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GENE EXPRESSION KINETICS AND PROTEIN DISTRIBUTION OF NUCLEOTIDE EXCISION REPAIR FACTORS IN THE INNER EAR AS A FUNCTION OF cis-DIAMMINEDICHLOROPLATINUM-II DNA DAMAGE

Guthrie, O'neil W. (2006) GENE EXPRESSION KINETICS AND PROTEIN DISTRIBUTION OF NUCLEOTIDE EXCISION REPAIR FACTORS IN THE INNER EAR AS A FUNCTION OF cis-DIAMMINEDICHLOROPLATINUM-II DNA DAMAGE. Doctoral Dissertation, University of Pittsburgh. (Unpublished)

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Abstract

The kinetics of the rate-limiting genes of the molecular DNA repair pathways of nucleotide excision repair (NER) were quantified from the inner ear as a function of cis-diamminedichloroplatinum-II (cisplatin) treatment. The distribution of the post-translational products of these genes was evaluated among neurons and sensory hair cells of the inner ear following cisplatin treatment. These NER factors (genes & post-translational products) are only potentiated by DNA damage and are particularly sensitive to cisplatin induced DNA damage. A 2 x 3 x 2 factorial design, consisting of two treatment conditions (saline and cisplatin treated Fischer344 rats), three survival times and two molecular analysis methods (polymerase chain reaction and immunohistochemistry) was employed in this dissertation. The results revealed at least five important findings. First, it revealed for the first time that complex DNA repair molecular pathways such as NER exist in the inner ear. Second, it revealed for the first time that molecules used by advanced tumor cells to detect and repair damaged DNA from cisplatin genotoxicity also generalize to the inner ear and are stimulated by even small sub-toxic doses of cisplatin. Third, it revealed for the first time that NER proteins reside in the cytoplasm of neurons under normal conditions and translocate to the nucleus under conditions of genomic stress. Fourth, it revealed for the first time that the basal coil of the mammalian cochlea differs from the apical coil in the magnitude and latency in which NER molecules translocate from the cytoplasm to the nucleus under conditions of genomic stress. Fifth, the current work provides the bases for a new line of hearing research focused on molecular mechanisms of inner ear DNA repair.


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Details

Item Type: University of Pittsburgh ETD
Status: Unpublished
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Guthrie, O'neil W.owg1@pitt.eduOWG1
ETD Committee:
TitleMemberEmail AddressPitt UsernameORCID
Committee ChairPalmer, Catherinepalmercv@upmc.eduCVP
Committee MemberBalaban, Careybalabancd@upmc.edu
Committee MemberDurrant, Johndurrant@pitt.eduDURRANT
Committee MemberPratt, Sheilaspratt@pitt.eduSPRATT
Date: 22 November 2006
Date Type: Completion
Defense Date: 25 August 2006
Approval Date: 22 November 2006
Submission Date: 10 November 2006
Access Restriction: No restriction; Release the ETD for access worldwide immediately.
Institution: University of Pittsburgh
Schools and Programs: School of Health and Rehabilitation Sciences > Communication Science and Disorders
Degree: PhD - Doctor of Philosophy
Thesis Type: Doctoral Dissertation
Refereed: Yes
Uncontrolled Keywords: audiology; DNA damage; DNA repair; molecular biology; ototoxicity; pharmacology
Other ID: http://etd.library.pitt.edu/ETD/available/etd-11102006-093242/, etd-11102006-093242
Date Deposited: 10 Nov 2011 20:04
Last Modified: 19 Dec 2016 14:37
URI: http://d-scholarship.pitt.edu/id/eprint/9619

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