Literature DB >> 29247009

Nonhomologous DNA end-joining for repair of DNA double-strand breaks.

Nicholas R Pannunzio1, Go Watanabe1, Michael R Lieber2.   

Abstract

Nonhomologous DNA end-joining (NHEJ) is the predominant double-strand break (DSB) repair pathway throughout the cell cycle and accounts for nearly all DSB repair outside of the S and G2 phases. NHEJ relies on Ku to thread onto DNA termini and thereby improve the affinity of the NHEJ enzymatic components consisting of polymerases (Pol μ and Pol λ), a nuclease (the Artemis·DNA-PKcs complex), and a ligase (XLF·XRCC4·Lig4 complex). Each of the enzymatic components is distinctive for its versatility in acting on diverse incompatible DNA end configurations coupled with a flexibility in loading order, resulting in many possible junctional outcomes from one DSB. DNA ends can either be directly ligated or, if the ends are incompatible, processed until a ligatable configuration is achieved that is often stabilized by up to 4 bp of terminal microhomology. Processing of DNA ends results in nucleotide loss or addition, explaining why DSBs repaired by NHEJ are rarely restored to their original DNA sequence. Thus, NHEJ is a single pathway with multiple enzymes at its disposal to repair DSBs, resulting in a diversity of repair outcomes.
© 2018 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  DNA endonuclease; DNA repair; DNA-dependent serine/threonine protein kinase (DNA-PK); NHEJ; double-stranded DNA breaks; nucleic acid enzymology; protein structure

Mesh:

Substances:

Year:  2017        PMID: 29247009      PMCID: PMC6036208          DOI: 10.1074/jbc.TM117.000374

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  122 in total

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2.  Autoinhibition of the Nuclease ARTEMIS Is Mediated by a Physical Interaction between Its Catalytic and C-terminal Domains.

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3.  Three-dimensional structure of the human DNA-PKcs/Ku70/Ku80 complex assembled on DNA and its implications for DNA DSB repair.

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Journal:  Mol Cell       Date:  2005-08-05       Impact factor: 17.970

5.  PAXX Is an Accessory c-NHEJ Factor that Associates with Ku70 and Has Overlapping Functions with XLF.

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Journal:  Cell Rep       Date:  2016-10-04       Impact factor: 9.423

6.  PAXX and XLF DNA repair factors are functionally redundant in joining DNA breaks in a G1-arrested progenitor B-cell line.

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Journal:  Nucleic Acids Res       Date:  2012-01-27       Impact factor: 16.971

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