DNA-damage tolerance mediated by PCNA•Ub fusions in human cells is dependent on Rev1 but not Polη
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Title
DNA-damage tolerance mediated by PCNA•Ub fusions in human cells is dependent on Rev1 but not Polη
Authors
Keywords
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Journal
NUCLEIC ACIDS RESEARCH
Volume 41, Issue 15, Pages 7356-7369
Publisher
Oxford University Press (OUP)
Online
2013-06-13
DOI
10.1093/nar/gkt542
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Note: Only part of the references are listed.- The Vital Role of Polymerase ζ and REV1 in Mutagenic, but Not Correct, DNA Synthesis across Benzo[a]pyrene-dG and Recruitment of Polymerase ζ by REV1 to Replication-stalled Site
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- DNA Polymerase δ and ζ Switch by Sharing Accessory Subunits of DNA Polymerase δ
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- A four-subunit DNA polymerase ζ complex containing Pol δ accessory subunits is essential for PCNA-mediated mutagenesis
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- Pol31 and Pol32 subunits of yeast DNA polymerase are also essential subunits of DNA polymerase
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- The Non-canonical Protein Binding Site at the Monomer-Monomer Interface of Yeast Proliferating Cell Nuclear Antigen (PCNA) Regulates the Rev1-PCNA Interaction and Polζ/Rev1-dependent Translesion DNA Synthesis
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- PCNA Ubiquitination Is Important, But Not Essential for Translesion DNA Synthesis in Mammalian Cells
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- Ubiquitin-PCNA fusion as a mimic for mono-ubiquitinated PCNA in Schizosaccharomyces pombe
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- Y-family DNA polymerases in mammalian cells
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- Interaction with DNA polymerase η is required for nuclear accumulation of REV1 and suppression of spontaneous mutations in human cells
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- DNA polymerase ζ cooperates with polymerases κ and ι in translesion DNA synthesis across pyrimidine photodimers in cells from XPV patients
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- RAD18 and associated proteins are immobilized in nuclear foci in human cells entering S-phase with ultraviolet light-induced damage
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