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DNA polymerase ε and δ proofreading suppress discrete mutator and cancer phenotypes in mice

https://doi.org/10.1073/pnas.0907147106
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/humu.20047openalex-snapshot
Structural and functional analysis of mutations at the human hypoxanthine phosphoribosyl transferase (HPRT1) locus
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07751.xopenalex-snapshot
The 3′ to 5′ exonuclease activity located in the DNA polymerase delta subunit of Saccharomyces cerevisiae is required for accurate replication.
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05790.xopenalex-snapshot
Pathway correcting DNA replication errors in Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1006/jmbi.2000.3744openalex-snapshot
Evidence from mutational specificity studies that yeast DNA polymerases δ and ϵ replicate different DNA strands at an intracellular replication fork 1 1Edited by A. R. Fersht
inferredcites →https://doi.org/10.1007/bf00280418openalex-snapshot
The 3′ → 5′ exonucleases of both DNA polymerases δ and ε participate in correcting errors of DNA replication in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0092-8674(89)90883-0openalex-snapshot
A conserved 3′→5′ exonuclease active site in prokaryotic and eukaryotic DNA polymerases
inferredcites →https://doi.org/10.1016/j.molcel.2008.02.022openalex-snapshot
Division of Labor at the Eukaryotic Replication Fork
inferredcites →https://doi.org/10.1016/j.tcb.2008.08.005openalex-snapshot
Dividing the workload at a eukaryotic replication fork
inferredcites →https://doi.org/10.1016/s0027-5107(97)00248-0openalex-snapshot
Comparison between in vivo mutagenicity and carcinogenicity in multiple organs by benzo[a]pyrene in the lacZ transgenic mouse (Muta™Mouse)
inferredcites →https://doi.org/10.1016/s0027-5107(98)00032-3openalex-snapshot
No direct correlation between mutant frequencies and cancer incidence induced by MeIQ in various organs of Big Blue® mice
inferredcites →https://doi.org/10.1016/s0074-7696(06)55002-8openalex-snapshot
Roles of DNA Polymerases in Replication, Repair, and Recombination in Eukaryotes
inferredcites →https://doi.org/10.1016/s0079-6603(08)00004-4openalex-snapshot
DNA Polymerase ε: A Polymerase of Unusual Size (and Complexity)
inferredcites →https://doi.org/10.1016/s1471-4914(02)02359-6openalex-snapshot
Mouse models for human DNA mismatch-repair gene defects
inferredcites →https://doi.org/10.1021/cr0404794openalex-snapshot
DNA Mismatch Repair: Functions and Mechanisms
inferredcites →https://doi.org/10.1038/362709a0openalex-snapshot
Instability and decay of the primary structure of DNA
inferredcites →https://doi.org/10.1038/88963openalex-snapshot
Defective DNA polymerase-δ proofreading causes cancer susceptibility in mice
inferredcites →https://doi.org/10.1038/cr.2008.4openalex-snapshot
The fidelity of DNA synthesis by eukaryotic replicative and translesion synthesis polymerases
inferredcites →https://doi.org/10.1038/nrm804openalex-snapshot
The 3′–5′ exonucleases
inferredcites →https://doi.org/10.1042/0264-6021:3560685openalex-snapshot
Structural similarities of Na,K-ATPase and SERCA, the Ca2+-ATPase of the sarcoplasmic reticulum
inferredcites →https://doi.org/10.1073/pnas.0607057103openalex-snapshot
Human cancers express a mutator phenotype
inferredcites →https://doi.org/10.1073/pnas.232340999openalex-snapshot
High incidence of epithelial cancers in mice deficient for DNA polymerase δ proofreading
inferredcites →https://doi.org/10.1073/pnas.88.21.9473openalex-snapshot
Eukaryotic DNA polymerase amino acid sequence required for 3'----5' exonuclease activity.
inferredcites →https://doi.org/10.1073/pnas.93.17.9073openalex-snapshot
Analysis of genetic instability during mammary tumor progression using a novel selection-based assay for in vivo mutations in a bacteriophage lambda transgene target.
