Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair - PubMed (original) (raw)
. 2001 Aug 9;412(6847):607-14.
doi: 10.1038/35088000.
Affiliations
- PMID: 11493912
- DOI: 10.1038/35088000
Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair
J R Walker et al. Nature. 2001.
Abstract
The Ku heterodimer (Ku70 and Ku80 subunits) contributes to genomic integrity through its ability to bind DNA double-strand breaks and facilitate repair by the non-homologous end-joining pathway. The crystal structure of the human Ku heterodimer was determined both alone and bound to a 55-nucleotide DNA element at 2.7 and 2.5 A resolution, respectively. Ku70 and Ku80 share a common topology and form a dyad-symmetrical molecule with a preformed ring that encircles duplex DNA. The binding site can cradle two full turns of DNA while encircling only the central 3-4 base pairs (bp). Ku makes no contacts with DNA bases and few with the sugar-phosphate backbone, but it fits sterically to major and minor groove contours so as to position the DNA helix in a defined path through the protein ring. These features seem well designed to structurally support broken DNA ends and to bring the DNA helix into phase across the junction during end processing and ligation.
Similar articles
- Photocross-linking of an oriented DNA repair complex. Ku bound at a single DNA end.
Yoo S, Kimzey A, Dynan WS. Yoo S, et al. J Biol Chem. 1999 Jul 9;274(28):20034-9. doi: 10.1074/jbc.274.28.20034. J Biol Chem. 1999. PMID: 10391954 - DNA repair: how Ku makes ends meet.
Doherty AJ, Jackson SP. Doherty AJ, et al. Curr Biol. 2001 Nov 13;11(22):R920-4. doi: 10.1016/s0960-9822(01)00555-3. Curr Biol. 2001. PMID: 11719239 Review. - The three-dimensional structure of the C-terminal DNA-binding domain of human Ku70.
Zhang Z, Zhu L, Lin D, Chen F, Chen DJ, Chen Y. Zhang Z, et al. J Biol Chem. 2001 Oct 12;276(41):38231-6. doi: 10.1074/jbc.M105238200. Epub 2001 Jul 16. J Biol Chem. 2001. PMID: 11457852 - Three-dimensional structure of the human DNA-PKcs/Ku70/Ku80 complex assembled on DNA and its implications for DNA DSB repair.
Spagnolo L, Rivera-Calzada A, Pearl LH, Llorca O. Spagnolo L, et al. Mol Cell. 2006 May 19;22(4):511-9. doi: 10.1016/j.molcel.2006.04.013. Mol Cell. 2006. PMID: 16713581 - A Ku bridge over broken DNA.
Jones JM, Gellert M, Yang W. Jones JM, et al. Structure. 2001 Oct;9(10):881-4. doi: 10.1016/s0969-2126(01)00658-x. Structure. 2001. PMID: 11591342 Review.
Cited by
- Identification of the main barriers to Ku accumulation in chromatin.
Bossaert M, Moreno A, Peixoto A, Pillaire MJ, Chanut P, Frit P, Calsou P, Loparo JJ, Britton S. Bossaert M, et al. bioRxiv [Preprint]. 2024 Jan 4:2024.01.03.574002. doi: 10.1101/2024.01.03.574002. bioRxiv. 2024. PMID: 38260538 Free PMC article. Updated. Preprint. - Frequency and genetic characterization of V(DD)J recombinants in the human peripheral blood antibody repertoire.
Briney BS, Willis JR, Hicar MD, Thomas JW 2nd, Crowe JE Jr. Briney BS, et al. Immunology. 2012 Sep;137(1):56-64. doi: 10.1111/j.1365-2567.2012.03605.x. Immunology. 2012. PMID: 22612413 Free PMC article. - Roles for the DNA-PK complex and 53BP1 in protecting ends from resection during DNA double-strand break repair.
Shibata A, Jeggo PA. Shibata A, et al. J Radiat Res. 2020 Sep 8;61(5):718-726. doi: 10.1093/jrr/rraa053. J Radiat Res. 2020. PMID: 32779701 Free PMC article. Review. - The Ku-binding motif is a conserved module for recruitment and stimulation of non-homologous end-joining proteins.
Grundy GJ, Rulten SL, Arribas-Bosacoma R, Davidson K, Kozik Z, Oliver AW, Pearl LH, Caldecott KW. Grundy GJ, et al. Nat Commun. 2016 Apr 11;7:11242. doi: 10.1038/ncomms11242. Nat Commun. 2016. PMID: 27063109 Free PMC article. - Interplay between Ku and Replication Protein A in the Restriction of Exo1-mediated DNA Break End Resection.
Krasner DS, Daley JM, Sung P, Niu H. Krasner DS, et al. J Biol Chem. 2015 Jul 24;290(30):18806-16. doi: 10.1074/jbc.M115.660191. Epub 2015 Jun 11. J Biol Chem. 2015. PMID: 26067273 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous