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dc.contributor.authorMignouna, H.D.en_US
dc.contributor.authorAbang, Mathew M.en_US
dc.contributor.authorAsiedu, Roberten_US
dc.date.accessioned2018-08-09T06:40:34Zen_US
dc.date.available2018-08-09T06:40:34Zen_US
dc.identifier.urihttps://hdl.handle.net/10568/96375en_US
dc.titleHarnessing modern biotechnology for tropical tuber crop improvement: yam (Dioscorea spp.) molecular breedingen_US
cg.authorship.typesCGIAR and advanced research instituteen_US
cg.subject.iitaYAMen_US
cg.subject.iitaPLANT BREEDINGen_US
dcterms.abstractYams (Dioscorea spp.) constitute a staple food crop for over 100 million people in the humid and subhumid tropics. They are polyploid and vegetatively propagated. The Guinea yams, Dioscorea rotundata and D. cayenensis, are the most important yams in West and Central Africa where they are indigenous, while D. alata (referred to as water yam) is the most widely distributed species globally. The genetics of yams is least understood among the major staple food crops due to several biological constraints and research neglect. Research to unravel the apparent complexity of the yam genome will have far-reaching implications for genetic improvement of this important tuber crop. Some progress has been made in recent years in germplasm characterization and the development of molecular markers for genome analysis. A genetic linkage map based on amplified fragment length polymorphism (AFLP) markers has been constructed for Guinea and water yams. These linkage maps were used to scan the genome for quantitative trait loci (QTL) associated with genes conferring resistance to Yam Mosaic Virus (YMV) in D. rotundata and anthracnose (Colletotrichum gloeosporioides) in D. alata. In addition, candidate random amplified polymorphic DNA (RAPD) markers associated with major genes controlling resistance to YMV and anthracnose have been identified that could be used for selection and pyramiding of YMV and anthracnose resistance genes in yam improvement. Also, molecular markers such as RAPDs, AFLPs, and microsatellites or simple sequence repeats (SSRs) have been developed for yam genome analysis. An initial c-DNA library has been constructed in order to develop expressed sequence tags (ESTs) for gene discovery and as a source of additional molecular markers. This paper will review the advances made, discuss the implications for yam genetic improvement and germplasm conservation, and outline the direction for future research.en_US
dcterms.accessRightsOpen Accessen_US
dcterms.available2003-12-31en_US
dcterms.bibliographicCitationMignouna, H.D., Abang, M.M. & Asiedu, R. (2003). Harnessing modern biotechnology for tropical tuber crop improvement: yam (Dioscorea spp.) molecular breeding. African Journal of Biotechnology, 2(12), 478-485.en_US
dcterms.extentp. 478-485en_US
dcterms.issued2003-12en_US
dcterms.languageenen_US
dcterms.publisherAcademic Journalsen_US
dcterms.subjectyamsen_US
dcterms.subjectdioscorea rotundataen_US
dcterms.subjectcrop improvementen_US
dcterms.subjectmodern biotechnologyen_US
dcterms.subjectmolecular breedingen_US
dcterms.typeJournal Articleen_US
cg.contributor.affiliationVirginia Polytechnic Institute and State Universityen_US
cg.contributor.affiliationInternational Center for Agricultural Research in the Dry Areasen_US
cg.contributor.affiliationInternational Institute of Tropical Agricultureen_US
cg.identifier.doihttps://doi.org/10.5897/AJB2003.000-1097en_US
cg.coverage.regionAfricaen_US
cg.coverage.regionWestern Africaen_US
cg.coverage.regionMiddle Africaen_US
cg.coverage.countryBeninen_US
cg.coverage.countryBurkina Fasoen_US
cg.coverage.countryCôte d'Ivoireen_US
cg.coverage.countryGhanaen_US
cg.coverage.countryNigeriaen_US
cg.coverage.countrySierra Leoneen_US
cg.coverage.countryTogoen_US
cg.coverage.iso3166-alpha2BJen_US
cg.coverage.iso3166-alpha2BFen_US
cg.coverage.iso3166-alpha2CIen_US
cg.coverage.iso3166-alpha2GHen_US
cg.coverage.iso3166-alpha2NGen_US
cg.coverage.iso3166-alpha2SLen_US
cg.coverage.iso3166-alpha2TGen_US
cg.contributor.donorGatsby Charitable Foundationen_US
cg.reviewStatusPeer Reviewen_US
cg.issn1684-5315en_US
cg.volume2en_US
cg.issue12en_US


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