inferredcites →https://doi.org/10.1073/pnas.94.7.3122openalex-snapshot
Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2
inferredcites →https://doi.org/10.1074/jbc.m110615200openalex-snapshot
Human DNA Polymerase ε Colocalizes with Proliferating Cell Nuclear Antigen and DNA Replication Late, but Not Early, in S Phase
inferredcites →https://doi.org/10.1080/10409230590935433openalex-snapshot
DNA Polymerases that Propagate the Eukaryotic DNA Replication Fork
inferredcites →https://doi.org/10.1093/carcin/bgl079openalex-snapshot
Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6
inferredcites →https://doi.org/10.1093/genetics/142.3.717openalex-snapshot
3′ → 5′ Exonucleases of DNA Polymerases ϵ and δ Correct Base Analog Induced DNA Replication Errors on Opposite DNA Strands in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/genetics/148.4.1667openalex-snapshot
Rates of Spontaneous Mutation
inferredcites →https://doi.org/10.1111/j.1742-4658.2006.05310.xopenalex-snapshot
Distinctive activities of DNA polymerases during human DNA replication
inferredcites →https://doi.org/10.1126/science.1144067openalex-snapshot
Yeast DNA Polymerase ε Participates in Leading-Strand DNA Replication
inferredcites →https://doi.org/10.1128/9781555816704openalex-snapshot
DNA Repair and Mutagenesis
inferredcites →https://doi.org/10.1128/mcb.19.3.2000openalex-snapshot
The 3′→5′ Exonucleases of DNA Polymerases δ and ɛ and the 5′→3′ Exonuclease Exo1 Have Major Roles in Postreplication Mutation Avoidance in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1146/annurev.biochem.73.011303.073859openalex-snapshot
CELLULAR DNA REPLICASES: Components and Dynamics at the Replication Fork

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Race, Prevalence of POLE and POLD1 Alterations, and Survival Among Patients With Endometrial Cancer
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Evaluation of POLE/POLD1 Variants as Potential Biomarkers for Immune Checkpoint Inhibitor Treatment Outcomes
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p12 isoform‐2 is a regulatory subunit of human DNA polymerase delta and is dysregulated in various cancers
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POLE somatic mutations in advanced colorectal cancer
inferred← citeshttps://doi.org/10.1002/cam4.305openalex-snapshot
Mutations in POLE and survival of colorectal cancer patients – link to disease stage and treatment
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Polymerase ɛ ( POLE ) mutations in endometrial cancer: Clinical outcomes and implications for L ynch syndrome testing
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POLE mutations as an alternative pathway for microsatellite instability in endometrial cancer: Implications for L ynch syndrome testing
inferred← citeshttps://doi.org/10.1002/em.21731openalex-snapshot
Mouse models of DNA polymerases
inferred← citeshttps://doi.org/10.1002/em.21735openalex-snapshot
Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools
inferred← citeshttps://doi.org/10.1002/em.21745openalex-snapshot
DNA polymerase delta in dna replication and genome maintenance
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DNA polymerase ε and its roles in genome stability
inferred← citeshttps://doi.org/10.1002/path.4185openalex-snapshot
Germline and somatic polymerase ϵ and δ mutations define a new class of hypermutated colorectal and endometrial cancers
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Future Directions and New Targets in Endometrial Cancer
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Eukaryotic Replicative DNA Polymerases
inferred← citeshttps://doi.org/10.1007/978-3-642-39796-7_3openalex-snapshot
DNA Repair Polymerases
inferred← citeshttps://doi.org/10.1007/978-94-007-4572-8_12openalex-snapshot
Structure and Function of Eukaryotic DNA Polymerase δ
inferred← citeshttps://doi.org/10.1007/978-981-15-1067-0_6openalex-snapshot
Genomic Instability and Cancer Metastasis
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Site directed mutagenesis reveals functional importance of conserved amino acid residues within the N-terminal domain of Dpb2 in budding yeast
inferred← citeshttps://doi.org/10.1007/s00285-024-02134-4openalex-snapshot
Error-induced extinction in a multi-type critical birth–death process
inferred← citeshttps://doi.org/10.1007/s00294-018-0820-1openalex-snapshot
Fidelity of DNA replication—a matter of proofreading
inferred← citeshttps://doi.org/10.1007/s10555-013-9426-8openalex-snapshot
Do mutator mutations fuel tumorigenesis?
