Literature DB >> 18097160

Beer and bread to brains and beyond: can yeast cells teach us about neurodegenerative disease?

Aaron D Gitler1.   

Abstract

For millennia, humans have harnessed the astonishing power of yeast, producing such culinary masterpieces as bread, beer and wine. Therefore, in this new millennium, is it very farfetched to ask if we can also use yeast to unlock some of the modern day mysteries of human disease? Remarkably, these seemingly simple cells possess most of the same basic cellular machinery as the neurons in the brain. We and others have been using the baker's yeast, Saccharomyces cerevisiae, as a model system to study the mechanisms of devastating neurodegenerative diseases such as Parkinson's, Huntington's, Alzheimer's and amyotrophic lateral sclerosis. While very different in their pathophysiology, they are collectively referred to as protein-misfolding disorders because of the presence of misfolded and aggregated forms of various proteins in the brains of affected individuals. Using yeast genetics and the latest high-throughput screening technologies, we have identified some of the potential causes underpinning these disorders and discovered conserved genes that have proven effective in preventing neuron loss in animal models. Thus, these genes represent new potential drug targets. In this review, I highlight recent work investigating mechanisms of cellular toxicity in a yeast Parkinson's disease model and discuss how similar approaches are being applied to additional neurodegenerative diseases.

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Year:  2007        PMID: 18097160     DOI: 10.1159/000109759

Source DB:  PubMed          Journal:  Neurosignals        ISSN: 1424-862X


  23 in total

Review 1.  Polyglutamine misfolding in yeast: toxic and protective aggregation.

Authors:  Martin L Duennwald
Journal:  Prion       Date:  2011-10-01       Impact factor: 3.931

Review 2.  The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease.

Authors:  Oliver D King; Aaron D Gitler; James Shorter
Journal:  Brain Res       Date:  2012-01-21       Impact factor: 3.252

3.  Profilin 1 associates with stress granules and ALS-linked mutations alter stress granule dynamics.

Authors:  Matthew D Figley; Gregor Bieri; Regina-Maria Kolaitis; J Paul Taylor; Aaron D Gitler
Journal:  J Neurosci       Date:  2014-06-11       Impact factor: 6.167

Review 4.  TDP-43 toxicity in yeast.

Authors:  Maria Armakola; Michael P Hart; Aaron D Gitler
Journal:  Methods       Date:  2010-11-27       Impact factor: 3.608

5.  Growth assays to assess polyglutamine toxicity in yeast.

Authors:  Martin L Duennwald
Journal:  J Vis Exp       Date:  2012-03-05       Impact factor: 1.355

Review 6.  RNA-binding proteins with prion-like domains in ALS and FTLD-U.

Authors:  Aaron D Gitler; James Shorter
Journal:  Prion       Date:  2011-07-01       Impact factor: 3.931

7.  High-throughput yeast plasmid overexpression screen.

Authors:  Michael S Fleming; Aaron D Gitler
Journal:  J Vis Exp       Date:  2011-07-27       Impact factor: 1.355

Review 8.  RNA-binding proteins with prion-like domains in health and disease.

Authors:  Alice Ford Harrison; James Shorter
Journal:  Biochem J       Date:  2017-04-07       Impact factor: 3.857

9.  A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity.

Authors:  Brian S Johnson; J Michael McCaffery; Susan Lindquist; Aaron D Gitler
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-23       Impact factor: 11.205

10.  Reversing deleterious protein aggregation with re-engineered protein disaggregases.

Authors:  Meredith E Jackrel; James Shorter
Journal:  Cell Cycle       Date:  2014-04-02       Impact factor: 4.534

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