Literature DB >> 15004289

ISSR-based clustering of cultivated flax germplasm is statistically correlated to thousand seed mass.

D Wiesnerová1, I Wiesner.   

Abstract

Inter-simple sequence repeat (ISSR)-polymerase chain reaction (PCR) polymorphism was generated to provide useful markers for assessment of genetic diversity within flax germplasm collections. We used nine previously selected anchored ISSR primers for fingerprinting of 53 flax cultivars or genotypes and obtained 62 scorable bands, from which 45 bands (72.6%) were polymorphic. An efficient separation of 53 flax accessions into four groups and eight subgroups was achieved using unweighted pair group method with arithmetic means (UPGMA) clustering procedure based on genetic similarity expressed by the Jaccard similarity coefficient (JSC). Clustering procedure within both groups and subgroups successfully produced smaller homogenous clusters, whereas clustering between the main four groups of flax accessions displayed only a continuous decrease of similarity with a weak clustering effect. Statistical significance of grouping and subgrouping within a cluster dendrogram was estimated by calculation of the error flag and cophenetic correlation parameter for each branch. Principal coordinates (PCO) analysis mostly confirmed the separation by UPGMA clustering. We observed a statistically significant correlation between the number of total vs polymorphic bands in ISSR patterns. A one-way analysis of variance (ANOVA) test confirmed statistically significant differences in the average thousand seed mass (TSM) between eight subclusters of flax accessions from an ISSR-PCR-based UPGMA dendrogram, which indicate statistical correlation between flax ISSR polymorphism (the structure of ISSR-based clustering) TSM.

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Year:  2004        PMID: 15004289     DOI: 10.1385/MB:26:3:207

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.860


  12 in total

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2.  Application of inter simple sequence repeat (ISSR) markers to plant genetics.

Authors:  I D Godwin; E A Aitken; L W Smith
Journal:  Electrophoresis       Date:  1997-08       Impact factor: 3.535

3.  PLANTING DENSITY INFLUENCES THE EXPRESSION OF GENETIC VARIATION IN SEED MASS IN WILD RADISH (RAPHANUS SATIVUS L.: BRASSICACEAE).

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6.  DNA typing of grapevines: a universal methodology and database for describing cultivars and evaluating genetic relatedness.

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7.  Fruit plant germplasm characterisation using molecular markers generated in RAPD and ISSR-PCR.

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Journal:  Cell Mol Biol Lett       Date:  2002       Impact factor: 5.787

8.  PCR-amplified microsatellites as markers in plant genetics.

Authors:  M Morgante; A M Olivieri
Journal:  Plant J       Date:  1993-01       Impact factor: 6.417

Review 9.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

10.  Genomic fingerprinting by microsatellite-primed PCR: a critical evaluation.

Authors:  K Weising; R G Atkinson; R C Gardner
Journal:  PCR Methods Appl       Date:  1995-04
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5.  Genome-Wide Association Study and Selection Signatures Detect Genomic Regions Associated with Seed Yield and Oil Quality in Flax.

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