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Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa

Thesis (MSc)--Stellenbosch University, 2017.

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Main Author: Kwalimba, Lawrence
Other Authors: Roodt-Wilding, Rouvay
Format: Thesis
Language:en_ZA
Published: Stellenbosch : Stellenbosch University 2017
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access_status_str Open Access
author Kwalimba, Lawrence
author2 Roodt-Wilding, Rouvay
author_browse Kwalimba, Lawrence
Roodt-Wilding, Rouvay
author_facet Roodt-Wilding, Rouvay
Kwalimba, Lawrence
author_sort Kwalimba, Lawrence
collection Thesis
dc_rights_str_mv Stellenbosch University
description Thesis (MSc)--Stellenbosch University, 2017.
format Thesis
id oai:scholar.sun.ac.za:10019.1/102603
institution Stellenbosch University (South Africa)
language en_ZA
last_indexed 2026-06-10T12:45:40.057Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from SUNScholar — Stellenbosch University Repository
publishDate 2017
publishDateRange 2017
publishDateSort 2017
publisher Stellenbosch : Stellenbosch University
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spelling oai:scholar.sun.ac.za:10019.1/102603 Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa Kwalimba, Lawrence Roodt-Wilding, Rouvay Tobutt, Kenneth Richard Pieterse, Werner-Marcel Horstmann, Carl Stellenbosch University. Faculty of AgriSciences. Dept. of Genetics. Peaches -- Western Cape -- South Africa Prunus persica -- Molecular fingerprinting Prunus persica -- Molecular characterization UCTD Thesis (MSc)--Stellenbosch University, 2017. ENGLISH ABSTRACT: Peaches and nectarines are important deciduous fruits in South Africa, both belonging to the species Prunus persica. The Agricultural Research Council (ARC) at Infruitec-Nietvoorbij in the Western Cape is the primary source of peach cultivars in South Africa. The germplasm from which these cultivars are developed is maintained at Bien Donne Research Farm (Paarl, Western Cape) and includes the reference collection for the Department of Agriculture, Forestry and Fisheries (DAFF). The germplasm collection has only been phenotyped morphologically and could be prone to errors and duplications. This study had two aims; firstly it aimed to utilize molecular marker technology (i.e. microsatellites markers) to fingerprint the germplasm collection to facilitate authentication. Secondly, the study aimed at employing functional markers for two agronomic traits of economic interest i.e. the peach/nectarine trait (hairy fruit epidermis) and white/yellow flesh colour. Nine reported polymorphic microsatellite markers were selected for the fingerprinting of 206 peach accessions, 20 almond accessions and seven hybrid accessions. One marker amplified multiple loci in both peaches and almonds while another marker did not amplify in either the almonds or the hybrids, and these were excluded. Therefore, the ARC peach accessions were successfully fingerprinted with eight microsatellite markers, and the almonds and hybrids with seven. Clustering analysis found fifty-eight accessions, including eighteen accession from the reference collection, were either misidentified or unresolved needing further molecular and morphological analysis. The accessions belonging to the reference collection are maintained by DAFF and were considered authentic prior to this study. The germplasm was characterized for the peach/nectarine trait (hairy fruit epidermis) as controlled by the MYB25 gene. It has been reported that a retrotransposon insertion in the third exon of the MYB25 gene disrupts formation of epidermal hairs in nectarine. The marker indelG was developed and fluorescently labelled and used to detect the presence of the retrotransposon insertion (g allele) or its absence (G allele). Peaches were observed to have at least one G allele while nectarines were homozygous for the g allele. Seventy-five accessions were genotyped as homozygous gg (nectarine), 35 accessions were heterozygous G/g (peach) and 96 were homozygous GG (peach). The heterozygous peaches can be intercrossed to develop new nectarine cultivars from peaches. The G allele, indicative of hairy fruit epidermis, was found in the almonds and some hybrids. Follow up studies for the role of the MYB25 gene in other Prunus species, especially in apricot (hairy), plum (glabrous) and cherry (glabrous), are recommended. The primers used in this study can be multiplexed with other primers and used for characterizing large number of samples at a relatively lower cost. The germplasm collection was also genotyped for the CCD4 gene that control the expression of white or yellow flesh colour. White flesh is the wildtype while yellow flesh results from loss of gene function through any of three mutations: a frameshift mutation at the TC microsatellite region, an A to T substitution (SNP) or a retrotransposon insertion. Three novel primer sets including fluorescently labelled primer pairs were designed to detect these mutations. The primer pair amplifying the TC microsatellite region (CCD4-SSR) in the CCD4 gene identified the wild type allele, a frameshift mutant and a very rare reversion allele in the accessions Overall, 25 accessions had the 122/122 bp genotype associated with white flesh, 138 accessions had the 124/124 bp genotype associated with yellow flesh colour, 42 accessions had the 122/124 bp genotype associated with the white flesh and one accession had the 124/128 bp genotype containing a reversion mutation associated with white flesh. The primer set amplifying the presence of the SNP (CCD-SNP) and its absence (CCD4-NoSNP) detected this SNP in 26 accessions, two of which were shown to be homozygous for the SNP mutation. The primer sets detecting the presence or absence of the retrotransposon (CCD4-Retro and CCD4-NoRetro) were not informative and the accessions could not be genotyped for this mutation. Therefore, the characterization of the flesh colour was incomplete and the deduced flesh colour are mostly tentative: with 33 accessions deduced as white flesh, 172 accessions as yellow flesh and 18 accessions as inconsistent and needing further follow up. Nevertheless, the partial genotypes and deduced phenotypes are useful and informative when designing of crosses in regard to flesh colour. The primers detecting the retrotransposon should be redesigned and used to complete flesh colour genotyping. Overall, the microsatellite fingerprinting gave baseline data useful for future repropagation while molecular characterization for peach/nectarine and flesh colour will aid in the design of crosses with predictable outcomes. This study, therefore, lays a solid foundation for future molecular characterization and utilization in the ARC peach breeding programme. AFRIKAANSE OPSOMMING: Geen opsomming beskikbaar Masters 2017-11-21T14:10:02Z 2017-12-11T10:30:43Z 2018-05-22T03:00:05Z 2017-12 Thesis http://hdl.handle.net/10019.1/102603 en_ZA Stellenbosch University 128 pages application/pdf application/pdf Stellenbosch : Stellenbosch University
spellingShingle Peaches -- Western Cape -- South Africa
Prunus persica -- Molecular fingerprinting
Prunus persica -- Molecular characterization
UCTD
Kwalimba, Lawrence
Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title_full Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title_fullStr Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title_full_unstemmed Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title_short Molecular fingerprinting and molecular characterization of the ARC's peach collection in South Africa
title_sort molecular fingerprinting and molecular characterization of the arc s peach collection in south africa
topic Peaches -- Western Cape -- South Africa
Prunus persica -- Molecular fingerprinting
Prunus persica -- Molecular characterization
UCTD
url http://hdl.handle.net/10019.1/102603
work_keys_str_mv AT kwalimbalawrence molecularfingerprintingandmolecularcharacterizationofthearcspeachcollectioninsouthafrica