inferred← citeshttps://doi.org/10.1007/s10689-015-9803-2openalex-snapshot
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine
inferred← citeshttps://doi.org/10.1007/s10689-015-9826-8openalex-snapshot
POLE mutations in families predisposed to cutaneous melanoma
inferred← citeshttps://doi.org/10.1007/s11357-024-01113-3openalex-snapshot
Somatic mutations in aging and disease
inferred← citeshttps://doi.org/10.1007/s12029-023-00927-2openalex-snapshot
Immune Checkpoint Inhibitors in pMMR/MSS Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/s12672-025-03652-3openalex-snapshot
Endometrial cancer: from clinical reality to molecular treatment
inferred← citeshttps://doi.org/10.1016/b978-0-12-397933-9.00025-4openalex-snapshot
Immune Deficiencies Caused by B Cell Defects
inferred← citeshttps://doi.org/10.1016/b978-0-12-803309-8.00017-3openalex-snapshot
Base Excision Repair and Nucleotide Excision Repair
inferred← citeshttps://doi.org/10.1016/b978-0-323-85679-9.00017-9openalex-snapshot
Base excision repair and nucleotide excision repair
inferred← citeshttps://doi.org/10.1016/bs.acr.2021.03.003openalex-snapshot
Unraveling the genomic landscape of colorectal cancer through mutational signatures
inferred← citeshttps://doi.org/10.1016/j.annonc.2024.03.009openalex-snapshot
Immune checkpoint inhibitors for POLE or POLD1 proofreading-deficient metastatic colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.arr.2024.102268openalex-snapshot
Somatic mutations in human ageing: New insights from DNA sequencing and inherited mutations
inferred← citeshttps://doi.org/10.1016/j.cbpa.2011.07.025openalex-snapshot
Balancing eukaryotic replication asymmetry with replication fidelity
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Comprehensive Analysis of Hypermutation in Human Cancer
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Early onset sporadic colorectal cancer: Worrisome trends and oncogenic features
inferred← citeshttps://doi.org/10.1016/j.dnarep.2011.02.003openalex-snapshot
The in vitro fidelity of yeast DNA polymerase δ and polymerase ɛ holoenzymes during dinucleotide microsatellite DNA synthesis
inferred← citeshttps://doi.org/10.1016/j.dnarep.2013.08.012openalex-snapshot
Human Pol ɛ-dependent replication errors and the influence of mismatch repair on their correction
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.04.006openalex-snapshot
Quantifying the contributions of base selectivity, proofreading and mismatch repair to nuclear DNA replication in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.11.020openalex-snapshot
Non-canonical actions of mismatch repair
inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.06.003openalex-snapshot
Replicative DNA polymerase defects in human cancers: Consequences, mechanisms, and implications for therapy
inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.11.005openalex-snapshot
DNA Replication and associated repair pathways are involved in the mutagenesis of methylated cytosine
inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.02.007openalex-snapshot
POLE proofreading defects: Contributions to mutagenesis and cancer
inferred← citeshttps://doi.org/10.1016/j.dnarep.2024.103694openalex-snapshot
The mutagenic consequences of defective DNA repair
inferred← citeshttps://doi.org/10.1016/j.dnarep.2025.103885openalex-snapshot
Proofreading exonuclease activities of Polδ and Polε differentially contribute to the removal of chain-terminating nucleoside analogs
inferred← citeshttps://doi.org/10.1016/j.gde.2013.12.005openalex-snapshot
Replicative DNA polymerase mutations in cancer
inferred← citeshttps://doi.org/10.1016/j.gene.2016.06.031openalex-snapshot
POLD1: Central mediator of DNA replication and repair, and implication in cancer and other pathologies
inferred← citeshttps://doi.org/10.1016/j.gore.2015.01.005openalex-snapshot
Improved survival of patients with hypermutation in uterine serous carcinoma
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e28044openalex-snapshot
Single base substitution signatures 17a, 17b, and 40 are induced by γ-ray irradiation in association with increased reactive oxidative species
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104705openalex-snapshot
Genome-wide contributions of the MutSα- and MutSβ-dependent DNA mismatch repair pathways to the maintenance of genetic stability in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.jmoldx.2025.12.004openalex-snapshot
Phenotypic POLE Variant Classification Identifies Patients Who May Have Favorable Prognosis and Benefit from Immunotherapy
inferred← citeshttps://doi.org/10.1016/j.mad.2011.10.009openalex-snapshot
Somatic mutations in aging, cancer and neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.matbio.2013.05.001openalex-snapshot
Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.05.003openalex-snapshot
