Interactome analysis identifies a new paralogue of XRCC4 in non-homologous end joining DNA repair pathway-Reference-Cited by-同舟云学术

Interactome analysis identifies a new paralogue of XRCC4 in non-homologous end joining DNA repair pathway

Published:2015-02-11 Issue:1 Volume:6 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Xing Mengtan,Yang Mingrui,Huo Wei,Feng Feng,Wei Leizhen,Jiang Wenxia,Ning Shaokai,Yan Zhenxin,Li Wen,Wang Qingsong,Hou Mei,Dong Chunxia,Guo Rong,Gao Ge,Ji Jianguo,Zha Shan,Lan Li,Liang Huanhuan,Xu Dongyi^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms7233.pdf

Reference40 articles.

1. Waters, C. A., Strande, N. T., Wyatt, D. W., Pryor, J. M. & Ramsden, D. A. Nonhomologous end joining: a good solution for bad ends. DNA Repair (Amst) 17, 39–51 (2014).

2. Lieber, M. R. The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway. Annu. Rev. Biochem. 79, 181–211 (2010).

3. Mahaney, B. L., Hammel, M., Meek, K., Tainer, J. A. & Lees-Miller, S. P. XRCC4 and XLF form long helical protein filaments suitable for DNA end protection and alignment to facilitate DNA double strand break repair. Biochem. Cell Biol. 91, 31–41 (2013).

4. van Breugel, M. et al. Structures of SAS-6 suggest its organization in centrioles. Science 331, 1196–1199 (2011).

5. Kitagawa, D. et al. Structural basis of the 9-fold symmetry of centrioles. Cell 144, 364–375 (2011).

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