Supplemental material
Cell Cycle
Volume 14, 2015 - Issue 11
Related Research Data
A small ubiquitin binding domain inhibits ubiquitin-dependent protein recruitment to DNA repair foci
Source:
Informa UK Limited
53BP1 facilitates long-range DNA end-joining during V(D)J recombination
Source:
Springer Science and Business Media LLC
A novel ubiquitin mark at the N-terminal tail of histone H2As targeted by RNF168 ubiquitin ligase
Source:
Informa UK Limited
ATM and related protein kinases: safeguarding genome integrity
Source:
Springer Science and Business Media LLC
DNA double-strand break repair
Source:
Elsevier BV
Ubiquitin-activating enzyme UBA1 is required for cellular response to DNA damage
Source:
Informa UK Limited
Potential role for 53BP1 in DNA end-joining repair through direct interaction with DNA.
Source:
Elsevier BV
γH2AX and MDC1: Anchoring the DNA-damage-response machinery to broken chromosomes
Source:
Elsevier BV
Rap80 Protein Recruitment to DNA Double-strand Breaks Requires Binding to Both Small Ubiquitin-like Modifier (SUMO) and Ubiquitin Conjugates
Source:
American Society for Biochemistry & Molecular Biology (ASBMB)
A dynamic ubiquitin equilibrium couples proteasomal activity to chromatin remodeling
Source:
Rockefeller University Press
Histone H2B ubiquitylation disrupts local and higher-order chromatin compaction
Source:
Springer Nature
Histone H4 deacetylation facilitates 53BP1 DNA damage signaling and double-strand break repair
Source:
Oxford University Press (OUP)
RNF168 Binds and Amplifies Ubiquitin Conjugates on Damaged Chromosomes to Allow Accumulation of Repair Proteins
Source:
Elsevier Inc.
The p400 ATPase regulates nucleosome stability and chromatin ubiquitination during DNA repair
Source:
Rockefeller University Press
The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage
Source:
Elsevier BV
Ubiquitin-H2AX fusions render 53BP1 recruitment to DNA damage sites independent of RNF8 or RNF168
Source:
Figshare
Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response.
Source:
American Association for the Advancement of Science (AAAS)
Regulation and mechanisms of mammalian double-strand break repair
Source:
Springer Science and Business Media LLC
RIF1 Is Essential for 53BP1-Dependent Nonhomologous End Joining and Suppression of DNA Double-Strand Break Resection
Source:
Elsevier BV
53BP1: function and mechanisms of focal recruitment
Source:
Portland Press Ltd.
53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers
Source:
Springer Nature
Cell-cycle checkpoints and cancer
Source:
Springer Science and Business Media LLC
DNA damage-induced G2-M checkpoint activation by histone H2AX and 53BP1.
Source:
Springer Science and Business Media LLC
BRCT Domain Interactions with Phospho-Histone H2A Target Crb2 to Chromatin at Double-Strand Breaks and Maintain the DNA Damage Checkpoint
Source:
American Society for Microbiology
53BP1 Regulates DSB Repair Using Rif1 to Control 5' End Resection
Source:
American Association for the Advancement of Science (AAAS)
JMJD1C demethylates MDC1 to regulate the RNF8 and BRCA1–mediated chromatin response to DNA breaks
Source:
Springer Nature
Impact of Histone H4 Lysine 20 Methylation on 53BP1 Responses to Chromosomal Double Strand Breaks
Source:
Public Library of Science (PLoS)
Orchestration of the DNA-Damage Response by the RNF8 Ubiquitin Ligase
Source:
American Association for the Advancement of Science (AAAS)
ATM signaling and 53BP1
Source:
Elsevier BV
P53 Binding Protein 1 (53bp1) Is an Early Participant in the Cellular Response to DNA Double-Strand Breaks
Source:
Rockefeller University Press
MDC1 is a mediator of the mammalian DNA damage checkpoint
Source:
Springer Nature
BRCA1-associated exclusion of 53BP1 from DNA damage sites underlies temporal control of DNA repair
Source:
The Company of Biologists
Structural Basis for the Methylation State-Specific Recognition of Histone H4-K20 by 53BP1 and Crb2 in DNA Repair
Source:
Elsevier Inc.
53BP1 Inhibits Homologous Recombination in Brca1-Deficient Cells by Blocking Resection of DNA Breaks
Source:
Elsevier BV
RNF8 Transduces the DNA-Damage Signal via Histone Ubiquitylation and Checkpoint Protein Assembly.
Source:
Elsevier BV
BRCA1 Functions Independently of Homologous Recombination in DNA Interstrand Crosslink Repair
Source:
Elsevier BV
53BP1 functions in an ATM-dependent checkpoint pathway that is constitutively activated in human cancer
Source:
Springer Science and Business Media LLC
Rif1 Prevents Resection of DNA Breaks and Promotes Immunoglobulin Class Switching
Source:
American Association for the Advancement of Science (AAAS)
A Cell Cycle-Dependent Regulatory Circuit Composed of 53BP1-RIF1 and BRCA1-CtIP Controls DNA Repair Pathway Choice
Source:
Elsevier BV
RNF168, a new RING finger, MIU-containing protein that modifies chromatin by ubiquitination of histones H2A and H2AX
Source:
Springer Nature
Bat3 facilitates H3K79 dimethylation by DOT1L and promotes DNA damage-induced 53BP1 foci at G1/G2 cell-cycle phases
Source:
Wiley-Blackwell
53BP1 is a reader of the DNA-damage-induced H2A Lys 15 ubiquitin mark
Source:
Springer Science and Business Media LLC
Tudor domains track down DNA breaks
Source:
Springer Nature
RAP80 Targets BRCA1 to Specific Ubiquitin Structures at DNA Damage Sites
Source:
American Association for the Advancement of Science (AAAS)
Ubiquitin-H2AX fusions render 53BP1 recruitment to DNA damage sites independent of RNF8 or RNF168
Source:
Figshare
Ring1-mediated ubiquitination of H2A restrains poised RNA polymerase II at bivalent genes in mouse ES cells
Source:
Springer Nature
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