Literature DB >> 14697755

High G/C content of cohesive overhangs renders DNA end joining Ku-independent.

Ana Sandoval1, Paul Labhart.   

Abstract

Ku plays an important role in the repair of double strand DNA breaks by non-homologous DNA end joining (NHEJ). Ku is thought to exert its function by aligning the two DNA ends. A previous study showed that the joining of certain cohesive DNA ends in cell-free in vitro reactions was independent of Ku [Mol. Cell. Biol. 19 (1999) 2585]. To investigate a possible correlation between Ku-dependence of DNA end joining reactions and the strength of base pair interactions between cohesive ends, we constructed a series of repair substrates with either 3'- or 5'-overhangs, which consisted entirely of either A/T or G/C residues. We found that after Ku-immunodepletion of the extract, the joining of cohesive ends that associate by the formation of four A:T base pairs was reduced, while the joining of ends that associate through four G:C base pairs was unaffected or slightly stimulated. The precision of the repair was not reduced in Ku-independent reactions. Our results indicate that the requirement for Ku is dependent on how stably the two cohesive DNA ends can associate by base-pairing. Two independent assays for protein-DNA interactions did not reveal any differences in Ku binding to substrates with A/T and G/C overhangs, suggesting that in this system Ku is recruited to the repair site regardless of whether it is functionally required or not. The finding that Ku is dispensable for efficient and precise joining of ends with cohesive G/C overhangs also suggests that alignment of DNA ends may be the sole function of Ku during NHEJ.

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Year:  2004        PMID: 14697755     DOI: 10.1016/j.dnarep.2003.08.014

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  7 in total

1.  Rejoining of DNA double-strand breaks as a function of overhang length.

Authors:  James M Daley; Thomas E Wilson
Journal:  Mol Cell Biol       Date:  2005-02       Impact factor: 4.272

2.  Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions.

Authors:  Amy Marie Yu; Mitch McVey
Journal:  Nucleic Acids Res       Date:  2010-05-11       Impact factor: 19.160

3.  Zinc-finger nuclease-driven targeted integration into mammalian genomes using donors with limited chromosomal homology.

Authors:  Salvatore J Orlando; Yolanda Santiago; Russell C DeKelver; Yevgeniy Freyvert; Elizabeth A Boydston; Erica A Moehle; Vivian M Choi; Sunita M Gopalan; Jacqueline F Lou; James Li; Jeffrey C Miller; Michael C Holmes; Philip D Gregory; Fyodor D Urnov; Gregory J Cost
Journal:  Nucleic Acids Res       Date:  2010-06-08       Impact factor: 16.971

4.  The human set and transposase domain protein Metnase interacts with DNA Ligase IV and enhances the efficiency and accuracy of non-homologous end-joining.

Authors:  Robert Hromas; Justin Wray; Suk-Hee Lee; Leah Martinez; Jacqueline Farrington; Lori Kwan Corwin; Heather Ramsey; Jac A Nickoloff; Elizabeth A Williamson
Journal:  DNA Repair (Amst)       Date:  2008-09-18

5.  Capture of linear fragments at a double-strand break in yeast.

Authors:  Anat Haviv-Chesner; Yoshifumi Kobayashi; Abram Gabriel; Martin Kupiec
Journal:  Nucleic Acids Res       Date:  2007-08-01       Impact factor: 16.971

6.  Linking high GC content to the repair of double strand breaks in prokaryotic genomes.

Authors:  J L Weissman; William F Fagan; Philip L F Johnson
Journal:  PLoS Genet       Date:  2019-11-08       Impact factor: 6.020

7.  Ku heterodimer-independent end joining in Trypanosoma brucei cell extracts relies upon sequence microhomology.

Authors:  Peter Burton; David J McBride; Jonathan M Wilkes; J David Barry; Richard McCulloch
Journal:  Eukaryot Cell       Date:  2007-08-10
  7 in total

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