Literature DB >> 16793280

How to find a prion: [URE3], [PSI+] and [beta].

Reed B Wickner1, Herman K Edskes, Frank Shewmaker.   

Abstract

Infectious proteins (prions) in yeast or other microorganisms can be identified by genetic methods of rather general applicability. Infection in yeast means transfer by cytoplasmic mixing (cytoduction), a property of all non-chromosomal genetic elements whether plasmids, viruses, or prions. Prions can be diagnosed by reversible curability, increased occurrence when the corresponding protein is overproduced, a requirement for the gene for the corresponding protein for propagation, and, in some cases, similarity of phenotype of: (a) mutations in the gene for the protein and (b) the presence of the prion. This approach is illustrated with [URE3], an amyloid-based prion of the regulator of nitrogen catabolism, Ure2p and [PSI(+)] as a prion of the translation termination factor Sup35p. The prion concept is not limited to infectious amyloids, but includes proteins whose active form is necessary for the activation of the inactive precursor. We detail methods used in studies of [URE3] and [beta], a self-activating protease, some of which are of broad application.

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Year:  2006        PMID: 16793280     DOI: 10.1016/j.ymeth.2006.04.009

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  11 in total

1.  The Paf1 complex subunit Rtf1 buffers cells against the toxic effects of [PSI+] and defects in Rkr1-dependent protein quality control in Saccharomyces cerevisiae.

Authors:  Kristin M Klucevsek; Mary A Braun; Karen M Arndt
Journal:  Genetics       Date:  2012-05-17       Impact factor: 4.562

2.  Curing of the [URE3] prion by Btn2p, a Batten disease-related protein.

Authors:  Dmitry S Kryndushkin; Frank Shewmaker; Reed B Wickner
Journal:  EMBO J       Date:  2008-10-02       Impact factor: 11.598

3.  Protein-only mechanism induces self-perpetuating changes in the activity of neuronal Aplysia cytoplasmic polyadenylation element binding protein (CPEB).

Authors:  Sven U Heinrich; Susan Lindquist
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-26       Impact factor: 11.205

4.  High-throughput Screening for Protein-based Inheritance in S. cerevisiae.

Authors:  James S Byers; Daniel F Jarosz
Journal:  J Vis Exp       Date:  2017-08-08       Impact factor: 1.355

5.  A Prion Epigenetic Switch Establishes an Active Chromatin State.

Authors:  Zachary H Harvey; Anupam K Chakravarty; Raymond A Futia; Daniel F Jarosz
Journal:  Cell       Date:  2020-02-27       Impact factor: 41.582

6.  FUS/TLS forms cytoplasmic aggregates, inhibits cell growth and interacts with TDP-43 in a yeast model of amyotrophic lateral sclerosis.

Authors:  Dmitry Kryndushkin; Reed B Wickner; Frank Shewmaker
Journal:  Protein Cell       Date:  2011-03-30       Impact factor: 14.870

7.  Intrinsically Disordered Proteins Drive Emergence and Inheritance of Biological Traits.

Authors:  Sohini Chakrabortee; James S Byers; Sandra Jones; David M Garcia; Bhupinder Bhullar; Amelia Chang; Richard She; Laura Lee; Brayon Fremin; Susan Lindquist; Daniel F Jarosz
Journal:  Cell       Date:  2016-09-29       Impact factor: 41.582

Review 8.  Prion-like propagation of cytosolic protein aggregates: insights from cell culture models.

Authors:  Carmen Krammer; Hermann M Schätzl; Ina Vorberg
Journal:  Prion       Date:  2009-10-04       Impact factor: 3.931

Review 9.  Application of GFP-labeling to study prions in yeast.

Authors:  Lois E Greene; Yang-Nim Park; Daniel C Masison; Evan Eisenberg
Journal:  Protein Pept Lett       Date:  2009       Impact factor: 1.890

10.  The cellular concentration of the yeast Ure2p prion protein affects its propagation as a prion.

Authors:  Myriam Crapeau; Christelle Marchal; Christophe Cullin; Laurent Maillet
Journal:  Mol Biol Cell       Date:  2009-02-18       Impact factor: 4.138

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