Polyubiquitinated PCNA recruits the ZRANB3 translocase to maintain genomic integrity after replication stress
about
Nucleotide excision repair is associated with the replisome and its efficiency depends on a direct interaction between XPA and PCNACBP and p300 acetylate PCNA to link its degradation with nucleotide excision repair synthesisPRP19 transforms into a sensor of RPA-ssDNA after DNA damage and drives ATR activation via a ubiquitin-mediated circuitryThe helicase FBH1 is tightly regulated by PCNA via CRL4(Cdt2)-mediated proteolysis in human cellsReplication-Associated Recombinational Repair: Lessons from Budding YeastThe Regulation of DNA Damage Tolerance by Ubiquitin and Ubiquitin-Like ModifiersFunctions of Ubiquitin and SUMO in DNA Replication and Replication StressInhibition of Topoisomerase (DNA) I (TOP1): DNA Damage Repair and Anticancer TherapyPeeling away the layers of ubiquitin signaling complexities with synthetic ubiquitin-protein conjugates.Replication stress: getting back on trackPreventing replication fork collapse to maintain genome integrityIdentification and characterization of SMARCAL1 protein complexesThe transcription factor TFII-I promotes DNA translesion synthesis and genomic stabilityStructure and specificity of the bacterial cysteine methyltransferase effector NleE suggests a novel substrate in human DNA repair pathwayRole of PCNA and TLS polymerases in D-loop extension during homologous recombination in humansHuman HLTF mediates postreplication repair by its HIRAN domain-dependent replication fork remodelling.Structure of a Novel DNA-binding Domain of Helicase-like Transcription Factor (HLTF) and Its Functional Implication in DNA Damage ToleranceIdentification of a Substrate Recognition Domain in the Replication Stress Response Protein Zinc Finger Ran-binding Domain-containing Protein 3 (ZRANB3).Visualization of recombination-mediated damage bypass by template switching.Substrate-selective repair and restart of replication forks by DNA translocasesTreacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response.Targeting proliferating cell nuclear antigen and its protein interactions induces apoptosis in multiple myeloma cells.Single cell analysis of human RAD18-dependent DNA post-replication repair by alkaline bromodeoxyuridine comet assay.Increased Anticancer Efficacy of Intravesical Mitomycin C Therapy when Combined with a PCNA Targeting Peptide.A recessive variant of XRCC4 predisposes to non- BRCA1/2 breast cancer in chinese women and impairs the DNA damage response via dysregulated nuclear localizationRad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells.The annealing helicase and branch migration activities of Drosophila HARP.Regulation of DNA pairing in homologous recombination.A Systematic Analysis of Factors Localized to Damaged Chromatin Reveals PARP-Dependent Recruitment of Transcription FactorsHLTF's Ancient HIRAN Domain Binds 3' DNA Ends to Drive Replication Fork Reversal.Discrimination of Kinetic Models by a Combination of Microirradiation and Fluorescence Photobleaching.DNA damage tolerance pathway involving DNA polymerase ι and the tumor suppressor p53 regulates DNA replication fork progression.RPA-Binding Protein ETAA1 Is an ATR Activator Involved in DNA Replication Stress Response.SMARCAL1 maintains telomere integrity during DNA replication.Alpha thalassemia/mental retardation syndrome X-linked gene product ATRX is required for proper replication restart and cellular resistance to replication stress.A non-catalytic role of DNA polymerase η in recruiting Rad18 and promoting PCNA monoubiquitination at stalled replication forksATR phosphorylates SMARCAL1 to prevent replication fork collapseDNA damage tolerance: a double-edged sword guarding the genomePhosphorylation of a C-terminal auto-inhibitory domain increases SMARCAL1 activity.The interaction between ALKBH2 DNA repair enzyme and PCNA is direct, mediated by the hydrophobic pocket of PCNA and perturbed in naturally-occurring ALKBH2 variants.
