Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis. - Wikidata - wikimedia - TriplyDB

Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis.

Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis.

http://www.wikidata.org/entity/Q27940287

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Frequent and efficient use of the sister chromatid for DNA double-strand break repair during budding yeast meiosis Controlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formation The RecQ DNA helicases in DNA repair TOPping off meiosis Smc5/6 coordinates formation and resolution of joint molecules with chromosome morphology to ensure meiotic divisions Joint molecule resolution requires the redundant activities of MUS-81 and XPF-1 during Caenorhabditis elegans meiosis Mammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesis Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination.Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast.Yeast axial-element protein, Red1, binds SUMO chains to promote meiotic interhomologue recombination and chromosome synapsis.Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.RecQ helicase, Sgs1, and XPF family endonuclease, Mus81-Mms4, resolve aberrant joint molecules during meiotic recombination.Multiple mechanisms limit meiotic crossovers: TOP3α and two BLM homologs antagonize crossovers in parallel to FANCM BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions Topoisomerase 3alpha and RMI1 suppress somatic crossovers and are essential for resolution of meiotic recombination intermediates in Arabidopsis thaliana FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice Alignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) Protein The multi-replication protein A (RPA) system--a new perspective.Sgs1 and exo1 redundantly inhibit break-induced replication and de novo telomere addition at broken chromosome ends.Non-SMC elements 1 and 3 are required for early embryo and seedling development in Arabidopsis.Trying to avoid your sister.GEN1/Yen1 and the SLX4 complex: Solutions to the problem of Holliday junction resolution.The roles of the Saccharomyces cerevisiae RecQ helicase SGS1 in meiotic genome surveillance.Mammalian BLM helicase is critical for integrating multiple pathways of meiotic recombination Genetic interference: don't stand so close to me.Meiotic recombination intermediates are resolved with minimal crossover formation during return-to-growth, an analogue of the mitotic cell cycle The Smc5-Smc6 complex is required to remove chromosome junctions in meiosis.Crossover invariance determined by partner choice for meiotic DNA break repair.Combined fluorescent and electron microscopic imaging unveils the specific properties of two classes of meiotic crossovers.Absence of SUN-domain protein Slp1 blocks karyogamy and switches meiotic recombination and synapsis from homologs to sister chromatids.Top3-Rmi1 DNA single-strand decatenase is integral to the formation and resolution of meiotic recombination intermediates.Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast.DNA double-strand break repair in Caenorhabditis elegans Bloom DNA helicase facilitates homologous recombination between diverged homologous sequences Smc5/6-Mms21 prevents and eliminates inappropriate recombination intermediates in meiosis.Mus81-mediated DNA cleavage resolves replication forks stalled by topoisomerase I-DNA complexes.AAA-ATPase FIDGETIN-LIKE 1 and Helicase FANCM Antagonize Meiotic Crossovers by Distinct Mechanisms.Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis

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Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis.

http://www.wikidata.org/entity/Q27940287

description

2008 nî lūn-bûn

@nan

2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

@ast

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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type

label

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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prefLabel

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

@ast

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

@en

Mus81/Mms4 endonuclease and Sg ...... ate metabolism during meiosis.

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J.MOLCEL.2008.05.021

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Mus81/Mms4 endonuclease and Sg ...... iate metabolism during meiosis

@en

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Lea Jessop

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Synthesis-dependent strand annealing in meiosis

BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates

Requirement for three novel protein complexes in the absence of the Sgs1 DNA helicase in Saccharomyces cerevisiae

Mus81 functions in the quality control of replication forks at the rDNA and is involved in the maintenance of rDNA repeat number in Saccharomyces cerevisiae

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family

Polo-like kinase Cdc5 promotes chiasmata formation and cosegregation of sister centromeres at meiosis I.

Gametogenesis in yeast is regulated by a transcriptional cascade dependent on Ndt80.

Control of landmark events in meiosis by the CDK Cdc28 and the meiosis-specific kinase Ime2.

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313-323

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2911038

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10.1016/J.MOLCEL.2008.05.021

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3

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31

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Michael Lichten

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2008-08-01T00:00:00Z

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23160642

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18691964

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2584117

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