DNA Replication—A Matter of Fidelity
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.05.012openalex-snapshot
POLE Mutation Spectra Are Shaped by the Mutant Allele Identity, Its Abundance, and Mismatch Repair Status
inferred← citeshttps://doi.org/10.1016/j.molmed.2023.04.002openalex-snapshot
Mitigating age-related somatic mutation burden
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.07.003openalex-snapshot
Aberrant DNA replication in cancer
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2014.01.003openalex-snapshot
Frequent POLE1 p.S297F mutation in Chinese patients with ovarian endometrioid carcinoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2010.10.001openalex-snapshot
Aberrant expression of alternative DNA polymerases: A source of mutator phenotype as well as replicative stress in cancer
inferred← citeshttps://doi.org/10.1016/j.semcancer.2010.10.009openalex-snapshot
DNA replication fidelity and cancer
inferred← citeshttps://doi.org/10.1016/j.semcancer.2015.03.005openalex-snapshot
Genomic instability in human cancer: Molecular insights and opportunities for therapeutic attack and prevention through diet and nutrition
inferred← citeshttps://doi.org/10.1016/j.semdp.2026.151033openalex-snapshot
The current molecular landscape of endometrial and ovarian carcinomas: insights and practical updates
inferred← citeshttps://doi.org/10.1016/j.tig.2020.12.003openalex-snapshot
Underappreciated Roles of DNA Polymerase δ in Replication Stress Survival
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.02.020openalex-snapshot
Differential genomic destabilisation in human cells with pathogenic MSH2 mutations introduced by genome editing
inferred← citeshttps://doi.org/10.1016/j.ygyno.2015.04.027openalex-snapshot
Polymerase ε (POLE) ultra-mutated tumors induce robust tumor-specific CD4+ T cell responses in endometrial cancer patients
inferred← citeshttps://doi.org/10.1016/j.ygyno.2016.11.023openalex-snapshot
Polymerase ε (POLE) ultra-mutation in uterine tumors correlates with T lymphocyte infiltration and increased resistance to platinum-based chemotherapy in vitro
inferred← citeshttps://doi.org/10.1016/j.ygyno.2016.12.015openalex-snapshot
Molecular approaches for classifying endometrial carcinoma
inferred← citeshttps://doi.org/10.1016/j.yrtph.2015.12.018openalex-snapshot
HESI/FDA workshop on immunomodulators and cancer risk assessment: Building blocks for a weight-of-evidence approach
inferred← citeshttps://doi.org/10.1038/ejhg.2010.216openalex-snapshot
Concurrent genetic alterations in DNA polymerase proofreading and mismatch repair in human colorectal cancer
inferred← citeshttps://doi.org/10.1038/gim.2015.75openalex-snapshot
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance
inferred← citeshttps://doi.org/10.1038/ncomms5990openalex-snapshot
Phenotypic characterization of missense polymerase-δ mutations using an inducible protein-replacement system
inferred← citeshttps://doi.org/10.1038/ng.2503openalex-snapshot
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
inferred← citeshttps://doi.org/10.1038/ng.2540openalex-snapshot
The burden of faulty proofreading in colon cancer
inferred← citeshttps://doi.org/10.1038/nmeth.1781openalex-snapshot
Decoding cell lineage from acquired mutations using arbitrary deep sequencing
inferred← citeshttps://doi.org/10.1038/nrc.2015.12openalex-snapshot
A panoply of errors: polymerase proofreading domain mutations in cancer
inferred← citeshttps://doi.org/10.1038/nrc2998openalex-snapshot
DNA polymerases and cancer
inferred← citeshttps://doi.org/10.1038/nrc3063openalex-snapshot
Human cancers express mutator phenotypes: origin, consequences and targeting
inferred← citeshttps://doi.org/10.1038/nsmb.2852openalex-snapshot
Delivering nonidentical twins
inferred← citeshttps://doi.org/10.1038/onc.2013.339openalex-snapshot
Role of DNA damage response pathways in preventing carcinogenesis caused by intrinsic replication stress
inferred← citeshttps://doi.org/10.1038/s10038-019-0611-7openalex-snapshot
Development of an MSI-positive colon tumor with aberrant DNA methylation in a PPAP patient
inferred← citeshttps://doi.org/10.1038/s41431-024-01598-8openalex-snapshot
Discovery of recessive effect of human polymerase δ proofreading deficiency through mutational analysis of POLD1-mutated normal and cancer cells
inferred← citeshttps://doi.org/10.1038/s41467-018-04002-4openalex-snapshot
Distinct mutational signatures characterize concurrent loss of polymerase proofreading and mismatch repair
inferred← citeshttps://doi.org/10.1038/s41467-018-08114-9openalex-snapshot
Structural consequence of the most frequently recurring cancer-associated substitution in DNA polymerase ε
inferred← citeshttps://doi.org/10.1038/s41568-024-00705-7openalex-snapshot
