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Myung, Kyungjae
Center for Genomic Integrity
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Smc5-Smc6 mediate DNA double-strand-break repair by promoting sister-chromatid recombination

Author(s)
De Piccoli, GiacomoCortes-Ledesma, FelipeIra, GregoryTorres-Rosell, JordiUhle, StefanFarmer, SarahHwang, Ji-YoungMachin, FelixCeschia, AudreyMcAleenan, AlexandraCordon-Preciado, VioletaClemente-Blanco, AndresVilella-Mitjana, FelipUllal, PranavJarmuz, AdamLeitao, BeatrizBressan, DebraDotiwala, FarokhPapusha, AlmaZhao, XiaolanMyung, KyungjaeHaber, James E.Aguilera, AndresAragon, Luis
Issued Date
2006-09
DOI
10.1038/ncb1466
URI
https://scholarworks.unist.ac.kr/handle/201301/31069
Fulltext
https://www.nature.com/articles/ncb1466
Citation
NATURE CELL BIOLOGY, v.8, no.9, pp.1032 - U118
Abstract
DNA double-strand breaks (DSB) can arise during DNA replication, or after exposure to DNA-damaging agents, and their correct repair is fundamental for cell survival and genomic stability. Here, we show that the Smc5-Smc6 complex is recruited to DSBs de novo to support their repair by homologous recombination between sister chromatids. In addition, we demonstrate that Smc5-Smc6 is necessary to suppress gross chromosomal rearrangements. Our findings show that the Smc5-Smc6 complex is essential for genome stability as it promotes repair of DSBs by error-free sisterchromatid recombination (SCR), thereby suppressing inappropriate non-sister recombination events.
Publisher
NATURE PUBLISHING GROUP
ISSN
1465-7392
Keyword
SACCHAROMYCES-CEREVISIAEYEASTCOHESINREGIONSGENES

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