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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

¹Genetic analysis of red pigmentation in ‘bon rouge’ pears (Pyrus communis L.)

Booi, Sonwabo January 2014 (has links)
>Magister Scientiae - MSc / European pear (Pyrus communis L.) is the third most important fruit in South Africa after citrus and apple. The Agricultural Research Council (ARC) breeding programme seeks to obtain a fully red coloured pear. Sports (mutants) with red skin and reddish leaves of various cultivars occur and some have been used in breeding programmes, where they transmit red colour as a single gene. The red trait in ‘Max Red Bartlett’, a mutant of ‘Bartlett’ (Synonym – ‘Williams Bon Chretien’), was mapped in Italy to linkage group 4 (LG4). At ARC Infruitec-Nietvoorbij, Stellenbosch, South Africa, ‘Bon Rouge’ pear, another red mutant of ‘Williams Bon Chretien’, was crossed with ‘Packham’s Triumph’ generating an F1 population with a segregation of (54:71) red:green, approximating to a 1:1 ratio; indicating a simple Mendelian inheritance of the red trait. The aim of the study was to determine if the ‘Bon Rouge’ red colour trait maps to approximately the same position as the ‘Max Red Bartlett’ red colour trait on LG4, and if so, to identify SSR markers that are mapped closer to the red colour trait than were previously reported. The seven published pear and apple SSR markers mapped in the appropriate region of LG4 in pear and in apple maps were identified and screened in the parents and, where informative, were scored in 125 seedlings for co-segregation analysis. Single locus segregations were checked with JoinMap 4.1 and this program was also used to generate a genetic map for LG4 of the ‘Bon Rouge’ x ‘Packham’s Triumph’ progeny using the SSR markers and the red locus. Two linkage maps were constructed at a LOD threshold of 3 using the Kosambi mapping function, one each with the maximum likelihood and regression mapping algorithms. The genetic linkage map of LG4 of ‘Bon Rouge’ x ‘Packham’s Triumph’ consisted of seven SSR markers (2 from apple and 5 from pear). Markers CH01d03 and CH02c02b were mapped on the same position as the red trait in ‘Max Red Bartlett’ reported by Dondini et al. (2008) and four more markers were added. One of the newly mapped markers, NH011a has been found to be closely linked to the red trait, with an approximate distance of 4 cM. This marker can be used to indirectly select for the red gene in pear, for example to distinguish heterozygotes from homozygotes. This work sets the scene for further genetic studies on the red trait in pear breeding programmes.
2

SSR-based genetic mapping of QTLs determining chilling requirements for time of initial vegetative budbreak in domesticated apple (Malus x domestica Borkh.) cultivar ‘Anna’ x ‘Austin’

Hove, Paidashe January 2012 (has links)
>Magister Scientiae - MSc / The Rosaceae family contains major temperate crops such as the domesticated apple(Malus x domestica Borkh.), peach (Prunus persica L. Batsch) and European pear (Pyrus communis L.). However, despite its evident economic importance, it is generally poorly studied in genomic terms, relative to the other major crop groups. Microsatellite and Diversity Array Technology (DArT) genetic markers have been exploited in this work and are essential tools in genetic map construction and marker-assisted selection (MAS) of high quality apples and other rosaceous crops. Microsatellites are advantageous in that they are co-dominant, highly polymorphic, abundant, transferable and reliably reproducible; hence their use in this study. In order for budbreak to take place in a timely and homogenous fashion, apple trees need a period of exposure to low temperatures.Within orchards the application of chemicals that induce budbreak in unsuitable environments is required to produce apples from cultivars that require high chilling levels. However, this and other practices using chemicals in orchards tend to pollute the environment. One of the solutions to this problem is to breed low chill apples such as ‘Anna’ cultivar, which was used as one of the parents in this study.This work was aimed at understanding the underlying genetic factors that determine chilling requirements for the time of initial vegetative budbreak trait in the apple cross ‘Anna’ x ‘Austin’. This was achieved through linkage map construction using SSR and DArT molecular markers followed by QTL analysis. This thesis has therefore exploited the large number of Expressed Sequence Tags (ESTs) and genome sequence data for the apple, using Tandem Repeats Finder, to design a total of 98 new SSR primers pairs. The other 369 SSR markers used in this work were from published work. JoinMap! 4.1 software was used to create an integrated genetic map with 17 linkage groups, for the domesticated apple cultivar, ‘Austin’ x ‘Anna’ mapping population with 80 individuals.The result of this process was a genetic map 1 212cM in length, and a total of 429 markers (314 DArT and 115 SSR), at an average density of a marker every 4 cM. This map was used identify the Quantitative Trait Loci (QTLs) determining chilling requirements for time of vegetative budbreak (IVB). In this process, putative IVB QTLs were identified in the ‘Anna’ x ‘Austin’ mapping population using the rMQM analysis function of MapQTL! 6.0, for both adult and seedling data collected over 3 growing seasons from 1996 to 1998. These QTLs were detected on linkage groups 2, 9 and 14,and explained 0.3 to 12.8 % of the observed phenotypic variation for the adult population,and 5.3 - 21 % for the seedling population. Seedling (LG 14) and adult (LGs 5, 7, 10) specific QTLs were also detected for the ‘Anna’ x ‘Austin’ cross. These QTLs will provide the basis for marker validation on related mapping populations in the apple breeding programme, and for the future identification of candidate genes controlling the process of budbreak.

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