Defining clinically useful biomarkers of immune checkpoint inhibitors in solid tumours
inferred← citeshttps://doi.org/10.1038/s41568-026-00958-4openalex-snapshot
The DNA damage response and cancer immunotherapy
inferred← citeshttps://doi.org/10.1038/s41573-025-01212-6openalex-snapshot
Targeting DNA damage in ageing: towards supercharging DNA repair
inferred← citeshttps://doi.org/10.1038/s41588-021-00930-yopenalex-snapshot
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
inferred← citeshttps://doi.org/10.1038/s41588-022-01108-wopenalex-snapshot
Functional landscapes of POLE and POLD1 mutations in checkpoint blockade-dependent antitumor immunity
inferred← citeshttps://doi.org/10.1038/s41588-024-01945-xopenalex-snapshot
Human DNA polymerase ε is a source of C>T mutations at CpG dinucleotides
inferred← citeshttps://doi.org/10.1038/s41594-021-00691-6openalex-snapshot
How asymmetric DNA replication achieves symmetrical fidelity
inferred← citeshttps://doi.org/10.1038/srep36971openalex-snapshot
Mutation tendency of mutator Plasmodium berghei with proofreading-deficient DNA polymerase δ
inferred← citeshttps://doi.org/10.1038/srep46535openalex-snapshot
Normally lethal amino acid substitutions suppress an ultramutator DNA Polymerase δ variant
inferred← citeshttps://doi.org/10.1073/pnas.0914857107openalex-snapshot
Abundant ribonucleotide incorporation into DNA by yeast replicative polymerases
inferred← citeshttps://doi.org/10.1073/pnas.1013048107openalex-snapshot
Differential correction of lagging-strand replication errors made by DNA polymerases α and δ
inferred← citeshttps://doi.org/10.1073/pnas.1217425110openalex-snapshot
Dual role for mammalian DNA polymerase ζ in maintaining genome stability and proliferative responses
inferred← citeshttps://doi.org/10.1073/pnas.1422934112openalex-snapshot
Colon cancer-associated mutator DNA polymerase δ variant causes expansion of dNTP pools increasing its own infidelity
inferred← citeshttps://doi.org/10.1073/pnas.1422948112openalex-snapshot
dNTP pool levels modulate mutator phenotypes of error-prone DNA polymerase ε variants
inferred← citeshttps://doi.org/10.1073/pnas.1507165112openalex-snapshot
Formation of interference-sensitive meiotic cross-overs requires sufficient DNA leading-strand elongation
inferred← citeshttps://doi.org/10.1073/pnas.1917624117openalex-snapshot
DNA polymerase δ proofreads errors made by DNA polymerase ε
inferred← citeshttps://doi.org/10.1073/pnas.2526551123openalex-snapshot
Polymerase ι promotes C>T substitutions in smoking models and in the platinum chemotherapy–induced SBS31 mutation signature
inferred← citeshttps://doi.org/10.1074/jbc.m110.147017openalex-snapshot
Active Site Mutations in Mammalian DNA Polymerase δ Alter Accuracy and Replication Fork Progression
inferred← citeshttps://doi.org/10.1074/jbc.m112.422733openalex-snapshot
Human DNA Polymerase ϵ Is Able to Efficiently Extend from Multiple Consecutive Ribonucleotides
inferred← citeshttps://doi.org/10.1074/jbc.m114.615278openalex-snapshot
Yeast DNA Polymerase ϵ Catalytic Core and Holoenzyme Have Comparable Catalytic Rates
inferred← citeshttps://doi.org/10.1074/jbc.ra118.003477openalex-snapshot
Impact of tobacco-specific nitrosamine–derived DNA adducts on the efficiency and fidelity of DNA replication in human cells
inferred← citeshttps://doi.org/10.1080/07853890.2025.2583543openalex-snapshot
TCGA molecular subtypes in endometriosis-associated ovarian cancer: a systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1080/10409238.2020.1811630openalex-snapshot
An updated perspective on the polymerase division of labor during eukaryotic DNA replication
inferred← citeshttps://doi.org/10.1080/15384101.2017.1404208openalex-snapshot
DNA polymerase η mutational signatures are found in a variety of different types of cancer
inferred← citeshttps://doi.org/10.1080/19491034.2016.1205774openalex-snapshot
Reconstitution of a eukaryotic replisome reveals the mechanism of asymmetric distribution of DNA polymerases
inferred← citeshttps://doi.org/10.1084/jem.20121303openalex-snapshot
Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature (“FILS syndrome”)
inferred← citeshttps://doi.org/10.1089/crispr.2019.0006openalex-snapshot
CRISPR-Cas9 Causes Chromosomal Instability and Rearrangements in Cancer Cell Lines, Detectable by Cytogenetic Methods
inferred← citeshttps://doi.org/10.1093/database/baaf076openalex-snapshot
PolED: a manually curated database of functional studies of POLE and POLD1 variants reported in humans
inferred← citeshttps://doi.org/10.1093/femsre/fuaa038openalex-snapshot
DNA damage bypass pathways and their effect on mutagenesis in yeast
inferred← citeshttps://doi.org/10.1093/hmg/ddq175openalex-snapshot
The nucleotide composition of microsatellites impacts both replication fidelity and mismatch repair in human colorectal cells
