Evidence map›Paper›PMID 40571846›Full record

ArticleMolecular systems biology2025

Compensatory evolution to DNA replication stress is robust to nutrient availability.

Mariana Natalino, Marco Fumasoni

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. Experimental evolution of cellular miniaturization reveals a putative mechanism for cell size evolution.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Mariana NatalinoGulbenkian Institute for Molecular Medicine (GIMM), Lisbon, Portugal.ORCID http://orcid.org/0000-0003-4757-8232
Marco FumasoniGulbenkian Institute for Molecular Medicine (GIMM), Lisbon, Portugal. marco.fumasoni@gimm.pt.ORCID http://orcid.org/0000-0002-4507-7824

Funding

EC | Horizon Europe | Excellent Science | HORIZON EUROPE Marie Sklodowska-Curie Actions (MSCA) 101030203European Molecular Biology Organization (EMBO) 5349-2023Fundação Calouste Gulbenkian (Calouste Gulbenkian Foundation) GMEHuman Frontier Science Program (HFSP) RGEC28/2023MEC | Fundação para a Ciência e a Tecnologia (FCT) 2022.07846.PTDCMEC | Fundação para a Ciência e a Tecnologia (FCT) 2023.09068.CEECINDMEC | Fundação para a Ciência e a Tecnologia (FCT) UI/BD/152252/2021
6 · The paper itself

Abstract

Evolutionary repair refers to the compensatory evolution that follows perturbations in cellular processes. While evolutionary trajectories are often reproducible, other studies suggest they are shaped by genotype-by-environment (GxE) interactions. Here, we test the predictability of evolutionary repair in response to DNA replication stress-a severe perturbation impairing the conserved mechanisms of DNA synthesis, resulting in genetic instability. We conducted high-throughput experimental evolution on Saccharomyces cerevisiae experiencing constitutive replication stress, grown under different glucose availability. We found that glucose levels impact the physiology and adaptation rate of replication stress mutants. However, the genetics of adaptation show remarkable robustness across environments. Recurrent mutations collectively recapitulated the fitness of evolved lines and are advantageous across macronutrient availability. We also identified a novel role of the mediator complex of RNA polymerase II in adaptation to replicative stress. Our results highlight the robustness and predictability of evolutionary repair mechanisms to DNA replication stress and provide new insights into the evolutionary aspects of genome stability, with potential implications for understanding cancer development.

Indexed as

DNA ReplicationEvolution, MolecularSaccharomyces cerevisiaeStress, PhysiologicalAdaptation, PhysiologicalDNA RepairGenomic InstabilityGlucoseMutationNutrientsSaccharomyces cerevisiae ProteinsGlucoseNutrientsSaccharomyces cerevisiae ProteinsCompensatory EvolutionDNA Replication StressGenome MaintenanceNutrientsS. cerevisiae

Identifiers

PMID40571846
PMCPMC12494895

What OpenQuestion holds

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Registered trials

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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.