Literature DB >> 21376743

Choosing the right path: does DNA-PK help make the decision?

Jessica A Neal1, Katheryn Meek.   

Abstract

DNA double-strand breaks are extremely harmful lesions that can lead to genomic instability and cell death if not properly repaired. There are at least three pathways that are responsible for repairing DNA double-strand breaks in mammalian cells: non-homologous end joining, homologous recombination and alternative non-homologous end joining. Here we review each of these three pathways with an emphasis on the role of the DNA-dependent protein kinase, a critical component of the non-homologous end joining pathway, in influencing which pathway is ultimately utilized for repair. 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21376743      PMCID: PMC3109507          DOI: 10.1016/j.mrfmmm.2011.02.010

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  178 in total

1.  Transient stability of DNA ends allows nonhomologous end joining to precede homologous recombination.

Authors:  Marie Frank-Vaillant; Stéphane Marcand
Journal:  Mol Cell       Date:  2002-11       Impact factor: 17.970

2.  Absence of DNA ligase IV protein in XR-1 cells: evidence for stabilization by XRCC4.

Authors:  M Bryans; M C Valenzano; T D Stamato
Journal:  Mutat Res       Date:  1999-01-26       Impact factor: 2.433

3.  Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells.

Authors:  U Grawunder; M Wilm; X Wu; P Kulesza; T E Wilson; M Mann; M R Lieber
Journal:  Nature       Date:  1997-07-31       Impact factor: 49.962

4.  Identification, characterization, and genetic mapping of Rad51d, a new mouse and human RAD51/RecA-related gene.

Authors:  D L Pittman; L R Weinberg; J C Schimenti
Journal:  Genomics       Date:  1998-04-01       Impact factor: 5.736

5.  Extrachromosomal DNA substrates in pre-B cells undergo inversion or deletion at immunoglobulin V-(D)-J joining signals.

Authors:  J E Hesse; M R Lieber; M Gellert; K Mizuuchi
Journal:  Cell       Date:  1987-06-19       Impact factor: 41.582

6.  Inhibition of homologous recombination by DNA-dependent protein kinase requires kinase activity, is titratable, and is modulated by autophosphorylation.

Authors:  Jessica A Neal; Van Dang; Pauline Douglas; Marc S Wold; Susan P Lees-Miller; Katheryn Meek
Journal:  Mol Cell Biol       Date:  2011-02-07       Impact factor: 4.272

7.  The DNA-dependent protein kinase is inactivated by autophosphorylation of the catalytic subunit.

Authors:  D W Chan; S P Lees-Miller
Journal:  J Biol Chem       Date:  1996-04-12       Impact factor: 5.157

8.  Defects in XRCC4 and KU80 differentially affect the joining of distal nonhomologous ends.

Authors:  Josée Guirouilh-Barbat; Emilie Rass; Isabelle Plo; Pascale Bertrand; Bernard S Lopez
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-18       Impact factor: 11.205

9.  Lymphocyte-specific compensation for XLF/cernunnos end-joining functions in V(D)J recombination.

Authors:  Gang Li; Frederick W Alt; Hwei-Ling Cheng; James W Brush; Peter H Goff; Mike M Murphy; Sonia Franco; Yu Zhang; Shan Zha
Journal:  Mol Cell       Date:  2008-09-05       Impact factor: 17.970

10.  53BP1 is required for class switch recombination.

Authors:  Irene M Ward; Bernardo Reina-San-Martin; Alexandru Olaru; Kay Minn; Koji Tamada; Julie S Lau; Marilia Cascalho; Lieping Chen; Andre Nussenzweig; Ferenc Livak; Michel C Nussenzweig; Junjie Chen
Journal:  J Cell Biol       Date:  2004-05-24       Impact factor: 10.539

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  53 in total

1.  Robust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1).

Authors:  Cristian Boboila; Valentyn Oksenych; Monica Gostissa; Jing H Wang; Shan Zha; Yu Zhang; Hua Chai; Cheng-Sheng Lee; Mila Jankovic; Liz-Marie Albertorio Saez; Michel C Nussenzweig; Peter J McKinnon; Frederick W Alt; Bjoern Schwer
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-30       Impact factor: 11.205

2.  Unraveling the complexities of DNA-dependent protein kinase autophosphorylation.

Authors:  Jessica A Neal; Seiji Sugiman-Marangos; Pamela VanderVere-Carozza; Mike Wagner; John Turchi; Susan P Lees-Miller; Murray S Junop; Katheryn Meek
Journal:  Mol Cell Biol       Date:  2014-03-31       Impact factor: 4.272

Review 3.  Cellular stress response and innate immune signaling: integrating pathways in host defense and inflammation.

Authors:  Sujatha Muralidharan; Pranoti Mandrekar
Journal:  J Leukoc Biol       Date:  2013-08-29       Impact factor: 4.962

Review 4.  Structural insights into NHEJ: building up an integrated picture of the dynamic DSB repair super complex, one component and interaction at a time.

Authors:  Gareth J Williams; Michal Hammel; Sarvan Kumar Radhakrishnan; Dale Ramsden; Susan P Lees-Miller; John A Tainer
Journal:  DNA Repair (Amst)       Date:  2014-03-20

Review 5.  The ATM protein kinase: regulating the cellular response to genotoxic stress, and more.

Authors:  Yosef Shiloh; Yael Ziv
Journal:  Nat Rev Mol Cell Biol       Date:  2013-03-13       Impact factor: 94.444

Review 6.  Detection and repair of ionizing radiation-induced DNA double strand breaks: new developments in nonhomologous end joining.

Authors:  Chen Wang; Susan P Lees-Miller
Journal:  Int J Radiat Oncol Biol Phys       Date:  2013-02-20       Impact factor: 7.038

Review 7.  Repair of double-strand breaks by end joining.

Authors:  Kishore K Chiruvella; Zhuobin Liang; Thomas E Wilson
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-05-01       Impact factor: 10.005

Review 8.  Non-homologous end joining: emerging themes and unanswered questions.

Authors:  Sarvan Kumar Radhakrishnan; Nicholas Jette; Susan P Lees-Miller
Journal:  DNA Repair (Amst)       Date:  2014-02-26

Review 9.  Role of AKT signaling in DNA repair and clinical response to cancer therapy.

Authors:  Qun Liu; Kristen M Turner; W K Alfred Yung; Kexin Chen; Wei Zhang
Journal:  Neuro Oncol       Date:  2014-05-07       Impact factor: 12.300

Review 10.  XRCC4 and XLF form long helical protein filaments suitable for DNA end protection and alignment to facilitate DNA double strand break repair.

Authors:  Brandi L Mahaney; Michal Hammel; Katheryn Meek; John A Tainer; Susan P Lees-Miller
Journal:  Biochem Cell Biol       Date:  2013-02-05       Impact factor: 3.626

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