inferred← citeshttps://doi.org/10.1093/hmg/ddt131openalex-snapshot
DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer
inferred← citeshttps://doi.org/10.1093/mutage/gez049openalex-snapshot
The double-edged sword of cancer mutations: exploiting neoepitopes for the fight against cancer
inferred← citeshttps://doi.org/10.1093/nar/gkaa633openalex-snapshot
Mismatch repair and DNA polymerase δ proofreading prevent catastrophic accumulation of leading strand errors in cells expressing a cancer-associated DNA polymerase ϵ variant
inferred← citeshttps://doi.org/10.1093/nar/gkac602openalex-snapshot
Enhanced polymerase activity permits efficient synthesis by cancer-associated DNA polymerase ϵ variants at low dNTP levels
inferred← citeshttps://doi.org/10.1093/nar/gkae843openalex-snapshot
Altered dNTP pools accelerate tumor formation in mice
inferred← citeshttps://doi.org/10.1093/nar/gkq1034openalex-snapshot
The high fidelity and unique error signature of human DNA polymerase
inferred← citeshttps://doi.org/10.1093/nar/gkr142openalex-snapshot
A random mutation capture assay to detect genomic point mutations in mouse tissue
inferred← citeshttps://doi.org/10.1093/nar/gkv1298openalex-snapshot
Genome-wide analysis of the specificity and mechanisms of replication infidelity driven by imbalanced dNTP pools
inferred← citeshttps://doi.org/10.1093/nar/gkx611openalex-snapshot
Human DNA polymerase delta double-mutant D316A;E318A interferes with DNA mismatch repair in vitro
inferred← citeshttps://doi.org/10.1093/nar/gkx625openalex-snapshot
Polμ tumor variants decrease the efficiency and accuracy of NHEJ
inferred← citeshttps://doi.org/10.1093/narcan/zcad011openalex-snapshot
The hereditary N363K POLE exonuclease mutant extends PPAP tumor spectrum to glioblastomas by causing DNA damage and aneuploidy in addition to increased mismatch mutagenicity
inferred← citeshttps://doi.org/10.1093/narcan/zcad033openalex-snapshot
Replication DNA polymerases, genome instability and cancer therapies
inferred← citeshttps://doi.org/10.1093/neuonc/nov027openalex-snapshot
Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis
inferred← citeshttps://doi.org/10.1097/igc.0000000000000492openalex-snapshot
Polymerase Epsilon Exonuclease Domain Mutations in Ovarian Endometrioid Carcinoma
inferred← citeshttps://doi.org/10.1097/igc.0000000000000681openalex-snapshot
Prognostic Significance of POLE Exonuclease Domain Mutations in High-Grade Endometrioid Endometrial Cancer on Survival and Recurrence
inferred← citeshttps://doi.org/10.1097/pas.0000000000000873openalex-snapshot
Undifferentiated and Dedifferentiated Endometrial Carcinomas With POLE Exonuclease Domain Mutations Have a Favorable Prognosis
inferred← citeshttps://doi.org/10.1101/2022.01.10.475213openalex-snapshot
A Simple Bypass Assay for DNA Polymerases Shows Hypermutating Variants Associated with Cancer Show Mechanistic Differences In Vitro
inferred← citeshttps://doi.org/10.1101/2022.07.20.500591openalex-snapshot
Extended family with an inherited pathogenic variant in polymerase delta provides strong evidence for recessive effect of proofreading deficiency in human cells
inferred← citeshttps://doi.org/10.1101/2024.06.10.597960openalex-snapshot
Immune Checkpoint Blockade Delays Cancer and Extends Survival in Murine DNA Polymerase Mutator Syndromes
inferred← citeshttps://doi.org/10.1101/2024.10.09.617451openalex-snapshot
DNA Polymerase Locks Replication Fork Under Stress
inferred← citeshttps://doi.org/10.1101/2025.04.07.646990openalex-snapshot
Exploring the mechanisms of early acquired resistance to doxorubicin in melanoma spheroids
inferred← citeshttps://doi.org/10.1101/2025.09.02.673565openalex-snapshot
Reductive evolution of the DNA replication machinery in endosymbiotic fungi
inferred← citeshttps://doi.org/10.1101/gad.349431.122openalex-snapshot
DNA repair defects in cancer and therapeutic opportunities
inferred← citeshttps://doi.org/10.1101/gr.178335.114openalex-snapshot
Heterogeneous polymerase fidelity and mismatch repair bias genome variation and composition
inferred← citeshttps://doi.org/10.1101/gr.186148.114openalex-snapshot
Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice
inferred← citeshttps://doi.org/10.1101/gr.226845.117openalex-snapshot
Mutational signatures of DNA mismatch repair deficiency in C. elegans and human cancers
inferred← citeshttps://doi.org/10.1101/gr.238543.118openalex-snapshot
Quantification of somatic mutation flow across individual cell division events by lineage sequencing
inferred← citeshttps://doi.org/10.1111/febs.16936openalex-snapshot
A simple bypass assay for DNA polymerases shows that cancer‐associated hypermutating variants exhibit differences in vitro
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2009.00393.xopenalex-snapshot
Phylogenetic analysis of developmental and postnatal mouse cell lineages
