| Literature DB >> 27720644 |
Muwen Kong1, Lili Liu1, Xuejing Chen2, Katherine I Driscoll3, Peng Mao4, Stefanie Böhm5, Neil M Kad6, Simon C Watkins7, Kara A Bernstein5, John J Wyrick4, Jung-Hyun Min8, Bennett Van Houten9.
Abstract
Nucleotide excision repair (NER) is an evolutionarily conserved mechanism that processes helix-destabilizing and/or -distorting DNA lesions, such as UV-induced photoproducts. Here, we investigate the dynamic protein-DNA interactions during the damage recognition step using single-molecule fluorescence microscopy. Quantum dot-labeled Rad4-Rad23 (yeast XPC-RAD23B ortholog) forms non-motile complexes or conducts a one-dimensional search via either random diffusion or constrained motion. Atomic force microcopy analysis of Rad4 with the β-hairpin domain 3 (BHD3) deleted reveals that this motif is non-essential for damage-specific binding and DNA bending. Furthermore, we find that deletion of seven residues in the tip of β-hairpin in BHD3 increases Rad4-Rad23 constrained motion at the expense of stable binding at sites of DNA lesions, without diminishing cellular UV resistance or photoproduct repair in vivo. These results suggest a distinct intermediate in the damage recognition process during NER, allowing dynamic DNA damage detection at a distance.Entities:
Keywords: DNA tightrope assay; Rad23; Rad4; XPC; dynamic DNA damage recognition; nucleotide excision repair; quantum dots; single particle tracking; xeroderma pigmentosum
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Year: 2016 PMID: 27720644 PMCID: PMC5123691 DOI: 10.1016/j.molcel.2016.09.005
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970