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Genetic Diversity of Cherry Laurel (Laurocerasus officinalis Roemer) BY SSR Markers

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dc.contributor.author Islam, Ali
dc.contributor.author Orta, Hale
dc.contributor.author Aka Kacar, Yildiz
dc.contributor.author Donmez, Dicle
dc.date.accessioned 2024-03-18T11:01:46Z
dc.date.available 2024-03-18T11:01:46Z
dc.date.issued 2023
dc.identifier.citation Islam, A., Orta, H., Aka Kaçar, Y., Dönmez, D. (2023). Genetic Diversity of Cherry Laurel (Laurocerasus officinalis Roemer) BY SSR Markers. J. Agric. Sci.-Tarim Bilim. Derg., 29(1), 239-248. https://doi.org/10.15832/ankutbd.930258 en_US
dc.identifier.issn 1300-7580
dc.identifier.issn 2148-9297
dc.identifier.uri http://dx.doi.org/10.15832/ankutbd.930258
dc.identifier.uri https://www.webofscience.com/wos/woscc/full-record/WOS:000977218600021
dc.identifier.uri http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/4703
dc.description WoS Categories: Agriculture, Multidisciplinary en_US
dc.description Web of Science Index: Science Citation Index Expanded (SCI-EXPANDED) en_US
dc.description Research Areas: Agriculture en_US
dc.description.abstract Cherry laurel (Laurocerasus officinalis) belongs to the Rosacea family. The main distribution area for edible cherry laurels is the Blacksea shores in Turkey. In the study, it was aimed to reveal the differences among the various cherry laurel genotypes by using the SSR molecular marker technique. Cherry laurel genotypes were selected from the Black Sea Region of Turkey. A total of 15 SSR primer pairs were developed and used for Prunus species, and the phylogenetic relationship and polymorphism rates were also demonstrated. As a result, 13 SSR primers resulted in scorable DNA band profiles. UDAp-401 SSR primer was detected with a minimum of 3 alleles and BBCT001 primer with a maximum of 17 alleles. The average number of alleles was observed at 9 per locus. Whereas, the average number of polymorphic bands per SSR marker was calculated as 8.38. Additionally, 109 polymorphic DNA profiles were obtained from a total of 117, and the polymorphism rate was calculated as 93.5%. The band patterns resulting from SSR analysis showed multiple alleles, suggesting polyploidy in cherry laurel. In conclusion, we determined that the SSR molecular markers could be used to identify the different cherry laurel genotypes. Furthermore, these results depicted that among the different genotypes sampled there is significant genetic variability that can be useful for future research and breeding programs. en_US
dc.description.sponsorship TUBITAK [115O564] en_US
dc.language.iso eng en_US
dc.publisher GALENOS PUBL HOUSE-ISTANBUL en_US
dc.relation.isversionof 10.15832/ankutbd.930258 en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Prunus laurocerasus L, DNA, Polymorphism, primer en_US
dc.subject PERSICA L. BATSCH, SWEET CHERRY, PRUNUS-AVIUM, PEACH, DNA, LOCI en_US
dc.title Genetic Diversity of Cherry Laurel (Laurocerasus officinalis Roemer) BY SSR Markers en_US
dc.type article en_US
dc.relation.journal JOURNAL OF AGRICULTURAL SCIENCES-TARIM BILIMLERI DERGISI en_US
dc.contributor.department Ordu Üniversitesi en_US
dc.contributor.authorID 0000-0002-2165-7111 en_US
dc.contributor.authorID 0000-0001-5314-7952 en_US
dc.identifier.volume 29 en_US
dc.identifier.issue 1 en_US
dc.identifier.startpage 239 en_US
dc.identifier.endpage 248 en_US


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