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Response of DNA repair and replication systems to exocyclic nucleic acid base damage

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dc.contributor.advisor John M. Essigmann. en_US
dc.contributor.author Śrīvāstava, Nidhi en_US
dc.contributor.other Massachusetts Institute of Technology. Dept. of Biological Engineering. en_US
dc.date.accessioned 2012-07-02T15:43:38Z
dc.date.available 2012-07-02T15:43:38Z
dc.date.copyright 2012 en_US
dc.date.issued 2012 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/71468
dc.description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biological Engineering, 2012. en_US
dc.description Cataloged from PDF version of thesis. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract Genomes experience an often hostile environment that creates a vast array of damages that can give rise to myriad biological outcomes. Fortunately, cells are equipped with networks such as direct reversal, base excision repair, nucleotide excision repair, homologous recombination, and translesion synthesis that help preserve informational integrity. The first part of this dissertation focuses on whether or not bulky alkyl lesions at the N2 atom of guanine are addressed in vivo by the DinB bypass polymerase. In the work described herein, a collection of N2-guanine lesions was inserted in single-stranded M13 genomes and evaluated in strains possessing or lacking DinB via the competitive replication and adduct bypass (CRAB) and restriction endonuclease and postlabeling (REAP) assays. It was found that DinB could in fact bypass the N2-furfuryl-guanine lesion and its saturated homolog in vivo. The second part of this work describes how we systematically investigated the role that the distance from an origin of replication may have in the mutagenesis of an adduct. Our hypothesis was that a lesion farther from the origin of replication would be less mutagenic since it would be afforded more time for detection and removal before the replicative polymerase traversed it, fixing the mutation. We inserted 0-methylguanine in single-stranded M13 genomes at different distances from the origin of replication and analyzed progeny phage by the REAP assay. Our findings were in contrast with the hypothesis; a higher mutation frequency was obtained at the site distal from the origin of replication. Alternative hypotheses and future experiments are discussed as part of this work. The third part of this dissertation seeks to expand the spectrum of known substrates for the enzyme AIkB, which mediates direct reversal of DNA damage. AlkB is an iron- and CCketoglutarate- dependent dioxygenase that is part of the adaptive response in E. coli, and has homologs in many species. On basis of in vitro data we created the hypothesis that the N 2 guanine lesions as well as 6-methyladenine would be substrates for the enzyme AlkB in vivo. We found, however, in this case the in vitro results did not predict the biology observed in cells. en_US
dc.description.statementofresponsibility by Nidhi Shrivastav. en_US
dc.format.extent 201, 4524-4527, 8 p. en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582 en_US
dc.subject Biological Engineering. en_US
dc.title Response of DNA repair and replication systems to exocyclic nucleic acid base damage en_US
dc.title.alternative Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage en_US
dc.type Thesis en_US
dc.description.degree Ph.D. en_US
dc.contributor.department Massachusetts Institute of Technology. Dept. of Biological Engineering. en_US
dc.identifier.oclc 795194172 en_US


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