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8th INTERNATIONAL WHEAT CONFERENCE

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were clear differentiated. For RAPD-PCR analyses have been used 17 effective primers<br />

and assessed the intra-specie and inter-specie genetic diversity of the Triticum aestivum.<br />

According phenotypical traits as grain color, ear color, and awn, ear and steam, fragility,<br />

the intra-species diversity have been observed. The main fragment separation zone where<br />

within 2000-200 b.p. In whole, the 273 amplified fragments from 12 to 23 (16, in average)<br />

to one RAPD primer. Among 273 PCR fragments 54% were polymorphic between<br />

investigated genotypes, 46% have the similar length among all investigated samples. All<br />

primers in the different correlations established the monomorphic and polymorphic fragments<br />

between investigated samples. The monomorphic fragments can be considered<br />

as RAPD-markers for specie representatives. The genetic distances between investigated<br />

samples the more the less common amplified products. Revealed monomorphic bands of<br />

different varieties speculate similarity of the structural-functional organization of their<br />

genome. Each variety have own specific spectrum of the RAPD products, differed from<br />

each other by fragment quantity, their size and manifestation rate. Some primers revealed<br />

specific to their variety amplicons, however, it would be specific varietal characteristics.<br />

Significant differences on RAPD fragments quantities have been marked. The investigated<br />

samples have been differed in the numbers of the unique amplicons characterized<br />

for each variety. Based on the cluster analyses the dendrogram of the genetic similarity<br />

between investigated wheat samples has been constructed. The dendrogram have been<br />

revealed the high level of the intra-specific polymorphism.<br />

Therefore, molecular-genetic analyses give the possibility to reveal the specific genome<br />

markers, which can be used for varietal genome identifications. It shown, that the method<br />

of molecular marking based on RAPD-PCR allowed to identify the representatives of the<br />

Triticum aestivum species and to create phylogenetic links between different varieties.<br />

Unequivocal use of the varietal specific primers allowed to reducing expenditure and<br />

inputs which are necessary for collection analyses.<br />

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