Evidence map›Paper›PMID 40490499›Full record

ArticleMolecular systems biology2025

A transient mutational burst occurs during yeast colony development.

Nicolas Agier, Nina Vittorelli, Louis Ollivier, Frédéric Chaux, Alexandre Gillet-Markowska, Samuel O'Donnell, Fanny Pouyet, Gilles Fischer, Stéphane Delmas

Abstract read
In one paragraph

Article in Molecular systems biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

9 authors.

Nicolas AgierSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.ORCID http://orcid.org/0000-0003-2306-3138
Nina VittorelliSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.ORCID http://orcid.org/0009-0007-7359-6625
Louis OllivierSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.ORCID http://orcid.org/0000-0003-1177-6202
Frédéric ChauxSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.
Alexandre Gillet-MarkowskaSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.
Samuel O'DonnellSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.
Fanny PouyetSorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France.ORCID http://orcid.org/0000-0001-5614-6998
Gilles Fischer *Sorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France. gilles.fischer@sorbonne-universite.fr.ORCID http://orcid.org/0000-0001-5732-2682
Stéphane Delmas *Sorbonne Université, CNRS, Computational, Quantitative and Synthetic Biology, CQSB, F-75005, Paris, France. stephane.delmas@sorbonne-universite.fr.ORCID http://orcid.org/0000-0001-5523-7548

Funding

Agence Nationale de la Recherche (ANR) 16-CE12-0019Agence Nationale de la Recherche (ANR) 18-CE12-0004Agence Nationale de la Recherche (ANR) 20-CE12-0020Agence Nationale de la Recherche (ANR) 24-CE12-0998
6 · The paper itself

Abstract

Characterizing the contribution of mutators to mutation accumulation is essential for understanding cellular adaptation and diseases like cancer. By measuring single and double mutation rates, including point mutations, segmental duplications, and reciprocal translocations, we found that wild-type yeast colonies exhibit double mutation rates up to 17 times higher than expected from experimentally determined single mutation rates. These double mutants retained wild-type mutation rates, indicating they originated from genetically normal cells that transiently expressed a mutator phenotype. Numerical simulations suggest that transient mutator subpopulations likely consist of less than a few thousand cells, and experience high-intensity mutational bursts for less than five generations. Most double mutations accumulated sequentially across cell cycles, with simultaneous acquisition being rare and likely linked to systemic genomic instability. Additionally, we explored the genetic control of transient hypermutation and found that the excess of double mutants can be modulated by replication stress and the DNA damage tolerance pathway. Our findings suggest that transient mutators play a significant role in genomic instability and contribute to the mutational load accumulating in growing isogenic populations.

Indexed as

MutationSaccharomyces cerevisiaeDNA DamageDNA ReplicationGenomic InstabilityMutation AccumulationMutation RateGenome InstabilityMutation RatesSaccharomyces cerevisiaeTransient MutatorYeast

Identifiers

PMID40490499
PMCPMC12405527

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.