Literature DB >> 11123686

The relationship between visible intracellular aggregates that appear after overexpression of Sup35 and the yeast prion-like elements [PSI(+)] and [PIN(+)].

P Zhou1, I L Derkatch, S W Liebman.   

Abstract

Overproduced fusions of Sup35 or its prion domain with green fluorescent protein (GFP) have previously been shown to form frequent dots in [PSI(+)] cells. Rare foci seen in [psi(-)] cells were hypothesized to indicate the de novo induction of [PSI(+)] caused by the overproduced prion domain. Here, we describe novel ring-type aggregates that also appear in [psi(-)] cultures upon Sup35 overproduction and show directly that dot and ring aggregates only appear in cells that have become [PSI(+)]. The formation of either type of aggregate requires [PIN(+)], an element needed for the induction of [PSI(+)]. Although aggregates are visible predominantly in stationary-phase cultures, [PSI(+)] induction starts in exponential phase, suggesting that much smaller aggregates can also propagate [PSI(+)]. Such small aggregates are probably present in [PSI(+)] cells and, upon Sup35-GFP overproduction, facilitate the frequent formation of dot aggregates, but only the occasional appearance of ring aggregates. In contrast, rings are very frequent when [PSI(+)] cultures, including those lacking [PIN(+)], are grown in the presence of GuHCl or excess Hsp104 while overexpressing Sup35-GFP. Thus, intermediates formed during [PSI(+)] curing seem to facilitate ring formation. Surprisingly, GuHCl and excess Hsp104, which are known to promote loss of [PSI(+)], did not prevent the de novo induction of [PSI(+)] by excess Sup35 in [psi(-)][PIN(+)] strains.

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Year:  2001        PMID: 11123686     DOI: 10.1046/j.1365-2958.2001.02224.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  77 in total

1.  Strains of [PSI(+)] are distinguished by their efficiencies of prion-mediated conformational conversion.

Authors:  S M Uptain; G J Sawicki; B Caughey; S Lindquist
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

2.  Interactions among prions and prion "strains" in yeast.

Authors:  Michael E Bradley; Herman K Edskes; Joo Y Hong; Reed B Wickner; Susan W Liebman
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-30       Impact factor: 11.205

Review 3.  Patterns of [PSI (+) ] aggregation allow insights into cellular organization of yeast prion aggregates.

Authors:  Jens Tyedmers
Journal:  Prion       Date:  2012-07-01       Impact factor: 3.931

4.  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

5.  Modulation of prion formation, aggregation, and toxicity by the actin cytoskeleton in yeast.

Authors:  Elena E Ganusova; Laura N Ozolins; Srishti Bhagat; Gary P Newnam; Renee D Wegrzyn; Michael Y Sherman; Yury O Chernoff
Journal:  Mol Cell Biol       Date:  2006-01       Impact factor: 4.272

6.  Analysis of Small Critical Regions of Swi1 Conferring Prion Formation, Maintenance, and Transmission.

Authors:  Stephanie Valtierra; Zhiqiang Du; Liming Li
Journal:  Mol Cell Biol       Date:  2017-09-26       Impact factor: 4.272

7.  The mechanisms of [URE3] prion elimination demonstrate that large aggregates of Ure2p are dead-end products.

Authors:  Leslie Ripaud; Laurent Maillet; Christophe Cullin
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

8.  Effects of Q/N-rich, polyQ, and non-polyQ amyloids on the de novo formation of the [PSI+] prion in yeast and aggregation of Sup35 in vitro.

Authors:  Irina L Derkatch; Susan M Uptain; Tiago F Outeiro; Rajaraman Krishnan; Susan L Lindquist; Susan W Liebman
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-23       Impact factor: 11.205

Review 9.  Hsp104 and prion propagation.

Authors:  Nina V Romanova; Yury O Chernoff
Journal:  Protein Pept Lett       Date:  2009       Impact factor: 1.890

Review 10.  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

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