Int. J. Mol. Sci. 2013, 14(2), 2355-2369; doi:10.3390/ijms14022355

Connecting Chromatin Modifying Factors to DNA Damage Response

1,2,3email, 1,2,3email, 4,5,* email and 1,2,3,* email
Received: 24 September 2012; in revised form: 11 December 2012 / Accepted: 9 January 2013 / Published: 24 January 2013
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Cells are constantly damaged by factors that can induce DNA damage. Eukaryotic cells must rapidly load DNA repair proteins onto damaged chromatin during the DNA damage response (DDR). Chromatin-remodeling complexes use the energy from ATP hydrolysis to remodel nucleosomes and have well-established functions in transcription. Emerging lines of evidence indicate that chromatin-remodeling complexes are important and may remodel nucleosomes during DNA damage repair. New studies also reveal that ATP-dependent chromatin remodeling is involved in cell cycle progression, signal transduction pathways, and interaction and modification of DDR-related proteins that are specifically and intimately connected with the process of DNA damage. This article summarizes the recent advances in our understanding of the interplay between chromatin remodeling and DNA damage response.
Keywords: chromatin-remodeling factor; DNA damage response; signaling transduction pathway; cell cycle; protein interaction; protein modification; double strand breaks
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MDPI and ACS Style

Lai, W.; Li, H.; Liu, S.; Tao, Y. Connecting Chromatin Modifying Factors to DNA Damage Response. Int. J. Mol. Sci. 2013, 14, 2355-2369.

AMA Style

Lai W, Li H, Liu S, Tao Y. Connecting Chromatin Modifying Factors to DNA Damage Response. International Journal of Molecular Sciences. 2013; 14(2):2355-2369.

Chicago/Turabian Style

Lai, Weiwei; Li, Hongde; Liu, Shuang; Tao, Yongguang. 2013. "Connecting Chromatin Modifying Factors to DNA Damage Response." Int. J. Mol. Sci. 14, no. 2: 2355-2369.

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