Evidence map›Paper›PMID 21379326›Full record

ArticlePLoS genetics2011

[SWI], the prion formed by the chromatin remodeling factor Swi1, is highly sensitive to alterations in Hsp70 chaperone system activity.

Justin K Hines, Xiaomo Li, Zhiqiang Du, Takashi Higurashi, Liming Li, Elizabeth A Craig

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 68 citations in OpenAlex.

  1. Human proteins curing yeast prions.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  2. Article
  3. Article
  4. Differential Interactions of Molecular Chaperones and Yeast Prions.Journal of fungi (Basel, Switzerland) · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. How Do Yeast Cells Contend with Prions?International journal of molecular sciences · 2020
    Review
  10. The metastable states of proteins.Protein science : a publication of the Protein Society · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
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  19. Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Justin K HinesDepartment of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Xiaomo Li
Zhiqiang Du
Takashi Higurashi
Liming Li
Elizabeth A Craig
Northwestern University · USUniversity of Wisconsin–Madison · US

Funding

MRNA DEGRADATION AND TRANSLATION CONTROL IN YEASTR01GM053655 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI JOHNSON, ARLEN W · 1995 to 2017
$5.1M
REGULATION AND FUNCTION OF THE YEAST HEAT SHOCK RESPONSER01GM031107 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI CRAIG, ELIZABETH A · 1985 to 2012
$1.9M
Elucidating the Relations of Heat Shock Factors, Molecular Chaperones and PrionsR01NS056086 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LI, LIMING · 2008 to 2012
$1.8M
NIGMS NIH HHS GM53655NIGMS NIH HHS GM846542NIGMS NIH HHS R01 GM031107NIGMS NIH HHS R01 GM053655NINDS NIH HHS NS056086NINDS NIH HHS R01 NS056086
6 · The paper itself

Abstract

The yeast prion [SWI+], formed of heritable amyloid aggregates of the Swi1 protein, results in a partial loss of function of the SWI/SNF chromatin-remodeling complex, required for the regulation of a diverse set of genes. Our genetic analysis revealed that [SWI+] propagation is highly dependent upon the action of members of the Hsp70 molecular chaperone system, specifically the Hsp70 Ssa, two of its J-protein co-chaperones, Sis1 and Ydj1, and the nucleotide exchange factors of the Hsp110 family (Sse1/2). Notably, while all yeast prions tested thus far require Sis1, [SWI+] is the only one known to require the activity of Ydj1, the most abundant J-protein in yeast. The C-terminal region of Ydj1, which contains the client protein interaction domain, is required for [SWI+] propagation. However, Ydj1 is not unique in this regard, as another, closely related J-protein, Apj1, can substitute for it when expressed at a level approaching that of Ydj1. While dependent upon Ydj1 and Sis1 for propagation, [SWI+] is also highly sensitive to overexpression of both J-proteins. However, this increased prion-loss requires only the highly conserved 70 amino acid J-domain, which serves to stimulate the ATPase activity of Hsp70 and thus to stabilize its interaction with client protein. Overexpression of the J-domain from Sis1, Ydj1, or Apj1 is sufficient to destabilize [SWI+]. In addition, [SWI+] is lost upon overexpression of Sse nucleotide exchange factors, which act to destabilize Hsp70's interaction with client proteins. Given the plethora of genes affected by the activity of the SWI/SNF chromatin-remodeling complex, it is possible that this sensitivity of [SWI+] to the activity of Hsp70 chaperone machinery may serve a regulatory role, keeping this prion in an easily-lost, meta-stable state. Such sensitivity may provide a means to reach an optimal balance of phenotypic diversity within a cell population to better adapt to stressful environments.

Indexed as

Chromatin Assembly and DisassemblyAmino Acid SubstitutionChromosomal Proteins, Non-HistoneGene DeletionHeat-Shock ResponseHSP110 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsPrionsProtein Structure, TertiarySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTemperatureTranscription FactorsChromosomal Proteins, Non-HistoneHSP110 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsPrionsSaccharomyces cerevisiae ProteinsSWI1 protein, S cerevisiaeTranscription Factors

Identifiers

PMID21379326
PMCPMC3040656
OpenAlexW1997822902

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.