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TRF1 prevents permissive DNA damage response, recombination and Break Induced Replication at telomeres

https://doi.org/10.1101/697979
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/047120918x.emb1396openalex-snapshot
Semi‐Conservative DNA Replication
inferredcites →https://doi.org/10.1007/3-540-30683-8_54openalex-snapshot
Alternative Lengthening of Telomeres
inferredcites →https://doi.org/10.1007/978-1-4939-6892-3_3openalex-snapshot
Telomere Length Analysis by Quantitative Fluorescent In situ Hybridization (Q-FISH)
inferredcites →https://doi.org/10.1016/0014-4827(86)90583-5openalex-snapshot
Structural organizations of replicon domains during DNA synthetic phase in the mammalian nucleus
inferredcites →https://doi.org/10.1016/j.cell.2008.11.045openalex-snapshot
Purification of Proteins Associated with Specific Genomic Loci
inferredcites →https://doi.org/10.1016/j.cell.2009.06.021openalex-snapshot
Mammalian Telomeres Resemble Fragile Sites and Require TRF1 for Efficient Replication
inferredcites →https://doi.org/10.1016/j.cell.2012.03.030openalex-snapshot
RTEL1 Dismantles T Loops and Counteracts Telomeric G4-DNA to Maintain Telomere Integrity
inferredcites →https://doi.org/10.1016/j.cell.2012.05.026openalex-snapshot
Telomeric 3′ Overhangs Derive from Resection by Exo1 and Apollo and Fill-In by POT1b-Associated CST
inferredcites →https://doi.org/10.1016/j.cell.2015.01.044openalex-snapshot
Nuclear-Receptor-Mediated Telomere Insertion Leads to Genome Instability in ALT Cancers
inferredcites →https://doi.org/10.1016/j.cell.2017.11.047openalex-snapshot
Stabilization of Reversed Replication Forks by Telomerase Drives Telomere Catastrophe
inferredcites →https://doi.org/10.1016/j.celrep.2014.07.024openalex-snapshot
A Macrohistone Variant Links Dynamic Chromatin Compaction to BRCA1-Dependent Genome Maintenance
inferredcites →https://doi.org/10.1016/j.celrep.2015.10.041openalex-snapshot
ATM and ATR Signaling Regulate the Recruitment of Human Telomerase to Telomeres
inferredcites →https://doi.org/10.1016/j.celrep.2016.01.011openalex-snapshot
SMARCAL1 Resolves Replication Stress at ALT Telomeres
inferredcites →https://doi.org/10.1016/j.celrep.2016.05.077openalex-snapshot
Rif1 Regulates the Fate of DNA Entanglements during Mitosis
inferredcites →https://doi.org/10.1016/j.celrep.2016.10.048openalex-snapshot
Proteomic Profiling Reveals a Specific Role for Translesion DNA Polymerase η in the Alternative Lengthening of Telomeres
inferredcites →https://doi.org/10.1016/j.molcel.2009.06.025openalex-snapshot
TERRA RNA Binding to TRF2 Facilitates Heterochromatin Formation and ORC Recruitment at Telomeres
inferredcites →https://doi.org/10.1016/j.molcel.2016.10.037openalex-snapshot
RAD52 Facilitates Mitotic DNA Synthesis Following Replication Stress
inferredcites →https://doi.org/10.1016/j.molcel.2016.10.038openalex-snapshot
Mammalian RAD52 Functions in Break-Induced Replication Repair of Collapsed DNA Replication Forks
inferredcites →https://doi.org/10.1016/j.tcb.2013.11.007openalex-snapshot
Structure-specific endonucleases: guardians of fragile site stability
inferredcites →https://doi.org/10.1038/emboj.2012.96openalex-snapshot
CTC1 deletion results in defective telomere replication, leading to catastrophic telomere loss and stem cell exhaustion
inferredcites →https://doi.org/10.1038/nature04638openalex-snapshot
Semi-conservative DNA replication through telomeres requires Taz1
inferredcites →https://doi.org/10.1038/nature16139openalex-snapshot
Replication stress activates DNA repair synthesis in mitosis
inferredcites →https://doi.org/10.1038/nature20099openalex-snapshot
Break-induced telomere synthesis underlies alternative telomere maintenance
inferredcites →https://doi.org/10.1038/ncb1685openalex-snapshot
Developmentally regulated transcription of mammalian telomeres by DNA-dependent RNA polymerase II
inferredcites →https://doi.org/10.1038/ncomms6220openalex-snapshot
RNaseH1 regulates TERRA-telomeric DNA hybrids and telomere maintenance in ALT tumour cells
inferredcites →https://doi.org/10.1038/nm1197-1271openalex-snapshot
Evidence for an alternative mechanism for maintaining telomere length in human tumors and tumor-derived cell lines
inferredcites →https://doi.org/10.1038/nprot.2006.468openalex-snapshot
In-gel digestion for mass spectrometric characterization of proteins and proteomes
inferredcites →https://doi.org/10.1038/nrg2763openalex-snapshot
Alternative lengthening of telomeres: models, mechanisms and implications
inferredcites →https://doi.org/10.1038/nsmb.1725openalex-snapshot
Spontaneous occurrence of telomeric DNA damage response in the absence of chromosome fusions
inferredcites →https://doi.org/10.1038/nsmb.2877openalex-snapshot
NuRD–ZNF827 recruitment to telomeres creates a molecular scaffold for homologous recombination
inferredcites →https://doi.org/10.1038/nsmb1259openalex-snapshot
The SMC5/6 complex maintains telomere length in ALT cancer cells through SUMOylation of telomere-binding proteins
inferredcites →https://doi.org/10.1038/s41594-017-0021-5openalex-snapshot
TRF1 participates in chromosome end protection by averting TRF2-dependent telomeric R loops
inferredcites →https://doi.org/10.1038/sj.emboj.7601218openalex-snapshot
Human SMC5/6 complex promotes sister chromatid homologous recombination by recruiting the SMC1/3 cohesin complex to double‐strand breaks
inferredcites →https://doi.org/10.1038/srep38873openalex-snapshot
Roles of human POLD1 and POLD3 in genome stability
inferredcites →https://doi.org/10.1073/pnas.0907689106openalex-snapshot
Probing PML body function in ALT cells reveals spatiotemporal requirements for telomere recombination
inferredcites →https://doi.org/10.1073/pnas.0908258106openalex-snapshot
Interplay between the Smc5/6 complex and the Mph1 helicase in recombinational repair
inferredcites →https://doi.org/10.1073/pnas.1708065114openalex-snapshot
FANCM, BRCA1, and BLM cooperatively resolve the replication stress at the ALT telomeres
inferredcites →https://doi.org/10.1073/pnas.85.18.6622openalex-snapshot
A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes.
