PCRRFLP of the ribosomal DNA internal transcribed spacers (ITS) provides markers for the A and B genomes in Musa L.

cg.authorship.typesCGIAR and developing country instituteen
cg.contributor.affiliationInternational Institute of Tropical Agricultureen
cg.contributor.affiliationUniversity of Port Harcourten
cg.contributor.affiliationMedical Research Council, Gambiaen
cg.contributor.donorMinistry of Foreign Affairs, the Netherlandsen
cg.coverage.countryNigeria
cg.coverage.iso3166-alpha2NG
cg.coverage.regionAfrica
cg.coverage.regionWestern Africa
cg.identifier.doihttps://doi.org/10.1007/s00122-003-1402-1en
cg.isijournalISI Journalen
cg.issn0040-5752en
cg.issn1432-2242en
cg.issue1en
cg.journalTheoretical and Applied Geneticsen
cg.reviewStatusPeer Reviewen
cg.subject.iitaPLANTAINen
cg.subject.iitaBANANAen
cg.volume108en
dc.contributor.authorNwakanma, D.C.en
dc.contributor.authorPillay, M.en
dc.contributor.authorOkoli, B.E.en
dc.contributor.authorTenkouano, A.en
dc.date.accessioned2018-08-09T06:40:36Zen
dc.date.available2018-08-09T06:40:36Zen
dc.identifier.urihttps://hdl.handle.net/10568/96393
dc.titlePCRRFLP of the ribosomal DNA internal transcribed spacers (ITS) provides markers for the A and B genomes in Musa L.en
dcterms.abstractMusa acuminata Colla (AA genomes) and Musa balbisiana Colla (BB genomes) are the diploid ancestors of modern bananas that are mostly diploid or triploid cultivars with various combinations of the A and B genomes, including AA, AAA, BB, AAB and ABB. The objective of this study was to identify molecular markers that will facilitate discrimination of the A and B genomes, based on restriction-site variations in the internal transcribed spacers (ITS) of the nuclear ribosomal RNA genes. The ITS regions of seven M. acuminata and five M. balbisiana accessions were each amplified by PCR using specific primers. All accessions produced a 700-bp fragment that is equivalent in size to the ITS of most plants. This fragment was then digested with ten restriction enzymes (AluI, CfoI, DdeI, HaeIII, HinfI, HpaII, MspI, RsaI, Sau3AI and TaqI) and fractionated in 2% agarose gels, stained with ethidium bromide and visualized under UV light. The RsaI digest revealed a single 530-bp fragment unique to the A genome and two fragments of 350-bp and 180-bp that were specific to the B genome. A further 56 accessions representing AA, AAA, AAB, AB and ABB cultivars, and synthetic hybrids, were amplified and screened with RsaI. All accessions with an exclusively A genome showed only the 530-bp fragment, while accessions having only the B-genome lacked the 530-bp fragment but had the 350-bp and 180-bp fragments. Interspecific cultivars possessed all three fragments. The staining intensity of the B-genome markers increased with the number of B-genome complements. These markers can be used to determine the genome constitution of Musa accessions and hybrids at the nursery stage, and, therefore, greatly facilitate genome classification in Musa breeding.en
dcterms.accessRightsLimited Access
dcterms.available2003-09-04
dcterms.bibliographicCitationNwakanma, D.C., Pillay, M., Okoli, B.E. & Tenkouano, A. (2003). PCR-RFLP of the ribosomal DNA internal transcribed spacers (ITS) provides markers for the A and B genomes in Musa L. Theoretical and Applied Genetics, 108(1), 154-159.en
dcterms.extentp. 154-159en
dcterms.issued2003-12
dcterms.languageen
dcterms.licenseCopyrighted; all rights reserved
dcterms.publisherSpringeren
dcterms.subjectmusaen
dcterms.subjectgenomesen
dcterms.typeJournal Article

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