The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism (Q79120277)

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19 December 2019

title

The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism (English)

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19 December 2019

author

Pierre-Henri L Gaillard

1

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19 December 2019

Eishi Noguchi

2

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19 December 2019

author name string

Paul Shanahan

3

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19 December 2019

Paul Russell

4

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19 December 2019

publication date

1 September 2003

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19 December 2019

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19 December 2019

volume

12

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19 December 2019

issue

3

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19 December 2019

page(s)

747-759

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Differential timing and control of noncrossover and crossover recombination during meiosis

19 December 2019

cites work

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The Mechanism of Mus81-Mms4 Cleavage Site Selection Distinguishes It from the Homologous Endonuclease Rad1-Rad10

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Mus81-Eme1 are essential components of a Holliday junction resolvase

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Yeast Resolving Enzyme CCE1 Makes Sequential Cleavages in DNA Junctions within the Lifetime of the Complex†

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Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair

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Near-simultaneous DNA cleavage by the subunits of the junction-resolving enzyme T4 endonuclease VII.

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The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination

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MUS81 encodes a novel helix-hairpin-helix protein involved in the response to UV- and methylation-induced DNA damage in Saccharomyces cerevisiae

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Functional overlap between Sgs1-Top3 and the Mms4-Mus81 endonuclease

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Repair of an interstrand DNA cross-link initiated by ERCC1-XPF repair/recombination nuclease.

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7 January 2021

Generating crossovers by resolution of nicked Holliday junctions: a role for Mus81-Eme1 in meiosis

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7 January 2021

Identification of double Holliday junctions as intermediates in meiotic recombination.

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7 January 2021

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7 January 2021

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7 January 2021

The RuvC protein dimer resolves Holliday junctions by a dual incision mechanism that involves base-specific contacts

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7 January 2021

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Holliday junctions accumulate in replication mutants via a RecA homolog-independent mechanism

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14527419 AND SRC:MED&resulttype=core&format=json

19 December 2019

1 reference