Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
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Frequent and efficient use of the sister chromatid for DNA double-strand break repair during budding yeast meiosisControlling meiotic recombinational repair - specifying the roles of ZMMs, Sgs1 and Mus81/Mms4 in crossover formationPolo-like kinase is required for synaptonemal complex disassembly and phosphorylation in mouse spermatocytesThe Sum1/Ndt80 transcriptional switch and commitment to meiosis in Saccharomyces cerevisiaePositive feedback of NDT80 expression ensures irreversible meiotic commitment in budding yeastSmc5/6 coordinates formation and resolution of joint molecules with chromosome morphology to ensure meiotic divisionsDot1-dependent histone H3K79 methylation promotes activation of the Mek1 meiotic checkpoint effector kinase by regulating the Hop1 adaptorIpl1/Aurora kinase suppresses S-CDK-driven spindle formation during prophase I to ensure chromosome integrity during meiosisThe Ime2 protein kinase enhances the disassociation of the Sum1 repressor from middle meiotic promoters.Ndj1, a telomere-associated protein, regulates centrosome separation in budding yeast meiosis.Mek1 Down Regulates Rad51 Activity during Yeast Meiosis by Phosphorylation of Hed1Condensin suppresses recombination and regulates double-strand break processing at the repetitive ribosomal DNA array to ensure proper chromosome segregation during meiosis in budding yeast.Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation.BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolismDelineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvaseKdm5/Lid Regulates Chromosome Architecture in Meiotic Prophase I Independently of Its Histone Demethylase ActivityCDK-dependent nuclear localization of B-cyclin Clb1 promotes FEAR activation during meiosis I in budding yeast.Cdc7-Dbf4 is a gene-specific regulator of meiotic transcription in yeastMale hypogonadism and germ cell loss caused by a mutation in Polo-like kinase 4.Polo-like kinase-dependent phosphorylation of the synaptonemal complex protein SYP-4 regulates double-strand break formation through a negative feedback loop.GEN1/Yen1 and the SLX4 complex: Solutions to the problem of Holliday junction resolution.Meiotic recombination intermediates are resolved with minimal crossover formation during return-to-growth, an analogue of the mitotic cell cycleThe meiotic checkpoint network: step-by-step through meiotic prophaseSynaptonemal complex components persist at centromeres and are required for homologous centromere pairing in mouse spermatocytes.Top3-Rmi1 DNA single-strand decatenase is integral to the formation and resolution of meiotic recombination intermediates.A method for sporulating budding yeast cells that allows for unbiased identification of kinase substrates using stable isotope labeling by amino acids in cell culture.DNA double-strand break repair in Caenorhabditis elegansSmc5/6-Mms21 prevents and eliminates inappropriate recombination intermediates in meiosis.Dot1-dependent histone H3K79 methylation promotes the formation of meiotic double-strand breaks in the absence of histone H3K4 methylation in budding yeast.Sporulation in the budding yeast Saccharomyces cerevisiae.Separable Crossover-Promoting and Crossover-Constraining Aspects of Zip1 Activity during Budding Yeast MeiosisCentromere pairing--tethering partner chromosomes in meiosis I.Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast MeiosisIdentification of Putative Mek1 Substrates during Meiosis in Saccharomyces cerevisiae Using Quantitative Phosphoproteomics.Mus81-Mms4 functions as a single heterodimer to cleave nicked intermediates in recombinational DNA repair.Meiotic recombination modulates the structure and dynamics of the synaptonemal complex during C. elegans meiosis.The Genomes of Three Uneven Siblings: Footprints of the Lifestyles of Three Trichoderma Species.akirin is required for diakinesis bivalent structure and synaptonemal complex disassembly at meiotic prophase IThe MAP kinase pathway coordinates crossover designation with disassembly of synaptonemal complex proteins during meiosis.The multiple roles of cohesin in meiotic chromosome morphogenesis and pairing.
P2860
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P2860
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@ast
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@en
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@nl
type
label
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@ast
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@en
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@nl
prefLabel
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@ast
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@en
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@nl
P2860
P3181
P356
P1433
P1476
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis.
@en
P2093
Anuradha Sourirajan
Michael Lichten
P2860
P304
P3181
P356
10.1101/GAD.1711408
P407
P577
2008-10-01T00:00:00Z