Publication:
Individual identification and assessment of genetic diversity using microsatellite markers in racing pigeons raised in Turkiye

dc.contributor.authorŞentürk, Nursen
dc.contributor.authorTaşkın, Sebahat Dilara
dc.contributor.authorÇobanoğlu, Özden
dc.contributor.authorArdıclı, Sena
dc.contributor.buuauthorŞentürk, Nursen
dc.contributor.buuauthorTaşkın, Sebahat Dilara
dc.contributor.buuauthorÇOBANOĞLU, ÖZDEN
dc.contributor.buuauthorARDIÇLI, SENA
dc.date.accessioned2024-12-19T06:19:18Z
dc.date.available2024-12-19T06:19:18Z
dc.date.issued2024-06-05
dc.descriptionBu çalışma, 2023 tarihinde düzenlenen 13. International Hippocrates Congress on Medical and Health Sciences Kongresi‘nde bildiri olarak sunulmuştur.
dc.description.abstractThe implementation of a swift and economical molecular genetic approach, ensuring both efficacy and cost-effectiveness and facilitating population certification, is of utmost significance for breeders and the conservation of Turkiye's native pigeon biodiversity. In this study, we aimed to examine the genetic structure of racing pigeons (Columba livia domestica) raised in Turkiye using a genetic marker panel consisting of eight short tandem repeat (STR) loci. For this purpose, DNA was isolated from the shed feathers of 216 pigeons. Genomic DNA was amplified using the multiplex allele-specific PCR and subsequent capillary electrophoresis with ABI PRISM 3130XL Genetic Analyzer. Next, PCR products were analyzed in the GeneMapper Software program (Applied Biosystems). For parent testing, paternity index (PI), combined paternity index (CPI), and cumulative probability of paternity (CPP) were calculated. Furthermore, population genetic diversity was evaluated using heterozygosity (He), polymorphism information content (PIC), and Hardy–Weinberg equilibrium (HWE) testing. Results revealed that the total number of alleles is 81 and the number of alleles per locus varies between 4 and 19. The similarity rate between parent and offspring was calculated as 99.99% and above. Since no pedigree information was given when the samples were analyzed, obtaining this similarity ratio demonstrates the reliability of the panel. He values range from 0.362 to 0.919, and the PIC values range from 0.295 to 0.909. Loci PG-1, PG-2, and PG-3 show significant genetic diversity, with moderate to high PIC values reflecting varied allele frequencies in the population. Consequently, the set of seven STR markers (+ one sex marker) can be applied to identify and confirm parentage on a regular basis, thereby facilitating efficient breeding programs and ensuring genetic diversity conservation. This panel enables efficient pedigree analysis and gender determination, optimizing cost-effectiveness. The methodology presented in this study is ideal for pedigree analysis and breed certification in the Turkish pigeon breeding industry. Consequently, we affirm that the study data carries considerable national importance.
dc.identifier.doi10.30782/jrvm.1468165
dc.identifier.endpage84
dc.identifier.issue1
dc.identifier.startpage76
dc.identifier.urihttps://dergipark.org.tr/en/pub/jrvm/issue/86925/1468165
dc.identifier.urihttps://doi.org/10.30782/jrvm.1468165
dc.identifier.urihttps://dergipark.org.tr/en/download/article-file/3861500
dc.identifier.urihttps://hdl.handle.net/11452/49034
dc.identifier.volume43
dc.language.isoen
dc.publisherBursa Uludağ Üniversitesi
dc.relation.journalVeteriner Hekimlikte Araştırma Dergisi / Journal of Research in Veterinary Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectParentage testing
dc.subjectMicrosatellite markers
dc.subjectGenetic diversity
dc.subjectPopulation structure
dc.subjectColumba livia domestica
dc.titleIndividual identification and assessment of genetic diversity using microsatellite markers in racing pigeons raised in Turkiye
dc.title.alternativeYok
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationda041693-422d-424d-8ddf-35fb43e6e88b
relation.isAuthorOfPublicationb3ea478d-b033-4a23-84eb-d427d69d594c
relation.isAuthorOfPublication.latestForDiscoveryda041693-422d-424d-8ddf-35fb43e6e88b

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