Evidence map›Paper›PMID 41051315›Full record

ArticleMolecular biology and evolution2025

Comprehensive Mutational Landscape of Yeast Mutator Strains Reveals the Genetic Basis of Mutational Signatures in Cancer.

Lei Liu, Danyang Sun, Haoxuan Liu

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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  3. Review
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

3 authors.

Lei LiuCenter for Evolutionary & Organismal Biology and the Fourth Affiliated Hospital of Zhejiang University, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou 310058, People's Republic of China.ORCID 0009-0008-5439-550X
Danyang SunCenter for Evolutionary & Organismal Biology and the Fourth Affiliated Hospital of Zhejiang University, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou 310058, People's Republic of China.ORCID 0009-0004-8551-2546
Haoxuan LiuCenter for Evolutionary & Organismal Biology and the Fourth Affiliated Hospital of Zhejiang University, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou 310058, People's Republic of China.ORCID 0009-0009-1075-8185

Funding

National Key Research and Development Program of China 2024YFA1802500National Natural Science Foundation of China 32470646
6 · The paper itself

Abstract

Spontaneous mutation rates and spectra are influenced by an intricate interplay of processes including DNA replication, proofreading, and diverse DNA damage repair pathways. Although significant progress has been made in characterizing the functions of individual genes involved in these processes, their direct effects on mutation rates and spectra remain unclear. In this study, we employed a systematic gene knockout approach coupled with mutation accumulation (MA) experiments and whole-genome sequencing (WGS) to investigate the mutational landscape of Saccharomyces cerevisiae. We targeted 136 gene-deletion strains encompassing nearly all known genes associated with DNA replication and repair. Analysis of 1,081 MA lines revealed that 114 of the 136 genes significantly influenced at least one type of mutation rate. Furthermore, deletions of specific genes led to marked shifts in mutational biases and spectra, with some deletions amplifying existing biases and others reversing them entirely. In contrast, mitochondrial mutation rates were notably less affected, with no significant impact detected. Importantly, comparative analysis revealed striking similarities between yeast mutational spectrum and those observed in human cancers with the same pathway deficiencies, suggesting conserved functional roles across species. In conclusion, our findings provided critical insights into the genetic underpinnings of these signatures and underscoring the utility of yeast as a model for studying the molecular basis of cancer-associated mutational processes.

Indexed as

Mutation AccumulationMutation RateNeoplasmsSaccharomyces cerevisiaeDNA RepairDNA ReplicationGene DeletionGene Knockout TechniquesGenome, FungalGenomicsHumansWhole Genome Sequencinggene deletionmutation ratemutation signaturemutation spectrumyeast

Identifiers

PMID41051315
PMCPMC12559997

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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.