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DNA activates the Nse2/Mms21 SUMO E3 ligase in the Smc5/6 complex.
- Source :
-
The EMBO journal [EMBO J] 2018 Jun 15; Vol. 37 (12). Date of Electronic Publication: 2018 May 16. - Publication Year :
- 2018
-
Abstract
- Modification of chromosomal proteins by conjugation to SUMO is a key step to cope with DNA damage and to maintain the integrity of the genome. The recruitment of SUMO E3 ligases to chromatin may represent one layer of control on protein sumoylation. However, we currently do not understand how cells upregulate the activity of E3 ligases on chromatin. Here we show that the Nse2 SUMO E3 in the Smc5/6 complex, a critical player during recombinational DNA repair, is directly stimulated by binding to DNA Activation of sumoylation requires the electrostatic interaction between DNA and a positively charged patch in the ARM domain of Smc5, which acts as a DNA sensor that subsequently promotes a stimulatory activation of the E3 activity in Nse2. Specific disruption of the interaction between the ARM of Smc5 and DNA sensitizes cells to DNA damage, indicating that this mechanism contributes to DNA repair. These results reveal a mechanism to enhance a SUMO E3 ligase activity by direct DNA binding and to restrict sumoylation in the vicinity of those Smc5/6-Nse2 molecules engaged on DNA.<br /> (© 2018 The Authors.)
- Subjects :
- Cell Cycle Proteins genetics
Cell Cycle Proteins metabolism
DNA Damage
DNA, Fungal genetics
DNA, Fungal metabolism
Enzyme Activation
Multiprotein Complexes genetics
Multiprotein Complexes metabolism
SUMO-1 Protein genetics
SUMO-1 Protein metabolism
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins genetics
Saccharomyces cerevisiae Proteins metabolism
Sumoylation
Ubiquitin-Protein Ligases genetics
Ubiquitin-Protein Ligases metabolism
Cell Cycle Proteins chemistry
DNA, Fungal chemistry
Multiprotein Complexes chemistry
SUMO-1 Protein chemistry
Saccharomyces cerevisiae chemistry
Saccharomyces cerevisiae Proteins chemistry
Ubiquitin-Protein Ligases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2075
- Volume :
- 37
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- The EMBO journal
- Publication Type :
- Academic Journal
- Accession number :
- 29769404
- Full Text :
- https://doi.org/10.15252/embj.201798306