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dc.contributor.author
Bittmann, Julia
dc.contributor.author
Grigaitis, Rokas
dc.contributor.author
Galanti, Lorenzo
dc.contributor.author
Amarell, Silas
dc.contributor.author
Wilfling, Florian
dc.contributor.author
Matos, Joao
dc.contributor.author
Pfander, Boris
dc.date.accessioned
2020-09-14T09:52:29Z
dc.date.available
2020-05-07T07:03:06Z
dc.date.available
2020-05-08T09:31:35Z
dc.date.available
2020-09-14T09:52:29Z
dc.date.issued
2020-04-30
dc.identifier.issn
2050-084X
dc.identifier.other
10.7554/elife.52459
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/413478
dc.identifier.doi
10.3929/ethz-b-000413478
dc.description.abstract
Cell cycle tags allow to restrict target protein expression to specific cell cycle phases. Here, we present an advanced toolbox of cell cycle tag constructs in budding yeast with defined and compatible peak expression that allow comparison of protein functionality at different cell cycle phases. We apply this technology to the question of how and when Mus81-Mms4 and Yen1 nucleases act on DNA replication or recombination structures. Restriction of Mus81-Mms4 to M phase but not S phase allows a wildtype response to various forms of replication perturbation and DNA damage in S phase, suggesting it acts as a post-replicative resolvase. Moreover, we use cell cycle tags to reinstall cell cycle control to a deregulated version of Yen1, showing that its premature activation interferes with the response to perturbed replication. Curbing resolvase activity and establishing a hierarchy of resolution mechanisms are therefore the principal reasons underlying resolvase cell cycle regulation.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
eLife Sciences Publications
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Cell cycle
en_US
dc.subject
Homologous recombination
en_US
dc.subject
Joint molecule resolution
en_US
dc.subject
Post-translational modification
en_US
dc.subject
Genome stability
en_US
dc.title
An advanced cell cycle tag toolbox reveals principles underlying temporal control of structure-selective nucleases
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2020-04-30
ethz.journal.title
eLife
ethz.journal.volume
9
en_US
ethz.pages.start
e52459
en_US
ethz.size
29 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Cambridge
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02517 - Institut für Biochemie / Institute of Biochemistry (IBC)::09457 - Matos, Joao (ehemalig) / Matos, Joao (former)
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02517 - Institut für Biochemie / Institute of Biochemistry (IBC)::09457 - Matos, Joao (ehemalig) / Matos, Joao (former)
en_US
ethz.date.deposited
2020-05-07T07:03:14Z
ethz.source
FORM
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2020-09-14T09:52:43Z
ethz.rosetta.lastUpdated
2022-03-29T03:07:39Z
ethz.rosetta.versionExported
true
ethz.COinS
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