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SUMOylation of Rad52-Rad59 synergistically change the outcome of mitotic recombination

S. Silva, V. Altmannova, N. Eckert-Boulet, P. Kolesar, I. Gallina, L. Hang, I. Chung, M. Arneric, X. Zhao, LD. Buron, UH. Mortensen, L. Krejci, M. Lisby,

. 2016 ; 42 (-) : 11-25. [pub] 20160416

Language English Country Netherlands

Document type Journal Article

Persistent link   https://www.medvik.cz/link/bmc17024028

Homologous recombination (HR) is essential for maintenance of genome stability through double-strand break (DSB) repair, but at the same time HR can lead to loss of heterozygosity and uncontrolled recombination can be genotoxic. The post-translational modification by SUMO (small ubiquitin-like modifier) has been shown to modulate recombination, but the exact mechanism of this regulation remains unclear. Here we show that SUMOylation stabilizes the interaction between the recombination mediator Rad52 and its paralogue Rad59 in Saccharomyces cerevisiae. Although Rad59 SUMOylation is not required for survival after genotoxic stress, it affects the outcome of recombination to promote conservative DNA repair. In some genetic assays, Rad52 and Rad59 SUMOylation act synergistically. Collectively, our data indicate that the described SUMO modifications affect the balance between conservative and non-conservative mechanisms of HR.

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$a Homologous recombination (HR) is essential for maintenance of genome stability through double-strand break (DSB) repair, but at the same time HR can lead to loss of heterozygosity and uncontrolled recombination can be genotoxic. The post-translational modification by SUMO (small ubiquitin-like modifier) has been shown to modulate recombination, but the exact mechanism of this regulation remains unclear. Here we show that SUMOylation stabilizes the interaction between the recombination mediator Rad52 and its paralogue Rad59 in Saccharomyces cerevisiae. Although Rad59 SUMOylation is not required for survival after genotoxic stress, it affects the outcome of recombination to promote conservative DNA repair. In some genetic assays, Rad52 and Rad59 SUMOylation act synergistically. Collectively, our data indicate that the described SUMO modifications affect the balance between conservative and non-conservative mechanisms of HR.
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$a Altmannová, Veronika $u Department of Biology, Masaryk University, Kamenice 5/A7, 62500 Brno, Czech Republic. $7 mub2011626283
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$a Eckert-Boulet, Nadine $u Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen N, Denmark.
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$a Kolesar, Peter $u Department of Biology, Masaryk University, Kamenice 5/A7, 62500 Brno, Czech Republic.
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$a Gallina, Irene $u Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen N, Denmark.
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$a Hang, Lisa $u Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
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$a Chung, Inn $u Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
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$a Arneric, Milica $u Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA. $7 gn_A_00008679
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$a Zhao, Xiaolan $u Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
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$a Buron, Line Due $u Department of Systems Biology, Technical University of Denmark, Building 223, 2800 Kgs. Lyngby, Denmark.
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$a Mortensen, Uffe H $u Department of Systems Biology, Technical University of Denmark, Building 223, 2800 Kgs. Lyngby, Denmark.
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$a Krejci, Lumir $u Department of Biology, Masaryk University, Kamenice 5/A7, 62500 Brno, Czech Republic; National Centre for Biomolecular Research, Masaryk University, Kamenice 5/A4, Brno 625 00, Czech Republic; International Clinical Research Center, Center for Biomolecular and Cellular Engineering, St. Anne's University Hospital Brno, Brno, Czech Republic.
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$a Lisby, Michael $u Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen N, Denmark. Electronic address: mlisby@bio.ku.dk.
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