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Permanent link (DOI): https://doi.org/10.7939/R35H7C253

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The Prion Protein: Modulation of Potassium Channels and a Novel Mouse Model of a Disease-Causing Hydrophobic Domain Insertion Mutation Open Access

Descriptions

Other title
Subject/Keyword
Gerstmann-Sträussler-Schienker
Potassium Channel
Prion
Neurodegeneration
Type of item
Thesis
Degree grantor
University of Alberta
Author or creator
Mercer, Robert Corrigan Curtis
Supervisor and department
Westaway, David (Medicine)
Examining committee member and department
Casey, Joe (Biochemistry)
Young, Howard (Biochemistry)
Holmes, Charles (Biochemistry)
Telling, Glenn (Microbiology, Immunology and Pathology, Colorado State University)
Department
Department of Medicine
Specialization
Experimental Medicine
Date accepted
2016-02-01T13:33:18Z
Graduation date
2016-06
Degree
Doctor of Philosophy
Degree level
Doctoral
Abstract
Prion diseases are invariably fatal neurodegenerative diseases of humans and other mammals. While they can manifest as sporadic, infectious or genetic etiologies, the central event in prion disease is the structural conversion of the prion protein (PrPC) to an alternative conformer PrPSc. PrP is a highly enigmatic molecule with a wide range of proposed functions and disease associated phenotypes. A molecular understanding of the physiological function of PrP and the pathological characteristics of PrPSc is essential to uncover the means by which these diseases may be combatted. Herein, I describe two sets of analysis: i) the consequences of the physiological interaction between PrP and a potassium channel modulating protein, dipeptidyl aminopeptidase-like protein 6 (DPP6) and ii) the characterization of a novel mouse model of a genetic form of prion disease, Gerstmann–Sträussler–Scheinker disease (GSS). i) PrP, in a DPP6 dependent manner, enhances the properties of Kv4.2 voltage gated potassium channels such that there is an increase in peak amplitude, a rightward shift of the voltage-dependent steady-state inactivation curve, a slower inactivation, and a faster recovery from steady-state inactivation. ii) A patient presenting with GSS was found to harbor a novel insertion mutation of the hydrophobic domain of PrP. We created transgenic mice expressing this allele and present a biochemical and histopathological workup of these animals. They recapitulate many of the features of GSS, in particular a defining low molecular weight proteinase K resistant fragment of the prion protein. Brain extracts of affected animals can be used to accelerate disease in mice expressing the same insertion allele but wild type mice are refractory to this treatment.
Language
English
DOI
doi:10.7939/R35H7C253
Rights
This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for the purpose of private, scholarly or scientific research. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
Citation for previous publication
Mercer, R.C., Ma, L., Watts, J.C., Strome, R., Wohlgemuth, S., Yang, J., Cashman, N.R., Coulthart, M.B., Schmitt-Ulms, G., Jhamandas, J.H. and Westaway, D., 2013. The prion protein modulates A-type K+ currents mediated by Kv4. 2 complexes through dipeptidyl aminopeptidase-like protein 6. Journal of Biological Chemistry, 288(52), pp.37241-37255.

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