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   <subfield code="a">Genetic diversity, structure and fruit trait associations in Greek sweet cherry cultivars using microsatellite based (SSR/ISSR) and morpho-physiological markers</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ioannis Ganopoulos, Konstantinos Kazantzis, Ioannis Chatzicharisis, Irene Karayiannis, Athanasios Tsaftaris]</subfield>
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   <subfield code="a">It is important to couple phenotypic analysis with genetic diversity for germplasm conservation in gene bank collections. The use of molecular markers supports the study of genetic marker-trait associations of biological and agronomic interest on diverse genetic material. In this report, 19 Greek traditional sweet cherry cultivars and two international cultivars, which were used as controls, were grown in Greece and characterized for 17 morpho-physiological traits, 15 simple sequence repeat (SSR) loci and 10 inter simple sequence repeat (ISSR) markers. To our knowledge, this is the first report on molecular genetic diversity studies in sweet cherry in Greece. Principal component analysis (PCA) of nine qualitative and eight quantitative morphological parameters explain over 77.33% of total variability in the first five axes. The SSR markers yielded a combined matching probability ratio (MPR) of 9.569×e−12. The 15 SSR loci produced a total of 92 alleles. Ten ISSR primers generated 91 bands, with an average of 9.1 bands per primer. Expected heterozygosity (gene diversity) values of 15 SSR loci and 10 ISSR markers averaged at 0.683 and 0.369, respectively. Based on stepwise multiple regression analysis (MRA), SSR alleles were found associated with harvest time and fruit polar diameter. Furthermore, three ISSR markers were correlated with fruit harvest and soluble solids and four ISSR markers were correlated with fruit skin color. Stepwise MRA identified six SSR alleles associated with harvest time with a high correlation (P&lt;0.001), with linear associations with high F values. Hence, data analyzed by the use of MRA could be useful in marker-assisted breeding programs when no other genetic information is available.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2011</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Sweet cherry</subfield>
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   <subfield code="a">MRA</subfield>
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   <subfield code="a">Fruit association markers</subfield>
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   <subfield code="a">Morpho-physiological traits</subfield>
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   <subfield code="a">SSR : Simple sequence repeat</subfield>
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   <subfield code="a">AFLP : Amplified fragment length polymorphism</subfield>
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   <subfield code="a">RAPD : Random amplified polymorphic DNA</subfield>
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   <subfield code="a">MRA : Multiple regression analysis</subfield>
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   <subfield code="a">PCA : Principal component analysis</subfield>
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   <subfield code="a">PCR : Polymerase chain reaction</subfield>
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   <subfield code="a">Ganopoulos</subfield>
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