Histone displacement during nucleotide excision repair

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Standard

Histone displacement during nucleotide excision repair. / Dinant, C.; Bartek, J.; Bekker-Jensen, S.

I: International Journal of Molecular Sciences (Online), Bind 13, Nr. 10, 17.10.2012, s. 13322-13337.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Dinant, C, Bartek, J & Bekker-Jensen, S 2012, 'Histone displacement during nucleotide excision repair', International Journal of Molecular Sciences (Online), bind 13, nr. 10, s. 13322-13337. https://doi.org/10.3390/ijms131013322

APA

Dinant, C., Bartek, J., & Bekker-Jensen, S. (2012). Histone displacement during nucleotide excision repair. International Journal of Molecular Sciences (Online), 13(10), 13322-13337. https://doi.org/10.3390/ijms131013322

Vancouver

Dinant C, Bartek J, Bekker-Jensen S. Histone displacement during nucleotide excision repair. International Journal of Molecular Sciences (Online). 2012 okt. 17;13(10):13322-13337. https://doi.org/10.3390/ijms131013322

Author

Dinant, C. ; Bartek, J. ; Bekker-Jensen, S. / Histone displacement during nucleotide excision repair. I: International Journal of Molecular Sciences (Online). 2012 ; Bind 13, Nr. 10. s. 13322-13337.

Bibtex

@article{7fbe1c1dde9e413c82b47437f3b533bd,
title = "Histone displacement during nucleotide excision repair",
abstract = "Nucleotide excision repair (NER) is an important DNA repair mechanism required for cellular resistance against UV light and toxic chemicals such as those found in tobacco smoke. In living cells, NER efficiently detects and removes DNA lesions within the large nuclear macromolecular complex called chromatin. The condensed nature of chromatin inhibits many DNA metabolizing activities, including NER. In order to promote efficient repair, detection of a lesion not only has to activate the NER pathway but also chromatin remodeling. In general, such remodeling is thought on the one hand to precede NER, thus allowing repair proteins to efficiently access DNA. On the other hand, after completion of the repair, the chromatin must be returned to its previous undamaged state. Chromatin remodeling can refer to three separate but interconnected processes, histone post-translational modifications, insertion of histone variants and histone displacement (including nucleosome sliding). Here we review current knowledge, and speculate about current unknowns, regarding those chromatin remodeling activities that physically displace histones before, during and after NER.",
author = "C. Dinant and J. Bartek and S. Bekker-Jensen",
year = "2012",
month = oct,
day = "17",
doi = "10.3390/ijms131013322",
language = "English",
volume = "13",
pages = "13322--13337",
journal = "International Journal of Molecular Sciences (Online)",
issn = "1661-6596",
publisher = "MDPI AG",
number = "10",

}

RIS

TY - JOUR

T1 - Histone displacement during nucleotide excision repair

AU - Dinant, C.

AU - Bartek, J.

AU - Bekker-Jensen, S.

PY - 2012/10/17

Y1 - 2012/10/17

N2 - Nucleotide excision repair (NER) is an important DNA repair mechanism required for cellular resistance against UV light and toxic chemicals such as those found in tobacco smoke. In living cells, NER efficiently detects and removes DNA lesions within the large nuclear macromolecular complex called chromatin. The condensed nature of chromatin inhibits many DNA metabolizing activities, including NER. In order to promote efficient repair, detection of a lesion not only has to activate the NER pathway but also chromatin remodeling. In general, such remodeling is thought on the one hand to precede NER, thus allowing repair proteins to efficiently access DNA. On the other hand, after completion of the repair, the chromatin must be returned to its previous undamaged state. Chromatin remodeling can refer to three separate but interconnected processes, histone post-translational modifications, insertion of histone variants and histone displacement (including nucleosome sliding). Here we review current knowledge, and speculate about current unknowns, regarding those chromatin remodeling activities that physically displace histones before, during and after NER.

AB - Nucleotide excision repair (NER) is an important DNA repair mechanism required for cellular resistance against UV light and toxic chemicals such as those found in tobacco smoke. In living cells, NER efficiently detects and removes DNA lesions within the large nuclear macromolecular complex called chromatin. The condensed nature of chromatin inhibits many DNA metabolizing activities, including NER. In order to promote efficient repair, detection of a lesion not only has to activate the NER pathway but also chromatin remodeling. In general, such remodeling is thought on the one hand to precede NER, thus allowing repair proteins to efficiently access DNA. On the other hand, after completion of the repair, the chromatin must be returned to its previous undamaged state. Chromatin remodeling can refer to three separate but interconnected processes, histone post-translational modifications, insertion of histone variants and histone displacement (including nucleosome sliding). Here we review current knowledge, and speculate about current unknowns, regarding those chromatin remodeling activities that physically displace histones before, during and after NER.

UR - http://www.scopus.com/inward/record.url?scp=84870669679&partnerID=8YFLogxK

U2 - 10.3390/ijms131013322

DO - 10.3390/ijms131013322

M3 - Journal article

C2 - 23202955

AN - SCOPUS:84870669679

VL - 13

SP - 13322

EP - 13337

JO - International Journal of Molecular Sciences (Online)

JF - International Journal of Molecular Sciences (Online)

SN - 1661-6596

IS - 10

ER -

ID: 46438396