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Removal of Spo11 from meiotic DNA breaks in vitro but not in vivo by Tyrosyl DNA Phosphodiesterase 2
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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/j.1460-2075.1995.tb00138.xopenalex-snapshot
The nucleotide mapping of DNA double‐strand breaks at the CYS3 initiation site of meiotic recombination in Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00139.xopenalex-snapshot
The location and structure of double‐strand DNA breaks induced during yeast meiosis: evidence for a covalently linked DNA‐protein intermediate.
inferredcites →https://doi.org/10.1007/978-1-4939-0799-1_4openalex-snapshot
Yeast Transformation by the LiAc/SS Carrier DNA/PEG Method
inferredcites →https://doi.org/10.1007/978-1-4939-1363-3_1openalex-snapshot
Yeast Transformation by the LiAc/SS Carrier DNA/PEG Method
inferredcites →https://doi.org/10.1007/978-1-59745-527-5_12openalex-snapshot
End-Labeling and Analysis of Spo11-Oligonucleotide Complexes in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/0092-8674(90)90072-mopenalex-snapshot
A pathway for generation and processing of double-strand breaks during meiotic recombination in S. cerevisiae
inferredcites →https://doi.org/10.1016/j.cell.2011.02.009openalex-snapshot
A Hierarchical Combination of Factors Shapes the Genome-wide Topography of Yeast Meiotic Recombination Initiation
inferredcites →https://doi.org/10.1016/j.celrep.2014.11.044openalex-snapshot
Cdk1 Restrains NHEJ through Phosphorylation of XRCC4-like Factor Xlf1
inferredcites →https://doi.org/10.1016/j.dnarep.2010.11.008openalex-snapshot
Mre11 and Exo1 contribute to the initiation and processivity of resection at meiotic double-strand breaks made independently of Spo11
inferredcites →https://doi.org/10.1016/j.dnarep.2014.03.020openalex-snapshot
Tyrosyl-DNA-phosphodiesterases (TDP1 and TDP2)
inferredcites →https://doi.org/10.1016/j.molcel.2010.11.032openalex-snapshot
Temporally and Biochemically Distinct Activities of Exo1 during Meiosis: Double-Strand Break Resection and Resolution of Double Holliday Junctions
inferredcites →https://doi.org/10.1016/s0021-9258(19)41200-3openalex-snapshot
The specificity of lambda exonuclease. Interactions with single-stranded DNA.
inferredcites →https://doi.org/10.1016/s0092-8674(00)81876-0openalex-snapshot
Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family
inferredcites →https://doi.org/10.1016/s1097-2765(04)00034-6openalex-snapshot
Association of Mre11p with Double-Strand Break Sites during Yeast Meiosis
inferredcites →https://doi.org/10.1038/386414a0openalex-snapshot
An atypical topoisomerase II from archaea with implications for meiotic recombination
inferredcites →https://doi.org/10.1038/nature03872openalex-snapshot
Endonucleolytic processing of covalent protein-linked DNA double-strand breaks
inferredcites →https://doi.org/10.1038/nature04885openalex-snapshot
Clarifying the mechanics of DNA strand exchange in meiotic recombination
inferredcites →https://doi.org/10.1038/nature06337openalex-snapshot
Human CtIP promotes DNA end resection
inferredcites →https://doi.org/10.1038/nature07312openalex-snapshot
Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break processing
inferredcites →https://doi.org/10.1038/nature08444openalex-snapshot
A human 5′-tyrosyl DNA phosphodiesterase that repairs topoisomerase-mediated DNA damage
inferredcites →https://doi.org/10.1038/nature10508openalex-snapshot
ATM controls meiotic double-strand-break formation
inferredcites →https://doi.org/10.1038/nature10515openalex-snapshot
Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1
inferredcites →https://doi.org/10.1038/nature13120openalex-snapshot
Homologue engagement controls meiotic DNA break number and distribution
inferredcites →https://doi.org/10.1038/nature13771openalex-snapshot
Sae2 promotes dsDNA endonuclease activity within Mre11–Rad50–Xrs2 to resect DNA breaks
inferredcites →https://doi.org/10.1038/nature13993openalex-snapshot
Tel1ATM-mediated interference suppresses clustered meiotic double-strand-break formation
inferredcites →https://doi.org/10.1038/nrm.2016.111openalex-snapshot
Roles of eukaryotic topoisomerases in transcription, replication and genomic stability
inferredcites →https://doi.org/10.1038/nrm3047openalex-snapshot
The MRE11 complex: starting from the ends
inferredcites →https://doi.org/10.1038/nsmb.2418openalex-snapshot
Mechanism of repair of 5′-topoisomerase II–DNA adducts by mammalian tyrosyl-DNA phosphodiesterase 2
inferredcites →https://doi.org/10.1038/nsmb.2423openalex-snapshot
Structural basis for recognition of 5′-phosphotyrosine adducts by Tdp2
inferredcites →https://doi.org/10.1038/sj.emboj.7601916openalex-snapshot
A conserved function for a Caenorhabditis elegans Com1/Sae2/CtIP protein homolog in meiotic recombination
inferredcites →https://doi.org/10.1073/pnas.0603455103openalex-snapshot
Tyrosyl-DNA phosphodiesterase (Tdp1) participates in the repair of Top2-mediated DNA damage
inferredcites →https://doi.org/10.1073/pnas.1305166110openalex-snapshot
Relationship of DNA degradation by Saccharomyces cerevisiae Exonuclease 1 and its stimulation by RPA and Mre11-Rad50-Xrs2 to DNA end resection
inferredcites →https://doi.org/10.1073/pnas.92.24.11274openalex-snapshot
Covalent protein-DNA complexes at the 5' strand termini of meiosis-specific double-strand breaks in yeast.
