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The identification of chemical compounds that decrease cellular levels of toxic Huntington's disease protein through a novel cell-based assay

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dc.contributor.advisor David E. Housman. en_US
dc.contributor.author Coufal, Myra Alfert en_US
dc.contributor.other Massachusetts Institute of Technology. Dept. of Biology. en_US
dc.date.accessioned 2008-02-28T16:26:27Z
dc.date.available 2008-02-28T16:26:27Z
dc.date.copyright 2006 en_US
dc.date.issued 2006 en_US
dc.identifier.uri http://dspace.mit.edu/handle/1721.1/34622 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/34622
dc.description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2006. en_US
dc.description Vita. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract Huntington's disease (HD) is a progressive degenerative neurological disorder. Individuals who inherit the IT15 gene with an expansion of the CAG repeat region inevitably succumb to increasingly sever motor, psychological, and cognitive symptoms. I sought to develop an assay system with the capability for identification of chemical compounds that selectively decrease the intracellular levels of disease-causing expanded polyglutamine huntingtin (Htt) protein without reducing the intracellular levels of the potentially protective normal Htt. To achieve this goal I designed a cell-based assay using the enzymatic activity of E. coli [beta]-galactosidase as a reporter for Htt protein levels. I expressed either expanded (97Q) or normal (23Q) Htt fused to the [beta]-galactosidase alpha-subunit ([alpha]) in an inducible fashion in PC12 cells which also expressed the [beta]-galactosidase delta-subunit ([delta]). Complementation between these expressed subunits allowed the formation of functional P-galactosidase. The level of [beta]-galactosidase activity in these [delta]-[alpha]97Q and [delta]-[alpha]23Q cells directly correlated with the amount of a 97Q and a 23Q fusion protein levels, indicating that [beta]-galactosidase activity could be used as a reporter in this system for Htt protein levels. en_US
dc.description.abstract (cont.) I implemented this cell-based assay as a secondary assay to characterize a group of compounds that had been initially identified in a High Throughput Screen because they reduced levels of expanded Htt-fragment fused to GFP. Of the 34 compounds characterized in the -galactosidase [delta]-[alpha]97Q assay, dose response curves and counter-screening with [delta]-[alpha]23Q cells revealed that seven compounds decrease [beta]-galactosidase activity only in [delta]-[alpha]97Q cells. Immunofluorescence demonstrated that two compounds decrease levels of expanded but not normal Htt proteins in the cells. Finally, tests of toxicity on HttQ103 PC12 cell lines, which show specific toxicity following expression of expanded Htt, revealed a significant correlation with the results from the [beta]-galactosidase assay and the identification of at least one compound which continued to meet the criteria for therapeutic intervention in HD. These results support the feasibility of the development of an HD therapeutic strategy based on small molecules which cause a specific reduction of intracellular expanded Htt protein levels and suggest a program of development for such molecules. en_US
dc.description.statementofresponsibility by Myra Alfert Coufal. en_US
dc.format.extent 108 leaves 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/1721.1/34622 en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582
dc.subject Biology. en_US
dc.title The identification of chemical compounds that decrease cellular levels of toxic Huntington's disease protein through a novel cell-based assay en_US
dc.type Thesis en_US
dc.description.degree Ph.D. en_US
dc.contributor.department Massachusetts Institute of Technology. Dept. of Biology. en_US
dc.identifier.oclc 71331906 en_US


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