P2860
Q21133901-38A88BAC-86F8-479C-8E75-BEC32EB92C84Q24299397-63B22D33-DBF7-4D22-9670-F281E83BC8F7Q24312535-1458977B-345C-4B1A-A828-9735A57B58D8Q24599645-C4A94E80-AC51-4FB4-BE64-63B0E8DB9C35Q26739929-B9E43CFB-D625-49E2-8A4E-C357F7D72F44Q26744520-EBCECE05-1DB0-4AD9-922D-B1F3E4329D5DQ26744570-F792FA05-711C-48C7-9BFD-EA528474A7A0Q26796576-45042E10-EEB2-43EF-91F0-08AC2E849C5CQ27693783-2332C0E8-85E8-46C5-9B70-57B8FEB914EDQ28067138-19227273-3B24-4818-B7A5-0B79B6B03392Q28083804-5D487328-CA57-415C-9E7B-3E830018CA28Q28487879-A00BD551-94BC-4046-9A7C-D95A6EA8E72EQ28539614-B566C134-52D8-4052-9C9C-2CC9DFAF56F1Q28545104-FDFE8600-8200-4B58-8655-B03976995EBEQ28681916-3979FE52-88AE-4646-BC79-89A0611F9F35Q29871515-C59C8AE7-695D-47AC-85A6-7BC34D13EFF4Q30373537-3837D32D-D6CE-4791-89BF-F87D185A791AQ33629544-D0366EA5-9CE8-4D1E-821A-4EE54D36FCE6Q34307346-F7B9C0D9-D3BA-4E13-BC72-27E6599F5605Q34762664-CDB479F5-C410-486A-A173-E74233695779Q34831316-20A2FA3E-F241-4AB2-B709-45B30A720293Q34922853-2EC39458-D6AD-48C7-B818-218F533A338BQ34925644-15732B30-FF1D-48C5-A1BC-AB008F58782FQ35028770-DBFEE9B3-DBBE-4E5D-8190-1B101CFBC7C2Q35067965-317BF0AE-93EA-4646-894B-024D6304611AQ35141185-01A0A404-3B23-474E-B519-AFA99DA3660BQ35174890-F12902FB-028D-4614-BE5F-7F4926ED469AQ35548968-A2CD8C4C-3ED6-4A17-A136-4A5A7A8004A9Q35640249-1FA4F885-DCA7-4888-9DEB-2E98E5F7D92DQ35762843-7E02476B-5AAF-4FD1-BA95-1937C2A20D5AQ35816088-988A3ACB-4A93-4638-AE22-6F5B80345529Q36074455-C6539CAF-6BF5-47AF-9848-C41B0B7A3E09Q36183806-B792005C-299C-4FB9-A63E-0775FD1F2C8EQ36354812-A555EECC-94EF-4F66-B4AD-58B21302EFACQ36647310-C7EE6DB0-09D4-498B-8CFD-398F610191E2Q36684819-282BC978-BE9C-4964-80A8-DC9A6B733D36Q37064611-6A45FAAA-793D-48BB-A09D-B755FD5CD8B6Q37187991-7F1DC2EB-2646-431B-9915-C6B630CAA8D5Q37518632-4DE861BB-5CEC-4D6D-A015-BEBE7FEA7662Q37550945-79ED8D39-1249-4F89-A111-C98FDD47404C
P2860
Polyubiquitinated PCNA recruits the ZRANB3 translocase to maintain genomic integrity after replication stress
description
2012 nî lūn-bûn
@nan
2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Polyubiquitinated PCNA recruit ...... grity after replication stress
@ast
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en-gb
Polyubiquitinated PCNA recruit ...... grity after replication stress
@nl
type
label
Polyubiquitinated PCNA recruit ...... grity after replication stress
@ast
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en-gb
Polyubiquitinated PCNA recruit ...... grity after replication stress
@nl
prefLabel
Polyubiquitinated PCNA recruit ...... grity after replication stress
@ast
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en-gb
Polyubiquitinated PCNA recruit ...... grity after replication stress
@nl
P2093
P2860
P921
P3181
P1433
P1476
Polyubiquitinated PCNA recruit ...... grity after replication stress
@en
P2093
Alberto Ciccia
Amitabh V Nimonkar
Britt Adamson
David M Livingston
Ildiko Hajdu
John C Yoon
Lajos Haracska
Lior Izhar
Sarah A Petit
Stephen C Kowalczykowski
P2860
P304
P3181
P356
10.1016/J.MOLCEL.2012.05.024
P407
P577
2012-08-10T00:00:00Z