Prions, prionoids and protein misfolding disorders

C Scheckel, A Aguzzi - Nature Reviews Genetics, 2018 - nature.com
Prion diseases are progressive, incurable and fatal neurodegenerative conditions. The term
'prion'was first nominated to express the revolutionary concept that a protein could be …

Prions in yeast

SW Liebman, YO Chernoff - Genetics, 2012 - academic.oup.com
The concept of a prion as an infectious self-propagating protein isoform was initially
proposed to explain certain mammalian diseases. It is now clear that yeast also has …

Aneuploidy causes proteotoxic stress in yeast

AB Oromendia, SE Dodgson, A Amon - Genes & development, 2012 - genesdev.cshlp.org
Gains or losses of entire chromosomes lead to aneuploidy, a condition tolerated poorly in all
eukaryotes analyzed to date. How aneuploidy affects organismal and cellular physiology is …

Asymmetric segregation of protein aggregates is associated with cellular aging and rejuvenation

AB Lindner, R Madden, A Demarez… - Proceedings of the …, 2008 - National Acad Sciences
Aging, defined as a decrease in reproduction rate with age, is a fundamental characteristic
of all living organisms down to bacteria. Yet we know little about the causal molecular …

The physical basis of how prion conformations determine strain phenotypes

M Tanaka, SR Collins, BH Toyama, JS Weissman - Nature, 2006 - nature.com
A principle that has emerged from studies of protein aggregation is that proteins typically can
misfold into a range of different aggregated forms. Moreover, the phenotypic and …

Protein rescue from aggregates by powerful molecular chaperone machines

SM Doyle, O Genest, S Wickner - Nature reviews Molecular cell biology, 2013 - nature.com
Protein quality control within the cell requires the interplay of many molecular chaperones
and proteases. When this quality control system is disrupted, polypeptides follow pathways …

Mechanism of prion propagation: amyloid growth occurs by monomer addition

SR Collins, A Douglass, RD Vale, JS Weissman - PLoS biology, 2004 - journals.plos.org
Abundant nonfibrillar oligomeric intermediates are a common feature of amyloid formation,
and these oligomers, rather than the final fibers, have been suggested to be the toxic …

Molecular chaperones: a double-edged sword in neurodegenerative diseases

J Tittelmeier, E Nachman… - Frontiers in aging …, 2020 - frontiersin.org
Aberrant accumulation of misfolded proteins into amyloid deposits is a hallmark in many age-
related neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's …

Luminidependens (LD) is an Arabidopsis protein with prion behavior

S Chakrabortee, C Kayatekin… - Proceedings of the …, 2016 - National Acad Sciences
Prion proteins provide a unique mode of biochemical memory through self-perpetuating
changes in protein conformation and function. They have been studied in fungi and …

Prion switching in response to environmental stress

J Tyedmers, ML Madariaga, S Lindquist - PLoS biology, 2008 - journals.plos.org
Evolution depends on the manner in which genetic variation is translated into new
phenotypes. There has been much debate about whether organisms might have specific …