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2012.06590.xopenalex-snapshot
Implications of genetic heterogeneity in cancer
inferred← citeshttps://doi.org/10.1126/science.1191125openalex-snapshot
Increased Mutagenesis and Unique Mutation Signature Associated with Mitotic Gene Conversion
inferred← citeshttps://doi.org/10.1126/science.1211154openalex-snapshot
Aneuploidy Drives a Mutator Phenotype in Cancer
inferred← citeshttps://doi.org/10.1128/jvi.02028-21openalex-snapshot
BK Polyomavirus Requires the Mismatch Repair Pathway for DNA Damage Response Activation
inferred← citeshttps://doi.org/10.1128/spectrum.01210-25openalex-snapshot
Entamoeba histolytica “mutator” strain with a high rate of genetic mutations assists the elucidation of drug resistance mechanisms
inferred← citeshttps://doi.org/10.1134/s0006297922010023openalex-snapshot
Effect of DNA Methylation on the 3′→5′ Exonuclease Activity of Major Human Abasic Site Endonuclease APEX1
inferred← citeshttps://doi.org/10.1134/s1019331622040256openalex-snapshot
Mechanisms of Coronavirus Genome Stability As Potential Targets for Antiviral Drugs
inferred← citeshttps://doi.org/10.1136/jitc-2021-002336openalex-snapshot
Additive effects of variants of unknown significance in replication repair-associated DNA polymerase genes on mutational burden and prognosis across diverse cancers
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100616-060447openalex-snapshot
The Inherent Asymmetry of DNA Replication
inferred← citeshttps://doi.org/10.1158/0008-5472.can-10-0784openalex-snapshot
Regulation of DNA Polymerase POLD4 Influences Genomic Instability in Lung Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-12-3342openalex-snapshot
The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology
inferred← citeshttps://doi.org/10.1158/0008-5472.can-13-2892openalex-snapshot
A Common Cancer-Associated DNA Polymerase ϵ Mutation Causes an Exceptionally Strong Mutator Phenotype, Indicating Fidelity Defects Distinct from Loss of Proofreading
inferred← citeshttps://doi.org/10.1158/0008-5472.can-14-0013openalex-snapshot
Colorectal Cancer Cell Lines Are Representative Models of the Main Molecular Subtypes of Primary Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-0624openalex-snapshot
Cancers from Novel Pole -Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-3241openalex-snapshot
Dissecting the Functional Significance of DNA Polymerase Mutations in Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-24-2589openalex-snapshot
Immune Checkpoint Blockade Delays Cancer Development and Extends Survival in DNA Polymerase Mutator Syndromes
inferred← citeshttps://doi.org/10.1158/0008-5472.can-25-3977openalex-snapshot
Deficiency in POLE Exonuclease Causes Synthetic Lethality in Highly Aneuploid Cancer Cells
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-15-0057openalex-snapshot
POLE Proofreading Mutations Elicit an Antitumor Immune Response in Endometrial Cancer
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-15-2233openalex-snapshot
Endometrial Carcinomas with POLE Exonuclease Domain Mutations Have a Favorable Prognosis
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-15-0399openalex-snapshot
miR-155 Overexpression Promotes Genomic Instability by Reducing High-fidelity Polymerase Delta Expression and Activating Error-Prone DSB Repair
inferred← citeshttps://doi.org/10.1158/2159-8290.cd-16-0146openalex-snapshot
Personalized Oncology Meets Immunology: The Path toward Precision Immunotherapy
inferred← citeshttps://doi.org/10.1159/000455753openalex-snapshot
Fragile Genes That Are Frequently Altered in Cancer: Players Not Passengers
inferred← citeshttps://doi.org/10.1172/jci122095openalex-snapshot
Polymerase-mediated ultramutagenesis in mice produces diverse cancers with high mutational load
inferred← citeshttps://doi.org/10.1177/0192623310362249openalex-snapshot
Case Series
inferred← citeshttps://doi.org/10.1186/1471-2164-14-39openalex-snapshot
Use of somatic mutations to quantify random contributions to mouse development
inferred← citeshttps://doi.org/10.1186/s12864-023-09310-8openalex-snapshot
Candidate variants in DNA replication and repair genes in early-onset renal cell carcinoma patients referred for germline testing
inferred← citeshttps://doi.org/10.1186/s12885-016-2544-2openalex-snapshot
Changes in mitochondrial stability during the progression of the Barrett’s esophagus disease sequence
inferred← citeshttps://doi.org/10.1186/s12916-025-04611-zopenalex-snapshot
The clinical landscape of POLE-mutant colorectal cancer: a retrospective analysis of real-world outcome
inferred← citeshttps://doi.org/10.1186/s13046-022-02422-1openalex-snapshot
POLE/POLD1 mutation and tumor immunotherapy
inferred← citeshttps://doi.org/10.1186/s13073-023-01234-yopenalex-snapshot
