Alternative end-joining catalyzes robust IgH locus deletions and translocations in the combined absence of ligase 4 and Ku70
about
Alternative end-joining mechanisms: a historical perspectiveDNA ligase III promotes alternative nonhomologous end-joining during chromosomal translocation formationRobust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1)Alternative Okazaki Fragment Ligation Pathway by DNA Ligase IIIDNA double-strand break repair pathway choice and cancerRelated Mechanisms of Antibody Somatic Hypermutation and Class Switch Recombination53BP1 mediates productive and mutagenic DNA repair through distinct phosphoprotein interactions.Snaps and mends: DNA breaks and chromosomal translocationsHomology and enzymatic requirements of microhomology-dependent alternative end joiningDNA ligases I and III cooperate in alternative non-homologous end-joining in vertebratesWRN regulates pathway choice between classical and alternative non-homologous end joiningGenomic stability in response to high versus low linear energy transfer radiation in Arabidopsis thaliana.Generation and repair of AID-initiated DNA lesions in B lymphocytes.Downstream class switching leads to IgE antibody production by B lymphocytes lacking IgM switch regions.53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination.Origin of chromosomal translocations in lymphoid cancer.Regulation of immunoglobulin class-switch recombination: choreography of noncoding transcription, targeted DNA deamination, and long-range DNA repair.Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions.Polo-like kinase 3 regulates CtIP during DNA double-strand break repair in G1.Induction of DNA damage and erroneous repair can explain genomic instability caused by endosulfan.AID-initiated DNA lesions are differentially processed in distinct B cell populations.Comparison of constitutional and replication stress-induced genome structural variation by SNP array and mate-pair sequencingMismatch repair proteins MSH2, MLH1, and EXO1 are important for class-switch recombination events occurring in B cells that lack nonhomologous end joining.ATM release at resected double-strand breaks provides heterochromatin reconstitution to facilitate homologous recombination.Regulation of DNA end joining, resection, and immunoglobulin class switch recombination by 53BP1.Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cellsOn the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining.Human Mre11/human Rad50/Nbs1 and DNA ligase IIIalpha/XRCC1 protein complexes act together in an alternative nonhomologous end joining pathwayXRCC1 suppresses somatic hypermutation and promotes alternative nonhomologous end joining in Igh genes.Parp3 negatively regulates immunoglobulin class switch recombination.An essential role for CtIP in chromosomal translocation formation through an alternative end-joining pathwayNbs1 ChIP-Seq Identifies Off-Target DNA Double-Strand Breaks Induced by AID in Activated Splenic B Cells.Functional redundancy between repair factor XLF and damage response mediator 53BP1 in V(D)J recombination and DNA repair.X-ray repair cross-complementing protein 1 (XRCC1) deficiency enhances class switch recombination and is permissive for alternative end joining.Rapid analysis of chromosome aberrations in mouse B lymphocytes by PNA-FISH.Initiation of DNA double strand break repair: signaling and single-stranded resection dictate the choice between homologous recombination, non-homologous end-joining and alternative end-joiningDNA ligase I is not essential for mammalian cell viability.Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing.53BP1 Protects against CtIP-Dependent Capture of Ectopic Chromosomal Sequences at the Junction of Distant Double-Strand Breaks.
P2860
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P2860
Alternative end-joining catalyzes robust IgH locus deletions and translocations in the combined absence of ligase 4 and Ku70
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@ast
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@en
type
label
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@ast
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@en
prefLabel
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@ast
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@en
P2093
P2860
P356
P1476
Alternative end-joining cataly ...... d absence of ligase 4 and Ku70
@en
P2093
Alex Fazeli
Andre Nussenzweig
Catherine T Yan
Cristian Boboila
Duane R Wesemann
Frederick W Alt
Jing H Wang
Lauren Feldman
Mila Jankovic
Tingting Zhang
P2860
P304
P356
10.1073/PNAS.0915067107
P407
P577
2010-01-25T00:00:00Z