Evidence map›Paper›PMID 30153247›Full record

ArticlePLoS biology2018

Protein aggregates encode epigenetic memory of stressful encounters in individual Escherichia coli cells.

Sander K Govers, Julien Mortier, Antoine Adam, Abram Aertsen

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

79 citing papers in PubMed, 124 citations in OpenAlex.

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  13. TrackRefiner a tool for refinement of bacillus cell tracking data.NPJ systems biology and applications · 2025
    Article
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  15. Engineering Spatial Control of Bacterial Organelles.bioRxiv : the preprint server for biology · 2025
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Sander K GoversKU Leuven, Department of Microbial and Molecular Systems, Leuven, Belgium.
Julien MortierKU Leuven, Department of Microbial and Molecular Systems, Leuven, Belgium.
Antoine AdamKU Leuven, Department of Computer Science, Leuven, Belgium.
Abram AertsenKU Leuven, Department of Microbial and Molecular Systems, Leuven, Belgium.ORCID 0000-0002-1897-2305
KU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein misfolding and aggregation are typically perceived as inevitable and detrimental processes tied to a stress- or age-associated decline in cellular proteostasis. A careful reassessment of this paradigm in the E. coli model bacterium revealed that the emergence of intracellular protein aggregates (PAs) was not related to cellular aging but closely linked to sublethal proteotoxic stresses such as exposure to heat, peroxide, and the antibiotic streptomycin. After removal of the proteotoxic stress and resumption of cellular proliferation, the polarly deposited PA was subjected to limited disaggregation and therefore became asymmetrically inherited for a large number of generations. Many generations after the original PA-inducing stress, the cells inheriting this ancestral PA displayed a significantly increased heat resistance compared to their isogenic, PA-free siblings. This PA-mediated inheritance of heat resistance could be reproduced with a conditionally expressed, intracellular PA consisting of an inert, aggregation-prone mutant protein, validating the role of PAs in increasing resistance and indicating that the resistance-conferring mechanism does not depend on the origin of the PA. Moreover, PAs were found to confer robustness to other proteotoxic stresses, as imposed by reactive oxygen species or streptomycin exposure, suggesting a broad protective effect. Our findings therefore reveal the potential of intracellular PAs to serve as long-term epigenetically inheritable and functional memory elements, physically referring to a previous cellular insult that occurred many generations ago and meanwhile improving robustness to a subsequent proteotoxic stress. The latter is presumably accomplished through the PA-mediated asymmetric inheritance of protein quality control components leading to their specific enrichment in PA-bearing cells.

Indexed as

Epigenesis, GeneticAdaptation, PhysiologicalAnti-Bacterial AgentsEscherichia coliEscherichia coli ProteinsGene ExpressionGenes, ReporterGreen Fluorescent ProteinsHeat-Shock ProteinsHot TemperatureHydrogen PeroxideLuminescent ProteinsProtein AggregatesProtein FoldingProteostasisRed Fluorescent ProteinAnti-Bacterial AgentsEscherichia coli ProteinsGreen Fluorescent ProteinsHeat-Shock ProteinsHydrogen PeroxideIbpA protein, E coliLuminescent ProteinsProtein AggregatesRed Fluorescent ProteinStreptomycin

Identifiers

PMID30153247
PMCPMC6112618
OpenAlexW2889285236

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.