Publication:
Development of SSR markers from Musa balbisiana for genetic diversity analysis among Thai bananas

dc.contributor.authorTiwa Rotchanapreedaen_US
dc.contributor.authorSirapope Wongniamen_US
dc.contributor.authorSasivimon C. Swangpolen_US
dc.contributor.authorPiyarat P. Chareonsapen_US
dc.contributor.authorNarongsak Sukkaewmaneeen_US
dc.contributor.authorJamorn Somanaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherPlant Genetic Conservation Project under the Royal Initiative of Her Royal Highness Princess Maha Chakri Sirindhornen_US
dc.contributor.otherRajabhat Universityen_US
dc.date.accessioned2018-12-11T01:57:03Z
dc.date.accessioned2019-03-14T08:04:16Z
dc.date.available2018-12-11T01:57:03Z
dc.date.available2019-03-14T08:04:16Z
dc.date.issued2016-08-01en_US
dc.description.abstract© 2016, Springer-Verlag Wien. Bananas in Thailand have been surveyed by our team to be at least 140 cultivars in the plantations, 10 wild species and, 4 introduced species. To characterize the genetic relationship of species and cultivars, a set of novel SSR markers was developed. Totaling 53 clones containing SSR motifs were isolated from SSR-enriched library of wild Musa balbisiana Colla ‘Tani’ (BB). Selected positive clones were used to design 28 primer pairs for amplification of 12 wild and 82 cultivar accessions with genome designations AA, AB, AAA, AAB, ABB, and BBB. These SSR markers loci were homology searched to the banana genomes to map their locations. The seven-sets multiplex PCR approach using four fluorescent-labeled universal primers were utilized for cost effectiveness. Capillary fragment analysis yielded the accurate size of amplicons for evaluation of particular patterns for each cultivar. Phylogram and Structure analysis presented the specific genotype of genome groups (A and B genotypes, polyploid hybrid genomes) and cultivar groups. By A:B specific alleles ratio, accurate genome designations of hybrids can be determined. Additionally, a marker, characterized to be partial plastid ycf2 gene, indicated the maternal identification of hybrid cultivars. One SSR marker was also preliminary tested with some wild species and advised to be the candidate fingerprinting marker for species identification. In conclusion, SSR marker sets developed here proved their exploitation in detailed identity and relationship of cultivated bananas, which would be useful for genetic conservation and ongoing breeding programs in Thailand and other areas.en_US
dc.identifier.citationPlant Systematics and Evolution. Vol.302, No.7 (2016), 739-761en_US
dc.identifier.doi10.1007/s00606-015-1274-2en_US
dc.identifier.issn16156110en_US
dc.identifier.issn03782697en_US
dc.identifier.other2-s2.0-84964330565en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43188
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84964330565&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleDevelopment of SSR markers from Musa balbisiana for genetic diversity analysis among Thai bananasen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84964330565&origin=inwarden_US

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