Local regulation of the Srs2 helicase by the SUMO-like domain protein Esc2 promotes recombination at sites of stalled replication
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F15%3A00063388" target="_blank" >RIV/00159816:_____/15:00063388 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/15:00081195
Result on the web
<a href="http://dx.doi.org/10.1101/gad.265629.115" target="_blank" >http://dx.doi.org/10.1101/gad.265629.115</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1101/gad.265629.115" target="_blank" >10.1101/gad.265629.115</a>
Alternative languages
Result language
angličtina
Original language name
Local regulation of the Srs2 helicase by the SUMO-like domain protein Esc2 promotes recombination at sites of stalled replication
Original language description
Accurate completion of replication relies on the ability of cells to activate error-free recombination-mediated DNA damage bypass at sites of perturbed replication. However, as anti-recombinase activities are also recruited to replication forks, how recombination-mediated damage bypass is enabled at replication stress sites remained puzzling. Here we uncovered that the conserved SUMO-like domain-containing Saccharomyces cerevisiae protein Esc2 facilitates recombination-mediated DNA damage tolerance by allowing optimal recruitment of the Rad51 recombinase specifically at sites of perturbed replication. Mechanistically, Esc2 binds stalled replication forks and counteracts the anti-recombinase Srs2 helicase via a two-faceted mechanism involving chromatinrecruitment and turnover of Srs2. Importantly, point mutations in the SUMO-like domains of Esc2 that reduce its interaction with Srs2 cause suboptimal levels of Rad51 recruitment at damaged replication forks. In conclusion, our results re
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Genes & Development
ISSN
0890-9369
e-ISSN
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Volume of the periodical
29
Issue of the periodical within the volume
19
Country of publishing house
US - UNITED STATES
Number of pages
14
Pages from-to
2067-2080
UT code for WoS article
000363002700009
EID of the result in the Scopus database
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