Journal article
Accessing DNA damage in chromatin: Preparing the chromatin landscape for base excision repair
DNA repair, Vol.32, pp.113-119
08/2015
Handle:
https://hdl.handle.net/2376/115226
PMCID: PMC4522338
PMID: 25957487
Abstract
DNA damage in chromatin comes in many forms, including single base lesions that induce base excision repair (BER). We and others have shown that the structural location of DNA lesions within nucleosomes greatly influences their accessibility to repair enzymes. Indeed, a difference in the location of uracil as small as one-half turn of the DNA backbone on the histone surface can result in a 10-fold difference in the time course of its removal in vitro. In addition, the cell has evolved several interdependent processes capable of enhancing the accessibility of excision repair enzymes to DNA lesions in nucleosomes, including post-translational modification of histones, ATP-dependent chromatin remodeling and interchange of histone variants in nucleosomes. In this review, we focus on different factors that affect accessibility of BER enzymes to nucleosomal DNA.
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Details
- Title
- Accessing DNA damage in chromatin: Preparing the chromatin landscape for base excision repair
- Creators
- Yesenia Rodriguez - School of Molecular Biosciences, Washington State University, Pullman, WA 99164-7520, United StatesJohn M Hinz - School of Molecular Biosciences, Washington State University, Pullman, WA 99164-7520, United StatesMichael J Smerdon - School of Molecular Biosciences, Washington State University, Pullman, WA 99164-7520, United States. Electronic address: smerdon@vetmed.wsu.edu
- Publication Details
- DNA repair, Vol.32, pp.113-119
- Academic Unit
- Molecular Biosciences, School of
- Publisher
- Netherlands
- Grant note
- R37 ES002614 / NIEHS NIH HHS R01 ES002614 / NIEHS NIH HHS ES002614 / NIEHS NIH HHS T32 GM008336 / NIGMS NIH HHS R01 ES004106 / NIEHS NIH HHS ES004106 / NIEHS NIH HHS R21 ES020955 / NIEHS NIH HHS ES020955 / NIEHS NIH HHS
- Identifiers
- 99900547569701842
- Language
- English
- Resource Type
- Journal article