Literature DB >> 23063072

Classical and alternative end-joining pathways for repair of lymphocyte-specific and general DNA double-strand breaks.

Cristian Boboila1, Frederick W Alt, Bjoern Schwer.   

Abstract

Classical nonhomologous end joining (C-NHEJ) is one of the two major known pathways for the repair of DNA double-strand breaks (DSBs) in mammalian cells. Our understanding of C-NHEJ has been derived, in significant part, through studies of programmed physiologic DNA DSBs formed during V(D)J recombination in the developing immune system. Studies of immunoglobulin heavy-chain (IgH) class-switch recombination (CSR) also have revealed that there is an "alternative" end-joining process (A-EJ) that can function, relatively robustly, in the repair of DSBs in activated mature B lymphocytes. This A-EJ process has also been implicated in the formation of oncogenic translocations found in lymphoid tumors. In this review, we discuss our current understanding of C-NHEJ and A-EJ in the context of V(D)J recombination, CSR, and the formation of chromosomal translocations.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2012        PMID: 23063072     DOI: 10.1016/B978-0-12-394300-2.00001-6

Source DB:  PubMed          Journal:  Adv Immunol        ISSN: 0065-2776            Impact factor:   3.543


  138 in total

1.  DNA polymerases δ and λ cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiae.

Authors:  Damon Meyer; Becky Xu Hua Fu; Wolf-Dietrich Heyer
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-25       Impact factor: 11.205

2.  Transcription-associated processes cause DNA double-strand breaks and translocations in neural stem/progenitor cells.

Authors:  Bjoern Schwer; Pei-Chi Wei; Amelia N Chang; Jennifer Kao; Zhou Du; Robin M Meyers; Frederick W Alt
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-12       Impact factor: 11.205

3.  DNA double-strand break response factors influence end-joining features of IgH class switch and general translocation junctions.

Authors:  Rohit A Panchakshari; Xuefei Zhang; Vipul Kumar; Zhou Du; Pei-Chi Wei; Jennifer Kao; Junchao Dong; Frederick W Alt
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-08       Impact factor: 11.205

4.  Assembly Pathway and Characterization of the RAG1/2-DNA Paired and Signal-end Complexes.

Authors:  Mikalai Lapkouski; Watchalee Chuenchor; Min-Sung Kim; Martin Gellert; Wei Yang
Journal:  J Biol Chem       Date:  2015-04-22       Impact factor: 5.157

5.  p53 and the PWWP domain containing effector proteins in chromatin damage repair.

Authors:  Jing Hu; Yanming Wang
Journal:  Cell Dev Biol       Date:  2013-05-10

Review 6.  Double-strand break repair: 53BP1 comes into focus.

Authors:  Stephanie Panier; Simon J Boulton
Journal:  Nat Rev Mol Cell Biol       Date:  2013-12-11       Impact factor: 94.444

Review 7.  BRCA1 Mutation: A Predictive Marker for Radiation Therapy?

Authors:  Charlene Kan; Junran Zhang
Journal:  Int J Radiat Oncol Biol Phys       Date:  2015-10-01       Impact factor: 7.038

8.  C-terminal region of activation-induced cytidine deaminase (AID) is required for efficient class switch recombination and gene conversion.

Authors:  Somayeh Sabouri; Maki Kobayashi; Nasim A Begum; Jianliang Xu; Kouji Hirota; Tasuku Honjo
Journal:  Proc Natl Acad Sci U S A       Date:  2014-01-27       Impact factor: 11.205

9.  A role for XLF in DNA repair and recombination in human somatic cells.

Authors:  Farjana Jahan Fattah; Junghun Kweon; Yongbao Wang; Eu Han Lee; Yinan Kan; Natalie Lichter; Natalie Weisensel; Eric A Hendrickson
Journal:  DNA Repair (Amst)       Date:  2014-01-21

Review 10.  The convergence of DNA damage checkpoint pathways and androgen receptor signaling in prostate cancer.

Authors:  Huy Q Ta; Daniel Gioeli
Journal:  Endocr Relat Cancer       Date:  2014-08-05       Impact factor: 5.678

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.