Nap1 stimulates homologous recombination by RAD51 and RAD54 in higher-ordered chromatin containing histone H1

Homologous recombination plays essential roles in mitotic DNA double strand break (DSB) repair and meiotic genetic recombination. In eukaryotes, RAD51 promotes the central homologous-pairing step during homologous recombination, but is not sufficient to overcome the reaction barrier imposed by nucle...

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Veröffentlicht in:Scientific reports 2014-05, Vol.4 (1), p.4863, Article 4863
Hauptverfasser: Machida, Shinichi, Takaku, Motoki, Ikura, Masae, Sun, Jiying, Suzuki, Hidekazu, Kobayashi, Wataru, Kinomura, Aiko, Osakabe, Akihisa, Tachiwana, Hiroaki, Horikoshi, Yasunori, Fukuto, Atsuhiko, Matsuda, Ryo, Ura, Kiyoe, Tashiro, Satoshi, Ikura, Tsuyoshi, Kurumizaka, Hitoshi
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Sprache:eng
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Zusammenfassung:Homologous recombination plays essential roles in mitotic DNA double strand break (DSB) repair and meiotic genetic recombination. In eukaryotes, RAD51 promotes the central homologous-pairing step during homologous recombination, but is not sufficient to overcome the reaction barrier imposed by nucleosomes. RAD54, a member of the ATP-dependent nucleosome remodeling factor family, is required to promote the RAD51-mediated homologous pairing in nucleosomal DNA. In higher eukaryotes, most nucleosomes form higher-ordered chromatin containing the linker histone H1. However, the mechanism by which RAD51/RAD54-mediated homologous pairing occurs in higher-ordered chromatin has not been elucidated. In this study, we found that a histone chaperone, Nap1, accumulates on DSB sites in human cells and DSB repair is substantially decreased in Nap1-knockdown cells. We determined that Nap1 binds to RAD54, enhances the RAD54-mediated nucleosome remodeling by evicting histone H1 and eventually stimulates the RAD51-mediated homologous pairing in higher-ordered chromatin containing histone H1.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep04863