Protein misfolding toxicity and inclusion formation in cellular models of neurodegeneration
type: CreativeWork
description: Protein misfolding characterizes most neurodegenerative diseases. Protein misfolding is the conversion of specific proteins from their normal, often soluble, and native three-dimensional conformation into an aberrant, often insoluble, non-functional conformation. Protein inclusions and aggregates are among the major pathological hallmarks of protein misfolding associated with many neurodegenerative diseases. Yet, the role of aggregates and inclusions is not clearly defined and heavily debated. This study utilizes powerful genetic approaches in yeast and verification in mammalian neuronal cell lines to address the misfolding and toxicity of three proteins, the Rho Guanine Nucleotide Exchange Factor (RGNEF), Matrin3, which are involved in amyotrophic lateral sclerosis (ALS) and polyglutamine (polyQ) expanded huntingtin, which causes Huntington’s disease (HD). Genetic, biochemical, and pathological findings implicate RGNEF and Matrin3 in Amyotrophic Lateral Sclerosis (ALS). In this thesis we establish two novel humanized yeast models to study RGNEF and Matrin3. We find that RGNEF is toxic in yeast and can misfold and form inclusions. We also identify a potential new role for RGNEF as a microtubule regulator. Similarly, Matrin3 is also toxic and forms inclusions in yeast. We identify members of the Hsp90 and Hsp70 cytosolic chaperoning machinery as potent determinants of Matrin3 associated toxicity and misfolding and verify our findings in neuronal cell lines. Also, polyQ expanded repeats of the huntingtin protein are the sole known cause of Huntington’s disease (HD). We address the nexus of aging and aggregation, and toxicity of polyQ expanded repeats in a yeast model of aging. Aging is the most significant risk factor for all neurodegeneration, and we find that polyQ toxicity is exacerbated in aged cells while aggregates are lost. We also demonstrate that treating cells expressing polyQ with the steroidal lactone Withaferin A (WA) reduces toxicity while increasing agg…
abstract: Protein misfolding characterizes most neurodegenerative diseases. Protein misfolding is the conversion of specific proteins from their normal, often soluble, and native three-dimensional conformation into an aberrant, often insoluble, non-functional conformation. Protein inclusions and aggregates are among the major pathological hallmarks of protein misfolding associated with many neurodegenerative diseases. Yet, the role of aggregates and inclusions is not clearly defined and heavily debated. This study utilizes powerful genetic approaches in yeast and verification in mammalian neuronal cell lines to address the misfolding and toxicity of three proteins, the Rho Guanine Nucleotide Exchange Factor (RGNEF), Matrin3, which are involved in amyotrophic lateral sclerosis (ALS) and polyglutamine (polyQ) expanded huntingtin, which causes Huntington’s disease (HD). Genetic, biochemical, and pathological findings implicate RGNEF and Matrin3 in Amyotrophic Lateral Sclerosis (ALS). In this thesis we establish two novel humanized yeast models to study RGNEF and Matrin3. We find that RGNEF is toxic in yeast and can misfold and form inclusions. We also identify a potential new role for RGNEF as a microtubule regulator. Similarly, Matrin3 is also toxic and forms inclusions in yeast. We identify members of the Hsp90 and Hsp70 cytosolic chaperoning machinery as potent determinants of Matrin3 associated toxicity and misfolding and verify our findings in neuronal cell lines. Also, polyQ expanded repeats of the huntingtin protein are the sole known cause of Huntington’s disease (HD). We address the nexus of aging and aggregation, and toxicity of polyQ expanded repeats in a yeast model of aging. Aging is the most significant risk factor for all neurodegeneration, and we find that polyQ toxicity is exacerbated in aged cells while aggregates are lost. We also demonstrate that treating cells expressing polyQ with the steroidal lactone Withaferin A (WA) reduces toxicity while increasing agg…
author: Di Gregorio, Sonja E
language: en_ca
keywords: Protein misfolding, Neurodegeneration, Amyotrophic Lateral Sclerosis, Huntington’s Disease, RGNEF, Matrin3, PolyQ huntingtin, Hsp90, Sti1, Ydj1, DnajA1, Aging, Withaferin A, protein aggregation, protein inclusions
date published: 2021-04-21
date modified: 2026-07-27T21:56:18Z
provider: Western University
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: The University of Western Ontario

PropertyValue
property ID: Handle
value: https://hdl.handle.net/20.500.14721/31031