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Comparison of AFLPs, RAPD markers, and isozymes for diversity assessment of garlic and detection of putative duplicates in germplasm collections

dc.contributor.authorIpek, M.
dc.contributor.authorIpek, A.
dc.contributor.authorSimon, P.W.
dc.contributor.buuauthorİPEK, AHMET
dc.contributor.department Ziraat Fakültesi
dc.contributor.departmentBahçe Bitkileri Ana Bilim Dalı
dc.contributor.scopusid6603912487
dc.date.accessioned2025-05-13T14:24:58Z
dc.date.issued2003-01-01
dc.description.abstractGarlic (Allium sativum L.) is an asexually propagated crop that displays much morphological diversity. Studies which have assessed garlic diversity with isozymes and randomly amplified polymorphic DNA (RAPD) markers generally agreed with the morphological observations but sometimes failed to discriminate clones. To discriminate among closely related garlic clones in more detail, we introduced amplified fragment-length polymorphism (AFLPs) to evaluate the genetic diversity and phenetic relatedness of 45 garlic clones and three A. longicuspis clones and we compared AFLP results with RAPD markers and isozymes. Three AFLP primer combinations generated a total of 183 polymorphic fragments. Although similarities between the clusters were low (≥0.30), some clones within the clusters were very similar (>0.95) with AFLP analysis. Sixteen clones represented only six different banding patterns, within which they shared 100% polymorphic AFLPs and RAPD markers, and likely are duplicates. In agreement with the results of other investigators, A. longicuspis and A. sativum clones were clustered together with no clear separation, suggesting these species are not genetically or specifically distinct. The topology of AFLP, RAPD, and isozyme dendrograms were similar, but RAPD and isozyme dendrograms reflected less and much less polymorphism, respectively. Comparison of unweighted pair group method with arithmetic averaging (UPGMA) dendrograms of AFLP, RAPD, and isozyme cluster analyses using the Mantel test indicated a correlation of 0.96, 0.55, and 0.57 between AFLP and RAPD, AFLP and isozyme, and RAPD and isozyme, respectively. Polymorphic AFLPs are abundant in garlic and demonstrated genetic diversity among closely related clones which could not be differentiated with RAPD markers and isozymes. Therefore, AFLP is an additional tool for fingerprinting and detailed assessment of genetic relationships in garlic.
dc.identifier.doi10.21273/jashs.128.2.0246
dc.identifier.endpage 252
dc.identifier.issn0003-1062
dc.identifier.issue2
dc.identifier.scopus2-s2.0-0037364143
dc.identifier.startpage246
dc.identifier.urihttps://hdl.handle.net/11452/52919
dc.identifier.volume128
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherAmerican Society for Horticultural Science
dc.relation.journalJournal of the American Society for Horticultural Science
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectMolecular marker comparisons
dc.subjectGenetic diversity
dc.subjectDuplicate accessions
dc.subjectAmplified fragment length polymorphism
dc.subjectAllium sativum
dc.subject.scopusGenetic Diversity and Yield Optimization in Garlic
dc.titleComparison of AFLPs, RAPD markers, and isozymes for diversity assessment of garlic and detection of putative duplicates in germplasm collections
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentZiraat Fakültesi/ Bahçe Bitkileri Ana Bilim Dalı
local.indexed.atScopus
relation.isAuthorOfPublication0fc2bd18-96db-49c3-ae1d-2fee8f4e3da4
relation.isAuthorOfPublication.latestForDiscovery0fc2bd18-96db-49c3-ae1d-2fee8f4e3da4

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