inferredcites →https://doi.org/10.1073/pnas.93.21.11534openalex-snapshot
A eukaryotic enzyme that can disjoin dead-end covalent complexes between DNA and type I topoisomerases.
inferredcites →https://doi.org/10.1074/jbc.m000531200openalex-snapshot
TTRAP, a Novel Protein That Associates with CD40, Tumor Necrosis Factor (TNF) Receptor-75 and TNF Receptor-associated Factors (TRAFs), and That Inhibits Nuclear Factor-κB Activation
inferredcites →https://doi.org/10.1074/jbc.m114.565374openalex-snapshot
Proteolytic Degradation of Topoisomerase II (Top2) Enables the Processing of Top2·DNA and Top2·RNA Covalent Complexes by Tyrosyl-DNA-Phosphodiesterase 2 (TDP2)
inferredcites →https://doi.org/10.1091/mbc.11.7.2221openalex-snapshot
Exo1 Roles for Repair of DNA Double-Strand Breaks and Meiotic Crossing Over inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/emboj/18.21.6177openalex-snapshot
Structure and function of an archaeal topoisomerase VI subunit with homology to the meiotic recombination factor Spo11
inferredcites →https://doi.org/10.1093/genetics/146.3.781openalex-snapshot
Isolation of COM1, a New Gene Required to Complete Meiotic Double-Strand Break-Induced Recombination in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/genetics/146.3.797openalex-snapshot
A General Method for Identifying Recessive Diploid-Specific Mutations in Saccharomyces cerevisiae, Its Application to the Isolation of Mutants Blocked at Intermediate Stages of Meiotic Prophase and Characterization of a New Gene SAE2
inferredcites →https://doi.org/10.1098/rsob.130019openalex-snapshot
Positive regulation of meiotic DNA double-strand break formation by activation of the DNA damage checkpoint kinase Mec1(ATR)
inferredcites →https://doi.org/10.1101/cshperspect.a016634openalex-snapshot
Mechanism and Regulation of Meiotic Recombination Initiation
inferredcites →https://doi.org/10.1101/gad.307900.117openalex-snapshot
Plasticity of the Mre11–Rad50–Xrs2–Sae2 nuclease ensemble in the processing of DNA-bound obstacles
inferredcites →https://doi.org/10.1101/gad.308254.117openalex-snapshot
Physiological protein blocks direct the Mre11–Rad50–Xrs2 and Sae2 nuclease complex to initiate DNA end resection
inferredcites →https://doi.org/10.1124/mol.107.044651openalex-snapshot
Enhancing Drug Accumulation in Saccharomyces cerevisiae by Repression of Pleiotropic Drug Resistance Genes with Chimeric Transcription Repressors
inferredcites →https://doi.org/10.1126/science.aad5196openalex-snapshot
A DNA topoisomerase VI–like complex initiates meiotic recombination
inferredcites →https://doi.org/10.1126/science.aad5309openalex-snapshot
The TopoVIB-Like protein family is required for meiotic DNA double-strand break formation
inferredcites →https://doi.org/10.1126/science.aam6468openalex-snapshot
ZATT (ZNF451)–mediated resolution of topoisomerase 2 DNA-protein cross-links
inferredcites →https://doi.org/10.1128/jb.118.1.8-14.1974openalex-snapshot
Carbohydrate Metabolism During Ascospore Development in Yeast
inferredcites →https://doi.org/10.1128/mcb.00088-09openalex-snapshot
Locally, Meiotic Double-Strand Breaks Targeted by Gal4BD-Spo11 Occur at Discrete Sites with a Sequence Preference
inferredcites →https://doi.org/10.1128/mcb.01182-08openalex-snapshot
Ctp1CtIP and Rad32Mre11 Nuclease Activity Are Required for Rec12Spo11 Removal, but Rec12Spo11 Removal Is Dispensable for Other MRN-Dependent Meiotic Functions
inferredcites →https://doi.org/10.1371/journal.pgen.1000267openalex-snapshot
Indistinguishable Landscapes of Meiotic DNA Breaks in rad50+ and rad50S Strains of Fission Yeast Revealed by a Novel rad50+ Recombination Intermediate
inferredcites →https://doi.org/10.1371/journal.pgen.1000722openalex-snapshot
Ctp1 and the MRN-Complex Are Required for Endonucleolytic Rec12 Removal with Release of a Single Class of Oligonucleotides in Fission Yeast
inferredcites →https://doi.org/10.1371/journal.pgen.1003276openalex-snapshot
COM-1 Promotes Homologous Recombination during Caenorhabditis elegans Meiosis by Antagonizing Ku-Mediated Non-Homologous End Joining
inferredcites →https://doi.org/10.1534/genetics.105.049478openalex-snapshot
Mutations in Mre11 Phosphoesterase Motif I That Impair Saccharomyces cerevisiae Mre11-Rad50-Xrs2 Complex Stability in Addition to Nuclease Activity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.cell.2021.10.025openalex-snapshot
De novo deletions and duplications at recombination hotspots in mouse germlines
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.11.006openalex-snapshot
GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability
inferred← citeshttps://doi.org/10.1038/s41467-019-12802-5openalex-snapshot
A nucleotide resolution map of Top2-linked DNA breaks in the yeast and human genome
inferred← citeshttps://doi.org/10.1038/s41586-021-03389-3openalex-snapshot
Concerted cutting by Spo11 illuminates meiotic DNA break mechanics
inferred← citeshttps://doi.org/10.1101/2020.06.23.168138openalex-snapshot
De novo deletions and duplications at recombination hotspots in mouse germlines
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