L.) Verdc) landraces revealed by AFLP markers

Genome ◽  
2002 ◽  
Vol 45 (6) ◽  
pp. 1175-1180 ◽  
Author(s):  
F J Massawe ◽  
M Dickinson ◽  
J A Roberts ◽  
S N Azam-Ali
Keyword(s):  
Genetic Diversity ◽  
Genetic Relationships ◽  
Geographic Origin ◽  
Bambara Groundnut ◽  
Aflp Markers ◽  
Group Method ◽  
Aflp Analysis ◽  
Vigna Subterranea ◽  
Marker Assisted Breeding ◽  
Pair Group

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.

scholarly journals Keragaman genetik klon-klon karet (Hevea brasiliensis Muell. Arg) yang resisten dan rentan terhadap Corynespora casiicola berdasarkan penanda RAPD dan AFLP Genetic variation of rubber ( Hevea brasiliensis Muell. Arg) clones resistance and susceptible to Corynespora cassiicola using RAPD and AFLP markers

2016 ◽  
Vol 70 (2) ◽  
Author(s):  
Nurita TORUAN-MATHIUS ◽  
Z LALU ◽  
. SOEDARSONO ◽  
Hajrial ASWIDINNOOR
Keyword(s):  
Hevea Brasiliensis ◽  
Genetic Similarity ◽  
Pcr Amplification ◽  
Aflp Markers ◽  
Group Method ◽  
Aflp Analysis ◽  
Pair Group ◽  
Young Leaves ◽  
Cluster A ◽  
Susceptible Group

SummaryCorynespora leaf fall disease (CFLD) caused by the fungus Corynespora casiicola is one of the most important diseases of Hevea brasiliensis.CFLD was reported to cause serious damage on rubber productivity, and the disease has became more apparent in the recent years. The objectives of this study were (i) to analyze genetic similarities among several rubber clones resistance and susceptible to CFLD based on RAPD and AFLP markers, (ii) to compare the effectiveness of RAPD and AFLP markers. DNA genomic was extracted from young leaves of RRIM600, GT1, PB260, RRIC100, BPM1 (belongs to resistance group), PPN2058, PPN2444, and PPN2447 (belongs to susceptible group). Data were analyzed with NTSYS-pc program version 2.10, and a dendogram was created by cluster analysis using the unweighted pair group method on the basis of arithmetic averages (UPGMA). The results show that marker index AFLP (3.57) is higher than RAPD (1.02), it means that AFLP is more effective compared to RAPD. The average of genetic similarity AFLP (0.63) lower than RAPD (0.67) it means that AFLP is more discriminative than RAPD. Dendogram based on AFLP and RAPD were the best with at 0.65 level of genetic similarity cluster divided into two cluster A and B. Cluster A with a sub group A1 consisted of RRIC100, PPN2058 and PPN244 are belongs to resistance group), and sub group A2 consisted of (RRIM600, GT1, BPM1 and PB 260 are belongs to susceptible group), while cluster B only PPN2447 is belong to susceptible group. AFLP analysis show that one AFLP band of 110 bp resulting from PCR amplification using E-ACA/M-CAG (E-ACA/M-CAG110) primer pairs present in resistance clones, but absent in the susceptible clones. Meanwhile, application of 50 random primers decamer in RAPD analysis did not showed the specific band for either one of the group. It is concluded that AFLP marker analysis using EACA/M-CAG primer pair have a potential to differentiate resistance and the susceptible rubber clones to Corynespora. For the confirmation of the results more resistance and susceptible clones are needed for further test. RingkasanPenyakit gugur daun Corynespora (PDGC) yang disebabkan oleh patogen Corynespora asiicola, merupakan salah satu penyakit penting pada tanaman karet (Hevea brasiliensis). PGDC menyebabkan penurunan yang cukup serius terhadap produktivitas tanaman karet. Tujuan penelitian ini adalah untuk (i) mengidentifikasi kesamaan genetik antar beberapa klon yang tergolong tahan dan rentan dengan marka RAPD dan AFLP, dan (ii) mempelajari efektivitas kedua marka tersebut. DNA genomik diekstraksi dari daun muda klon RRIM600, GT1, PB260, BPM1, RRIC100 (tergolong resisten), PPN2058, PPN2444, dan PPN2447 (tergolong rentan ). Data dianalisis dengan NTSYS-pc program versi 2.10. Dendogram dibuat dengan analisis pengelompokan menurut metode Unweighted Pair Group berbasis Arithmetic Avarages (UPGMA). Hasil yang diperoleh menunjukkan bahwa marka indeks AFLP (3,57) lebih tinggi daripada RAPD (1,02), sehingga AFLP lebih efektif dibandingkan dengan RAPD. Rata-rata perkiraan kesamaan genetik AFLP (0,63) sedikit lebih rendah dari RAPD (0,67) sehingga AFLP relatif lebih diskriminatif daripada RAPD. Dendogram berdasarkan integrasi AFLP dan RAPD adalah yang paling baik, dimana pada rata-rata perkiraan kesamaan genetik (0,65) terbentuk dua kelompok yaitu A dan B. Kelompok A terdiri atas sub sub kelompok A1 yang beranggotakan (RRIC100, PPN2058 dan PPN244 yang tergolong resisten), dan sub group A2 yang beranggotakan (RRIM600, GT1, BPM1 dan PB 260 yang tergolong rentan) Sedang kelompok B beranggotakan hanya PN2447 yang tergolong rentan. Analisis AFLP menghasilkan satu pita AFLP dengan menggunakan pasangan primer EACA/M-CG (E-ACA/M-CAG110 ) secara konsisten diperoleh dari klon karet yang resisten, namun tidak ditemukan pada klon yang rentan. Sementara itu, aplikasi 50 primer acak dekamer dalam analisis RAPD tidak menghasilkan pita spesifik untuk kedua kelompok yang diuji. Disimpulkan bahwa analisis AFLP menggunakan pasangan primer EACA/M-CAG berpotensi untuk membedakan klon karet yang resisten dan rentan terhadap Corynespora. Untuk mengkorfirmasi hasil yang diperoleh, perlu dilakukan pengujian terhadap klon-klon yang resisten dalam jumlah yang lebih banyak

