3. Electronic Theses and Dissertations (ETDs) - All submissions
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Item Y-specific restriction fragment length polymorphisms In Southern African populations.(1992) Spurdle, Amanda BSeven Y chromosome probes and thirteen restriction enzyme digests were used to examine a conservative estimate of 20000bp, and no new Y-specific polymorphisms were revealed by these systems. The Y chromosome probe 49a, which reveals a Y-specific haplotype with TaqI, was shown to reveal five new complex polymorphisms with Bglll, Hindlll, Pst I, PvuII and Sstl. The new polymorphisms exhibit great genetic diversity, and each enzyme reveals numerous haplotypes, which mostly occur infrequently and are population-specific. The haplotypes for a given enzyme do not correlate strictly with those revealed by the other enzymes, including TaqI, suggesting that each polymorphism results from a combination of restriction site mutations and rearrangement events. Association between the different 49a polymorphisms occurs only in individuals of recent common genetic origin. Y-specific 49a/TagI haplotypes were determined for 933 individuals drawn from 23 different African populations. A total of 31 new haplotypes were observed, some of which contained new alleles or allelic variants. Duplication, in addition to CpG mutation, is implicated in the generation of certain allelic variants. Cluster analysis of genetic distances between populations was calculated using the 49a/TagI haplotype frequencies. Y-specific 49a/TagI haplotype analysis of individual populations was not sufficiently sensitive to accurately distinguish between the different Bantu-speaking Negroid tribal groups. Cluster analysis of larger groupings was more stable, and with the exception of the Khoisan, resulted in a basic split between African and non-African populations. The linkage disequilibrium of the XY275 MspI Y-linked polymorphism was determined. The high allele was generally found in association with the Y chromosome, but the Y-associated low allele was found to occur in Bantu-speaking Negroids, Khoisan-speaking Negroids, the Khoisan, two groups of mixed ancestry, and the Caucasoid South African Asiatic Indian population. The discovery of Y-associated low alleles in non-African as well as African populations suggests that more than one Y chromosome gave rise to the present-day non-African population. The pDP31/EcoRI, p21Al/TagI and Y Alu polymorphisms were also studied in several southern African populations. The pDP31 duplication occurred at high frequencies in Caucasoids, and could be used to indicate Caucasoid male gene flow into hybrid populations. The p21Al/TagI point mutation showed no distinct trends in frequency in the different populations, and several Taql mutations are proposed to have occurred in the repeat unit recognized by this sequence. The Y Alu polymorphism occurred infrequently in Caucasoids, at intermediate frequency in the Khoisan, and at high frequency in Negroids. The presence of the Y Alu insertion in all three major population groups studied is interpreted to suggest that the insert predates the diversification of Homo sapiens. The relationship between the different Y-linked polymorphisms was determined in the populations studied. The Y Alu polymorphism is believed to have originated once from sequencing data, but such information is not available for the other Y polymorphisms studied. No absolute relationship was observed between the Y Alu polymorphism and the 49a/TagI, XY275 Mspl, pDP31/£coRI and p21Al/TagI polymorphisms. It is suggested that the latter polymorphisms have arisen more than once.Item Y-chromosome variation in the South African 'coloured' population(2004) Motladiile, Thejane WilsonGenetic polymorphisms within the non-recombining portion of Y-chromosome (NRY) preserve a record of human paternal genetic heritage that has persisted to the present, allowing human evolutionary inference, population affinity and demographic history, to be elucidated. To elucidate the geographic origins of the paternal ancestry of the present- day South African (SA) ‘Coloured’ population, a total sample of 167 individuals consisting of Cape Malay (N=54) and ‘Coloured’ groups from Cape Town (N=48) and Johannesburg (N=65) were analysed at 21 binary and eight short tandem repeat (STR) polymorphic loci within NRY. A SA White sample (present study, N=97) as well as other presumed parental populations were included for comparative analysis. Haplotypes constructed using both biallelic haplogroup and STR haplotype data assisted in resolving the geographic regions of origin of Y-chromosome in these groups. Altogether the proportions of African, European and Asian contributions were estimated to be 0%, 18.5% and 46.3% in the Cape Malay, 31.3%, 25% and 20.1% in the Cape ‘Coloureds’, and 24.6%, 40% and 16.9%, in the ‘Coloured’ group from Johannesburg. Those haplotypes that could not be unambiguously resolved to European or Asian origins were referred to as Eurasian lineages, and constituted 35.2%, 22.9% and 18.5% of Y- chromosomes in the Cape Malays, Cape ‘Coloureds’ and Johannesburg ‘Coloureds’, respectively. While the ‘Coloured’ groups currently residing in Cape Town and Johannesburg were not significantly different from each other, both groups were significantly different from the Cape Malay population. This was further supported from the association of these groups in population trees. For the most part, these data corroborate historical data concerning the history of ‘Coloured’ populations, but is the first study to show how males have contributed in shaping the gene pool of the ‘Coloured’ population from South Africa.Item Phylogeography of Y chromosome haplogroups A & B in Africa(2015-04-22) Naidoo, ThijessenEvolution and historical events over the past 300 000 years have contributed in shaping the gene pool of sub-Saharan African populations. By examining patterns of Y chromosome variation, through the screening of single nucleotide polymorphisms (SNPs) and short tandem repeats (STRs), the present study aimed to characterise the phylogeography of ancient African Y chromosome haplogroups found in populations across sub-Saharan Africa, as well as understand the genetic affinities of these populations. In order to screen the large number of the markers required, seven multiplex single base extension assays were developed. These were used to refine the resolution of Y chromosomes commonly found in Africa, but also included a few markers to delineate the common non-African Y chromosome haplogroups, following a hierarchical screening process. In total, 1667 males were screened, and these data were compiled together with comparative published data. The resultant SNP and STR dataset was used in illustrating, more specifically, the phylogeographies of haplogroups A and B. The wide geographic distribution of haplogroup A, together with its position at the root of the phylogeny and high diversity, support an early diversification of the haplogroup into its subclades, which subsequently spread across Africa. The distribution of major haplogroup B subclades, however, are possibly due to post-glacial migrations in the case of haplogroup B-M112, and recent population expansions, leading to the common presence of haplogroup B-M152 across sub-Saharan Africa. The spread of haplogroup E, however, created the biggest impact on African populations; with its expansion likely resulting in the diminished presence of many of the subclades of haplogroups A and B. The Y chromosome compositions of present sub-Saharan African populations are, thus, the result of several diversification events, followed by migration, and mixing of population groups, over the course of modern human existence.