Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.598628
Title: The role of Ku in retrotransposition in Saccharomyces cerevisiae
Author: Downs, J.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 1999
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Abstract:
In order to determine whether the mobility of transposable elements is affected by Ku, a genetic system using the Tyl retrotransposon in Saccharomyces cerevisiae was used. Phenotypic analysis of yeast strains containing a null mutation of either subunit of Ku showed that Tyl retrotransposition rates were markedly reduced compared to wild-type cells. This phenotype appears to be specific to mutations in Ku, as strains with mutations in other DNA repair proteins were analysed and no significant effect on retrotransposition was observed. Biochemical techniques were employed to determine the stage of the retrotransposon life-cycle at which Ku was acting to facilitate the process. It has been determined that transcription, translation, and reverse transcription of the retroelement and element-encoded proteins are unaffected by the absence of Ku. Furthermore, there is no defect in proteolytic processing of a precursor fusion protein, retrotransposon virus-like particle assembly, or reverse transcriptase activity in the absence of Ku. Examination of another retrotransposon shows that same phenotype in the absence of Ku, suggesting that the mechanism by which Ku is facilitating retrotransposition is a general one, and not likely to be via targeting the integration machinery to specific regions of the genome. Ku was demonstrated to co-fractionate with the virus-like particles during purification, and immunoprecipitation experiments using antibodies directed at one of the Ku subunits demonstrate an interaction with the retrotransposon cDNA and integrase, but not the reverse transcriptase. Ku has previously been shown to bind to DNA double-strand ends in vitro, so one model by which Ku could facilitate retrotransposition is by binding to the cDNA ends and protecting them from nuclease-mediated degradation. However, examination of purified cDNA from wild-type and yku70 mutant strains shows no difference in the amount or integrity of DNA.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.598628  DOI: Not available
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