Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase - Test2 - elhamkhani - TriplyDB

Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase

Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase

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Controlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formation Mus81 nuclease and Sgs1 helicase are essential for meiotic recombination in a protist lacking a synaptonemal complex Hold your horSSEs: controlling structure-selective endonucleases MUS81 and Yen1/GEN1 Mechanisms and regulation of mitotic recombination in Saccharomyces cerevisiae TOPping off meiosis Repair of strand breaks by homologous recombination The SMC-5/6 Complex and the HIM-6 (BLM) Helicase Synergistically Promote Meiotic Recombination Intermediate Processing and Chromosome Maturation during Caenorhabditis elegans Meiosis Smc5/6 coordinates formation and resolution of joint molecules with chromosome morphology to ensure meiotic divisions Combinatorial regulation of meiotic holliday junction resolution in C. elegans by HIM-6 (BLM) helicase, SLX-4, and the SLX-1, MUS-81 and XPF-1 nucleases Joint molecule resolution requires the redundant activities of MUS-81 and XPF-1 during Caenorhabditis elegans meiosis SPO11-independent DNA repair foci and their role in meiotic silencing Synaptonemal Complex Proteins of Budding Yeast Define Reciprocal Roles in MutSγ-Mediated Crossover Formation Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast.Complex chromosomal rearrangements mediated by break-induced replication involve structure-selective endonucleases.Budding Yeast SLX4 Contributes to the Appropriate Distribution of Crossovers and Meiotic Double-Strand Break Formation on Bivalents During Meiosis.Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation.New insights into the mechanism of DNA mismatch repair Variation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiae Multiple mechanisms limit meiotic crossovers: TOP3α and two BLM homologs antagonize crossovers in parallel to FANCM Recombination, Pairing, and Synapsis of Homologs during Meiosis Mlh1-Mlh3, a meiotic crossover and DNA mismatch repair factor, is a Msh2-Msh3-stimulated endonuclease The Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions.RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis Interplay between structure-specific endonucleases for crossover control during Caenorhabditis elegans meiosis Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway Evidence of a Mild Mutator Phenotype in Cambodian Plasmodium falciparum Malaria Parasites DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae Mechanisms for Structural Variation in the Human Genome The mismatch repair and meiotic recombination endonuclease Mlh1-Mlh3 is activated by polymer formation and can cleave DNA substrates in trans.Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis.The Mus81-Mms4 structure-selective endonuclease requires nicked DNA junctions to undergo conformational changes and bend its DNA substrates for cleavage.Crossover recombination mediated by HIM-18/SLX4-associated nucleases.Combined fluorescent and electron microscopic imaging unveils the specific properties of two classes of meiotic crossovers.DNA helicase HIM-6/BLM both promotes MutSγ-dependent crossovers and antagonizes MutSγ-independent interhomolog associations during caenorhabditis elegans meiosis.Top3-Rmi1 DNA single-strand decatenase is integral to the formation and resolution of meiotic recombination intermediates.Msh4 and Msh5 function in SC-independent chiasma formation during the streamlined meiosis of Tetrahymena Trinucleotide expansion in disease: why is there a length threshold?Heteroduplex DNA position defines the roles of the Sgs1, Srs2, and Mph1 helicases in promoting distinct recombination outcomes.Synthetic lethality between gene defects affecting a single non-essential molecular pathway with reversible steps.An elegans Solution for Crossover Formation.

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Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase

http://www.wikidata.org/entity/Q28264475

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2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Delineation of joint molecule ...... a crossover-specific resolvase

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Kseniya Zakharyevich

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Neil Hunter

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Shangming Tang

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Yunmei Ma

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P2860

Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair

Drosophila MUS312 and the vertebrate ortholog BTBD12 interact with DNA structure-specific endonucleases in DNA repair and recombination

Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair

MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice

PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair

A tale of tails: insights into the coordination of 3' end processing during homologous recombination

RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability

BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

The Bloom's syndrome gene product promotes branch migration of holliday junctions

Caenorhabditis elegans HIM-18/SLX-4 interacts with SLX-1 and XPF-1 and maintains genomic integrity in the germline by processing recombination intermediates

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10.1016/J.CELL.2012.03.023

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22500800

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