Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/2912
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dc.contributor.authorWachira, Francis N.-
dc.contributor.authorPowell, Wayne-
dc.contributor.authorWaugh, Robbie-
dc.date.accessioned2017-01-13T06:59:40Z-
dc.date.available2017-01-13T06:59:40Z-
dc.date.issued1997-
dc.identifier.citationHeredity 78 (1997) 603–611en_US
dc.identifier.issn1365-2540-
dc.identifier.urihttp://web.a.ebscohost.com/ehost/pdfviewer/pdfviewer?sid=cdab1c99-1a4a-4f09-a910-5f7aa37d79c0%40sessionmgr4006&vid=0&hid=4106-
dc.identifier.urihttp://repository.seku.ac.ke/handle/123456789/2912-
dc.description.abstractMembers of the genus Camellia interbreed relatively freely and several natural species hybrids exist. Species introgression into the cultivated germplasm of tea, Camellia sinensis L. (O. Kuntz), from related Camellia species has been postulated, and it is thought that teas currently under cultivation are not archetypal varieties. Randomly amplified polymorphic DNAs (RAPDs) and organelle-specific polymerase chain reactions were used to establish the affinities among cultivated tea and its wild relatives. The measures of similarity obtained indicated that RAPDs were taxonomically informative in Camellia, and the species relationships revealed were generally consistent with those obtained using morphological, compatibility and terpenoid affinities. Species-specific RAPD products and products potentially diagnostic of introgressive hybridization into the cultivated gene pool were identified. The organellar genomes were remarkably conserved, with polymorphism detected in only one of four noncoding regions in the chloroplast and mitochondrial genomes.en_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.subjectCamellia spp.en_US
dc.subjectgene introgressionen_US
dc.subjectpheneticsen_US
dc.subjectrandomly amplified polymorphic DNAen_US
dc.subjectsimilarityen_US
dc.titleAn assessment of genetic diversity among Camellia sinensis L. (cultivated tea) and its wild relatives based on randomly amplified polymorphic DNA and organelle-specific STS.en_US
dc.typeArticleen_US
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