Sumoylation regulates the stability and nuclease activity of Saccharomyces cerevisiae Dna2

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作者
Lepakshi Ranjha
Maryna Levikova
Veronika Altmannova
Lumir Krejci
Petr Cejka
机构
[1] Università della Svizzera italiana (USI),Institute for Research in Biomedicine
[2] Faculty of Biomedical Sciences,Institute of Molecular Cancer Research
[3] University of Zürich,Department of Biology
[4] Masaryk University,International Clinical Research Center
[5] St. Anne’s University Hospital,National Center for Biomolecular Research
[6] Masaryk University,Department of Biology, Institute of Biochemistry
[7] Eidgenössische Technische Hochschule (ETH),undefined
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Communications Biology | / 2卷
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摘要
Dna2 is an essential nuclease-helicase that acts in several distinct DNA metabolic pathways including DNA replication and recombination. To balance these functions and prevent unscheduled DNA degradation, Dna2 activities must be regulated. Here we show that Saccharomyces cerevisiae Dna2 function is controlled by sumoylation. We map the sumoylation sites to the N-terminal regulatory domain of Dna2 and show that in vitro sumoylation of recombinant Dna2 impairs its nuclease but not helicase activity. In cells, the total levels of the non-sumoylatable Dna2 variant are elevated. However, non-sumoylatable Dna2 shows impaired nuclear localization and reduced recruitment to foci upon DNA damage. Non-sumoylatable Dna2 reduces the rate of DNA end resection, as well as impedes cell growth and cell cycle progression through S phase. Taken together, these findings show that in addition to Dna2 phosphorylation described previously, Dna2 sumoylation is required for the homeostasis of the Dna2 protein function to promote genome stability.
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[1]  
Jackson SP(2013)Regulation of DNA damage responses by ubiquitin and SUMO Mol. Cell 49 795-807
[2]  
Durocher D(2013)Control of nuclear activities by substrate-selective and protein-group SUMOylation Annu. Rev. Genet. 47 167-186
[3]  
Jentsch S(2014)Two-way communications between ubiquitin-like modifiers and DNA Nat. Struct. Mol. Biol. 21 317-324
[4]  
Psakhye I(2012)SUMO wrestles with recombination Biomolecules 2 350-375
[5]  
Ulrich HD(2009)Principles of ubiquitin and SUMO modifications in DNA repair Nature 458 461-467
[6]  
Altmannova V(2016)Ubiquitin-dependent and independent roles of SUMO in proteostasis Am. J. Physiol. Cell Physiol. 311 C284-C296
[7]  
Kolesar P(2015)SUMO-mediated regulation of DNA damage repair and responses Trends Biochem. Sci. 40 233-242
[8]  
Krejci L(2007)SUMO junction-what’s your function? New insights through SUMO-interacting motifs EMBO Rep. 8 550-555
[9]  
Bergink S(2012)Protein group modification and synergy in the SUMO pathway as exemplified in DNA repair Cell 151 807-820
[10]  
Jentsch S(2000)The nuclease activity of the yeast DNA2 protein, which is related to the RecB-like nucleases, is essential in vivo J. Biol. Chem. 275 16518-16529