Simple Sequence Repeat (SSR) Markers Differentiate Turkish Sour Cherry Germplasm

Authors

  • Yildiz A. Kacar Author
  • M. Selim Cetiner Author
  • Claudio Cantini Author
  • A.F. Iezzoni Author

DOI:

https://doi.org/10.71318/apom.2006.60.3.136

Abstract

Eighty-one tetraploid cherry selections, including sour cherry ( Prunus cerasusL.) and its progenitor species P. fruticosaPall., were compared using simple sequence repeat (SSR) marker analysis to determine the relationship of germplasm collected from Turkey to those collected from Russia and northern and eastern regions of Europe. SSR fragments were produced with all five primer pair – cherry selection combinations. Cherry selections exhibited high levels of polymorphism with 5 to 20 different putative alleles amplified per primer pair. The primer pair PMS 49, isolated from sweet cherry, showed a high level of polymorphism with 20 putative alleles identified. However, SSR analysis was not able to differentiate among some selections.

Overall, Turkish selections tended to group together and separated from other cherry selections. The Turkish germplasm did not exhibit many of the putative SSR alleles identified in the broader germplasm pool; however, it exhibited many novel alleles. This study demonstrated the importance of including germplasm from Turkey, an important ancestral region for sour cherry, when building a germplasm collection. It also demonstrated the utility of SSR markers in identifying genetic variation “gaps” within a germplasm collection.

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Published

2006-07-01

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How to Cite

Simple Sequence Repeat (SSR) Markers Differentiate Turkish Sour Cherry Germplasm. (2006). Journal of the American Pomological Society, 60(3), 136-143. https://doi.org/10.71318/apom.2006.60.3.136