Yeast models of neurodegenerative diseases

MF Tuite - Progress in molecular biology and translational …, 2019 - Elsevier
The yeast Saccharomyces cerevisiae has been used to develop a wide range of highly
tractable living models of the major human neurodegenerative diseases. Yet even though …

Tumor suppressor protein p53 expressed in yeast can remain diffuse, form a prion, or form unstable liquid-like droplets

SK Park, S Park, C Pentek, SW Liebman - Iscience, 2021 - cell.com
Mutations in the p53 tumor suppressor are frequent causes of cancer. Because p53
aggregates appear in some tumor cells, it has been suggested that p53 could also cause …

Use of ade1 and ade2 mutations for development of a versatile red/white colour assay of amyloid‐induced oxidative stress in saccharomyces cerevisiae

V Bharathi, A Girdhar, A Prasad, M Verma, V Taneja… - Yeast, 2016 - Wiley Online Library
Mutations in adenine biosynthesis pathway genes ADE1 and ADE2 have been
conventionally used to score for prion [PSI+] in yeast. If ade1‐14 mutant allele is present …

Investigating the physiological response of Pichia (Komagataella) pastoris GS115 to the heterologous expression of misfolded proteins using chemostat cultures

AR Hesketh, JI Castrillo, T Sawyer, DB Archer… - Applied microbiology …, 2013 - Springer
Pichia pastoris is widely used as a host system for heterologous protein expression in both
academia and industry. Production is typically accomplished by a fed-batch induction …

MIL-CELL: a tool for multi-scale simulation of yeast replication and prion transmission

D Hall - European Biophysics Journal, 2023 - Springer
The single-celled baker's yeast, Saccharomyces cerevisiae, can sustain a number of
amyloid-based prions, the three most prominent examples being [URE3],[PSI+], and [PIN+] …

Probing the role of structural features of mouse PrP in yeast by expression as Sup35-PrP fusions

L Jossé, R Marchante, J Zenthon, T von der Haar… - Prion, 2012 - Taylor & Francis
The yeast Saccharomyces cerevisiae is a tractable model organism in which both to explore
the molecular mechanisms underlying the generation of disease-associated protein …

Discovery of arginine ethyl ester as polyglutamine aggregation inhibitor: conformational transitioning of huntingtin N-terminus augments aggregation suppression

V Singh, KA Patel, RK Sharma, PR Patil… - ACS chemical …, 2019 - ACS Publications
Huntington's disease (HD) is a genetic disorder caused by a CAG expansion mutation in the
huntingtin gene leading to polyglutamine (polyQ) expansion in the N-terminal part of …

[PSI+] turns 50

MF Tuite, GL Staniforth, BS Cox - Prion, 2015 - Taylor & Francis
abstract The year 2015 sees the fiftieth anniversary of the publication of a research paper
that underpins much of our understanding of fungal prion biology, namely “ψ, a cytoplasmic …

Aggregation dynamics and identification of aggregation-prone mutants of the von Hippel–Lindau tumor suppressor protein

X Le Goff, F Chesnel, O Delalande… - Journal of Cell …, 2016 - journals.biologists.com
Quality control mechanisms promote aggregation and degradation of misfolded proteins. In
budding yeast, the human von Hippel–Lindau protein (pVHL, officially known as VHL) is …

Characterization of aggregate load and pattern in living yeast cells by flow cytometry

IH Hidalgo, T Fleming, V Eckstein, S Herzig… - …, 2016 - Taylor & Francis
Protein aggregation is both a hallmark of and a driving force for a number of diseases. It is
therefore important to identify the nature of these aggregates and the mechanism (s) by …