inferredcites →https://doi.org/10.1074/jbc.c000390200openalex-snapshot
NBS1 and TRF1 Colocalize at Promyelocytic Leukemia Bodies during Late S/G2 Phases in Immortalized Telomerase-negative Cells
inferredcites →https://doi.org/10.1074/mcp.m113.031591openalex-snapshot
Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ
inferredcites →https://doi.org/10.1083/jcb.200908136openalex-snapshot
ATR suppresses telomere fragility and recombination but is dispensable for elongation of short telomeres by telomerase
inferredcites →https://doi.org/10.1083/jcb.201207189openalex-snapshot
Variant repeats are interspersed throughout the telomeres and recruit nuclear receptors in ALT cells
inferredcites →https://doi.org/10.1093/nar/gks407openalex-snapshot
The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures
inferredcites →https://doi.org/10.1093/nar/gky099openalex-snapshot
RNA–DNA hybrids promote the expansion of Friedreich's ataxia (GAA)n repeats via break-induced replication
inferredcites →https://doi.org/10.1093/nar/gky173openalex-snapshot
Human RTEL1 stabilizes long G-overhangs allowing telomerase-dependent over-extension
inferredcites →https://doi.org/10.1101/gad.1346005openalex-snapshot
Shelterin: the protein complex that shapes and safeguards human telomeres
inferredcites →https://doi.org/10.1101/gad.251611.114openalex-snapshot
TRF1 negotiates TTAGGG repeat-associated replication problems by recruiting the BLM helicase and the TPP1/POT1 repressor of ATR signaling
inferredcites →https://doi.org/10.1101/gad.543509openalex-snapshot
Increased telomere fragility and fusions resulting from TRF1 deficiency lead to degenerative pathologies and increased cancer in mice
inferredcites →https://doi.org/10.1126/science.1147182openalex-snapshot
Telomeric Repeat–Containing RNA and RNA Surveillance Factors at Mammalian Chromosome Ends
inferredcites →https://doi.org/10.1126/science.7605428openalex-snapshot
Specific Association of Human Telomerase Activity with Immortal Cells and Cancer
inferredcites →https://doi.org/10.1128/mcb.00226-17openalex-snapshot
Alternative Lengthening of Telomeres Mediated by Mitotic DNA Synthesis Engages Break-Induced Replication Processes
inferredcites →https://doi.org/10.1128/mcb.22.18.6384-6392.2002openalex-snapshot
Characterization of RAD51-Independent Break-Induced Replication That Acts Preferentially with Short Homologous Sequences
inferredcites →https://doi.org/10.1146/annurev-genet-120417-031353openalex-snapshot
The Smc5/6 Complex: New and Old Functions of the Enigmatic Long-Distance Relative
inferredcites →https://doi.org/10.1146/annurev.genet.41.110306.130350openalex-snapshot
How Shelterin Protects Mammalian Telomeres
inferredcites →https://doi.org/10.1371/journal.pgen.1007136openalex-snapshot
The Smc5/6 complex regulates the yeast Mph1 helicase at RNA-DNA hybrid-mediated DNA damage
inferredcites →https://doi.org/10.15252/embr.201643169openalex-snapshot
Alternative lengthening of human telomeres is a conservative DNA replication process with features of break‐induced replication
inferredcites →https://doi.org/10.3389/fonc.2013.00027openalex-snapshot
Alternative lengthening of telomeres: remodeling the telomere architecture
inferredcites →https://doi.org/10.4161/cc.28419openalex-snapshot
TopoIIα prevents telomere fragility and formation of ultra thin DNA bridges during mitosis through TRF1-dependent binding to telomeres
inferredcites →https://doi.org/10.7554/elife.20533openalex-snapshot
RNase H enables efficient repair of R-loop induced DNA damage
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