Evidence map›Paper›PMID 21081963›Full record

ReviewNature reviews. Molecular cell biology2010

The prion hypothesis: from biological anomaly to basic regulatory mechanism.

Mick F Tuite, Tricia R Serio

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

93 citing papers in PubMed, 150 citations in OpenAlex.

  1. Article
  2. Exposed Hsp70-binding site impacts yeast Sup35 prion disaggregation and propagation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Review
  4. Review
  5. Detecting anomalous proteins using deep representations.NAR genomics and bioinformatics · 2024
    Article
  6. Multiple aspects of amyloid dynamicsFrontiers in molecular neuroscience · 2024
    Article
  7. Synthesis and anti-prion aggregation activity of acylthiosemicarbazide analogues.Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  8. Article
  9. Measuring prion propagation in single bacteria elucidates a mechanism of loss.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Ribosomal RNA Modulates Aggregation of theInternational journal of molecular sciences · 2020
    Article
  20. Article

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Mick F TuiteKent Fungal Group, School of Biosciences, University of Kent, Canterbury, Kent CT2 7NJ, UK. M.F.Tuite@kent.ac.uk
Tricia R Serio
Brown University · USUniversity of Kent · GB

Funding

Prion Cycle Regulation In VivoR01GM069802 · NIGMS · UNIVERSITY OF ARIZONA · PI SERIO, TRICIA R. · 2006 to 2014
$2.7M
Biotechnology and Biological Sciences Research Council BB/H012982/1NIGMS NIH HHS R01 GM069802Wellcome Trust
6 · The paper itself

Abstract

Prions are unusual proteinaceous infectious agents that are typically associated with a class of fatal degenerative diseases of the mammalian brain. However, the discovery of fungal prions, which are not associated with disease, suggests that we must now consider the effect of these factors on basic cellular physiology in a different light. Fungal prions are epigenetic determinants that can alter a range of cellular processes, including metabolism and gene expression pathways, and these changes can lead to a range of prion-associated phenotypes. The mechanistic similarities between prion propagation in mammals and fungi suggest that prions are not a biological anomaly but instead could be a newly appreciated and perhaps ubiquitous regulatory mechanism.

Indexed as

Cell Physiological PhenomenaAnimalsEpigenesis, GeneticFungiGene Expression RegulationHumansModels, BiologicalPhenotypePrion DiseasesPrionsSignal TransductionPrions

Identifiers

PMID21081963
PMCPMC3003427
OpenAlexW1982935057

What OpenQuestion holds

Textmetadata
LicenceTDM
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.