Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover. - Wikidata - awgldk - TriplyDB

Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

http://www.wikidata.org/entity/Q41445085

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Cdk1 targets Srs2 to complete synthesis-dependent strand annealing and to promote recombinational repair The RecQ DNA helicases in DNA repair Meiotic versus mitotic recombination: two different routes for double-strand break repair: the different functions of meiotic versus mitotic DSB repair are reflected in different pathway usage and different outcomes Comparative genomics and molecular dynamics of DNA repeats in eukaryotes Mechanisms and regulation of mitotic recombination in Saccharomyces cerevisiae Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination.Nej1 recruits the Srs2 helicase to DNA double-strand breaks and supports repair by a single-strand annealing-like mechanism.Interplay between the Smc5/6 complex and the Mph1 helicase in recombinational repair Srs2 mediates PCNA-SUMO-dependent inhibition of DNA repair synthesis.Mrc1 and Tof1 regulate DNA replication forks in different ways during normal S phase Esc2 and Sgs1 act in functionally distinct branches of the homologous recombination repair pathway in Saccharomyces cerevisiae.Srs2 promotes Mus81-Mms4-mediated resolution of recombination intermediates.Rad52 sumoylation prevents the toxicity of unproductive Rad51 filaments independently of the anti-recombinase Srs2 Elevated histone expression promotes life span extension Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1.Srs2 promotes synthesis-dependent strand annealing by disrupting DNA polymerase δ-extending D-loops Distinct Cdk1 requirements during single-strand annealing, noncrossover, and crossover recombination.Visualization of recombination-mediated damage bypass by template switching.The chromatin assembly factor 1 promotes Rad51-dependent template switches at replication forks by counteracting D-loop disassembly by the RecQ-type helicase Rqh1 Unwinding of synthetic replication and recombination substrates by Srs2.Continued DNA synthesis in replication checkpoint mutants leads to fork collapse.Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast.Heteroduplex DNA position defines the roles of the Sgs1, Srs2, and Mph1 helicases in promoting distinct recombination outcomes.Srs2 overexpression reveals a helicase-independent role at replication forks that requires diverse cell functions Top3-Rmi1 dissolve Rad51-mediated D loops by a topoisomerase-based mechanism.Multiple regulation of Rad51-mediated homologous recombination by fission yeast Fbh1.SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination.Mechanism of DNA damage tolerance.Srs2 and Mus81-Mms4 Prevent Accumulation of Toxic Inter-Homolog Recombination Intermediates.Local regulation of the Srs2 helicase by the SUMO-like domain protein Esc2 promotes recombination at sites of stalled replication.The human F-Box DNA helicase FBH1 faces Saccharomyces cerevisiae Srs2 and postreplication repair pathway roles.Sequence divergence impedes crossover more than noncrossover events during mitotic gap repair in yeast.Srs2 removes deadly recombination intermediates independently of its interaction with SUMO-modified PCNA Rad51 gain-of-function mutants that exhibit high affinity DNA binding cause DNA damage sensitivity in the absence of Srs2.Break-induced replication occurs by conservative DNA synthesis The Saccharomyces cerevisiae Esc2 and Smc5-6 proteins promote sister chromatid junction-mediated intra-S repair.Suppression of the double-strand-break-repair defect of the Saccharomyces cerevisiae rad57 mutant MRE11 complex links RECQ5 helicase to sites of DNA damage.Resolution by unassisted Top3 points to template switch recombination intermediates during DNA replication.Readers of PCNA modifications

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Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

http://www.wikidata.org/entity/Q41445085

description

2006 nî lūn-bûn

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2006年の論文

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2006年论文

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2006年论文

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Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

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Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

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Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

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SJ.EMBOJ.7601158

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The EMBO Journal

P1476

Mrc1 and Srs2 are major actors in the regulation of spontaneous crossover.

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P2093

Delphine Dervins

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Francis Fabre

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Serge Gangloff

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Thomas Robert

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P2860

Cellular roles of dna topoisomerases: a molecular perspective

Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae

BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures

Direct DNA binding by Brca1

A comprehensive two-hybrid analysis to explore the yeast protein interactome

Molecular anatomy and regulation of a stable replisome at a paused eukaryotic DNA replication fork.

The Srs2 helicase prevents recombination by disrupting Rad51 nucleoprotein filaments.

A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiae

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

Mrc1 and Tof1 promote replication fork progression and recovery independently of Rad53.

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2837-2846

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10.1038/SJ.EMBOJ.7601158

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25

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2006-05-25T00:00:00Z

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16724109

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