scholarly journals Polymorphism and Genetic Relationships among Tea Genotypes from Turkey Revealed by Amplified Fragment Length Polymorphism Markers

2009 ◽  
Vol 134 (4) ◽  
pp. 428-434 ◽  
Author(s):  
Salih Kafkas ◽  
Sezai Ercişli ◽  
Yıldız Doğan ◽  
Yaşar Ertürk ◽  
Ayhan Haznedar ◽  
...  
Keyword(s):  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Polymorphic Information Content ◽  
Genetic Relationships ◽  
Amplified Fragment Length Polymorphism ◽  
Group Method ◽  
Aflp Analysis ◽  
Black Sea Region ◽  
Pair Group

Individuals in most countries around the world drink tea (Camellia sinensis). Tea drinking has attained ceremonial status in many places as a social and medicinal beverage. Although tea is of great importance in Turkey's economy, little is known about the pattern of genetic variation among the various tea genotypes grown in Turkey. A total of 32 tea genotypes found at the Ataturk Tea and Horticulture Research Institute in the eastern Black Sea region of Turkey were sampled. Fluorescent dye amplified fragment length polymorphism (AFLP) markers and capillary electrophoresis were applied for molecular characterization. The AFLP analysis with six primer combinations generated 835 fragments of which 567 were polymorphic, corresponding to 69.8% polymorphism. Resolving powers of the AFLP primers ranged from 62.6 to 81.9, yielding a total of 437.8; the polymorphic information content (PIC) ranged from 0.76 to 0.83, with an average of 0.79. Genetic similarity values ranged from 0.68 to 0.92, with an average of 0.76. The dendrogram derived by unweighted pair group method with arithmetic mean algorithm (UPGMA) and principal coordinate analysis (PCoA) revealed that all tea genotypes could be clearly divided into four distinct clusters. The results of this study will provide valuable information to the tea cultivar breeding program for the purpose of parental selection.

scholarly journals Identificação de parentais e híbridos entre Vitis vinifera e Vitis rotundifolia utilizando polimorfismo enzimático e marcador RAPD

Bragantia ◽  
1996 ◽  
Vol 55 (2) ◽  
pp. 221-230 ◽  
Author(s):  
Haiko Enok Sawazaki ◽  
Celso Valdevino Pommer ◽  
Ilene Ribeiro Da Silva Passos ◽  
Maurilo Monteiro Terra ◽  
Erasmo José Paioli Pires
Keyword(s):  
Vitis Vinifera ◽  
Random Amplified Polymorphic Dna ◽  
Group Method ◽  
Vitis Rotundifolia ◽  
Pair Group ◽  
Unweighted Pair Group Method

Identificaram-se parentais e híbridos entre Vitis vinifera (videiras comuns) e V. rotundifolia (muscadínias), utilizando-se o polimorfismo enzimático e marcador RAPD (Random Amplified Polymorphic DNA). Os sistemas GOT (glutamato-oxalo-acetato-transaminase), IDH (isocitrato desidrogenase) e PGI (fosfoglucose isomerase) diferenciaram a muscadínia, sendo observadas cinco aloenzimas para o GOT, duas para o LAP (leucina aminopeptidase) e quatro para o EST (esterase). Os sistemas PGI e IDH apresentaram-se como diméricos com o fenótipo de quatro aloenzimas em duas regiões e três em uma região respectivamente. O marcador RAPD apresentou polimorfismo que permitiu a diferenciação entre todos os cultivares. Os dendrogramas UPGMA (unweighted pair-group method with aritmetic mean) obtidos pelas isoenzimas e pelo marcador RAPD foram semelhantes, sendo a aproximação mais forte entre 'Itália' e 'Rubi' que se ligaram aos cultivares Patrícia e A Dona. Os cultivares Piratininga e Eugênio, também bastante próximos, foram os seguintes a se ligarem às demais viníferas. Pelo polimorfismo enzimático e marcador RAPD, a muscadínia ficou bastante isolada dos outros grupos. Pelo método RAPD, aplicado às muscadínias, ao híbrido da Carolina do Norte NC66 C203-9, a um possível híbrido e seu parental feminino, observou-se o seguinte: os híbridos foram intermediários às muscadínias e viníferas, porém o possível híbrido se assemelhou ao parental feminino, enquanto o NC66203-9 apresentou bandas provenientes das muscadínias e viníferas, comprovando sua origem híbrida.

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