Recommendations for the classification of germline variants in the exonuclease domain of POLE and POLD1
inferred← citeshttps://doi.org/10.1200/po-25-00382openalex-snapshot
Secondary POLE Mutation Drives Metastasis in Hereditary Breast and Ovarian Cancer: Revealing Fallopian Tube Ultramutation
inferred← citeshttps://doi.org/10.1200/po.21.00267openalex-snapshot
Clinical and Molecular Characterization of POLE Mutations as Predictive Biomarkers of Response to Immune Checkpoint Inhibitors in Advanced Cancers
inferred← citeshttps://doi.org/10.1201/b14587-4openalex-snapshot
Genetic Instability of Cancer
inferred← citeshttps://doi.org/10.1266/ggs.18-00015openalex-snapshot
Spontaneous de novo germline mutations in humans and mice: rates, spectra, causes and consequences
inferred← citeshttps://doi.org/10.1371/annotation/db1d9553-4ebd-4015-a1cd-c483dbc0d7e5openalex-snapshot
Correction: Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast
inferred← citeshttps://doi.org/10.1371/journal.pgen.1001209openalex-snapshot
Mismatch Repair–Independent Increase in Spontaneous Mutagenesis in Yeast Lacking Non-Essential Subunits of DNA Polymerase ε
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002282openalex-snapshot
Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002680openalex-snapshot
Recombination Drives Vertebrate Genome Contraction
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003016openalex-snapshot
Mismatch Repair Balances Leading and Lagging Strand DNA Replication Fidelity
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003899openalex-snapshot
A Reversible Histone H3 Acetylation Cooperates with Mismatch Repair and Replicative Polymerases in Maintaining Genome Stability
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005049openalex-snapshot
Replicative DNA Polymerase δ but Not ε Proofreads Errors in Cis and in Trans
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005151openalex-snapshot
Volatility of Mutator Phenotypes at Single Cell Resolution
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009526openalex-snapshot
Expression of the cancer-associated DNA polymerase ε P286R in fission yeast leads to translesion synthesis polymerase dependent hypermutation and defective DNA replication
inferred← citeshttps://doi.org/10.1515/bjmg-2017-0028openalex-snapshot
Detection of allelic variants of the POLE and POLD1 genes in colorectal cancer patients
inferred← citeshttps://doi.org/10.15252/embj.2019103367openalex-snapshot
Excessive excision of correct nucleotides during DNA synthesis explained by replication hurdles
inferred← citeshttps://doi.org/10.1530/ec-20-0258openalex-snapshot
POLE and POLD1 pathogenic variants in the proofreading domain in papillary thyroid cancer
inferred← citeshttps://doi.org/10.1534/g3.118.200042openalex-snapshot
Functional Analysis of Cancer-Associated DNA Polymerase ε Variants inSaccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1534/genetics.112.146910openalex-snapshot
Emergence of DNA Polymerase ε Antimutators That Escape Error-Induced Extinction in Yeast
inferred← citeshttps://doi.org/10.1534/genetics.113.160960openalex-snapshot
DNA Replication Error-Induced Extinction of Diploid Yeast
inferred← citeshttps://doi.org/10.1534/genetics.120.303333openalex-snapshot
Spontaneous Polyploids and Antimutators Compete During the Evolution of Saccharomyces cerevisiae Mutator Cells
inferred← citeshttps://doi.org/10.1534/genetics.120.303813openalex-snapshot
John W. (Jan) Drake: A Biochemical View of a Geneticist Par Excellence
inferred← citeshttps://doi.org/10.18632/oncotarget.16508openalex-snapshot
The dominant role of proofreading exonuclease activity of replicative polymerase ε in cellular tolerance to cytarabine (Ara-C)
inferred← citeshttps://doi.org/10.21037/atm-20-7553openalex-snapshot
Distinctive genomic characteristics in POLE/POLD1-mutant cancers can potentially predict beneficial clinical outcomes in patients who receive immune checkpoint inhibitor
inferred← citeshttps://doi.org/10.2174/1389200216666150812123554openalex-snapshot
Diallyl Sulfide: Potential Use in Novel Therapeutic Interventions in Alcohol, Drugs, and Disease Mediated Cellular Toxicity by Targeting Cytochrome P450 2E1
inferred← citeshttps://doi.org/10.2174/9789815080384123010007openalex-snapshot
Biology of Cancer
inferred← citeshttps://doi.org/10.26508/lsa.201900321openalex-snapshot
Human DNA polymerase delta requires an iron–sulfur cluster for high-fidelity DNA synthesis
inferred← citeshttps://doi.org/10.26508/lsa.201900323openalex-snapshot
Human DNA polymerase delta is a pentameric holoenzyme with a dimeric p12 subunit
inferred← citeshttps://doi.org/10.3103/s0027134920050124openalex-snapshot
Self-Organized Criticality in the Autowave Model of Speciation
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