Cdc14 targets the Holliday junction resolvase Yen1 to the nucleus in early anaphase

References

• Pâques F, Haber JE. Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. Microbiol Mol Biol Rev 1999; 63:349 - 404; PMID: 10357855
   PubMed Web of Science ®Google Scholar
• Heyer W-D, Ehmsen KT, Liu J. Regulation of homologous recombination in eukaryotes. Annu Rev Genet 2010; 44:113 - 39; http://dx.doi.org/10.1146/annurev-genet-051710-150955; PMID: 20690856
   PubMed Web of Science ®Google Scholar
• Rass U. Resolving branched DNA intermediates with structure-specific nucleases during replication in eukaryotes. Chromosoma 2013; 122:499 - 515; http://dx.doi.org/10.1007/s00412-013-0431-z; PMID: 24008669
   PubMed Web of Science ®Google Scholar
• Schwacha A, Kleckner N. Identification of double Holliday junctions as intermediates in meiotic recombination. Cell 1995; 83:783 - 91; http://dx.doi.org/10.1016/0092-8674(95)90191-4; PMID: 8521495
   PubMed Web of Science ®Google Scholar
• Bzymek M, Thayer NH, Oh SD, Kleckner N, Hunter N. Double Holliday junctions are intermediates of DNA break repair. Nature 2010; 464:937 - 41; http://dx.doi.org/10.1038/nature08868; PMID: 20348905
   PubMed Web of Science ®Google Scholar
• Schwartz EK, Heyer W-D. Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes. Chromosoma 2011; 120:109 - 27; http://dx.doi.org/10.1007/s00412-010-0304-7; PMID: 21369956
   PubMed Web of Science ®Google Scholar
• Hickson ID, Mankouri HW. Processing of homologous recombination repair intermediates by the Sgs1-Top3-Rmi1 and Mus81-Mms4 complexes. Cell Cycle 2011; 10:3078 - 85; http://dx.doi.org/10.4161/cc.10.18.16919; PMID: 21876385
   PubMed Web of Science ®Google Scholar
• Wu L, Hickson ID. The Bloom’s syndrome helicase suppresses crossing over during homologous recombination. Nature 2003; 426:870 - 4; http://dx.doi.org/10.1038/nature02253; PMID: 14685245
   PubMed Web of Science ®Google Scholar
• Kaliraman V, Mullen JR, Fricke WM, Bastin-Shanower SA, Brill SJ. Functional overlap between Sgs1-Top3 and the Mms4-Mus81 endonuclease. Genes Dev 2001; 15:2730 - 40; http://dx.doi.org/10.1101/gad.932201; PMID: 11641278
   PubMed Web of Science ®Google Scholar
• Fricke WM, Brill SJ. Slx1-Slx4 is a second structure-specific endonuclease functionally redundant with Sgs1-Top3. Genes Dev 2003; 17:1768 - 78; http://dx.doi.org/10.1101/gad.1105203; PMID: 12832395
   PubMed Web of Science ®Google Scholar
• Fricke WM, Bastin-Shanower SA, Brill SJ. Substrate specificity of the Saccharomyces cerevisiae Mus81-Mms4 endonuclease. DNA Repair (Amst) 2005; 4:243 - 51; http://dx.doi.org/10.1016/j.dnarep.2004.10.001; PMID: 15590332
   PubMed Web of Science ®Google Scholar
• Ip SCY, Rass U, Blanco MG, Flynn HR, Skehel JM, West SC. Identification of Holliday junction resolvases from humans and yeast. Nature 2008; 456:357 - 61; http://dx.doi.org/10.1038/nature07470; PMID: 19020614
   PubMed Web of Science ®Google Scholar
• Matos J, Blanco MG, Maslen S, Skehel JM, West SC. Regulatory control of the resolution of DNA recombination intermediates during meiosis and mitosis. Cell 2011; 147:158 - 72; http://dx.doi.org/10.1016/j.cell.2011.08.032; PMID: 21962513
   PubMed Web of Science ®Google Scholar
• Schwartz EK, Wright WD, Ehmsen KT, Evans JE, Stahlberg H, Heyer W-D. Mus81-Mms4 functions as a single heterodimer to cleave nicked intermediates in recombinational DNA repair. Mol Cell Biol 2012; 32:3065 - 80; http://dx.doi.org/10.1128/MCB.00547-12; PMID: 22645308
   PubMed Web of Science ®Google Scholar
• Ira G, Malkova A, Liberi G, Foiani M, Haber JE. Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast. Cell 2003; 115:401 - 11; http://dx.doi.org/10.1016/S0092-8674(03)00886-9; PMID: 14622595
   PubMed Web of Science ®Google Scholar
• Oh SD, Lao JP, Hwang PY-H, Taylor AF, Smith GR, Hunter N. BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules. Cell 2007; 130:259 - 72; http://dx.doi.org/10.1016/j.cell.2007.05.035; PMID: 17662941
   PubMed Web of Science ®Google Scholar
• Cromie GA, Hyppa RW, Taylor AF, Zakharyevich K, Hunter N, Smith GR. Single Holliday junctions are intermediates of meiotic recombination. Cell 2006; 127:1167 - 78; http://dx.doi.org/10.1016/j.cell.2006.09.050; PMID: 17174892
   PubMed Web of Science ®Google Scholar
• Kaliraman V, Brill SJ. Role of SGS1 and SLX4 in maintaining rDNA structure in Saccharomyces cerevisiae. Curr Genet 2002; 41:389 - 400; http://dx.doi.org/10.1007/s00294-002-0319-6; PMID: 12228808
   PubMed Web of Science ®Google Scholar
• Gaillard P-HL, Noguchi E, Shanahan P, Russell P. The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism. Mol Cell 2003; 12:747 - 59; http://dx.doi.org/10.1016/S1097-2765(03)00342-3; PMID: 14527419
   PubMed Web of Science ®Google Scholar
• Tay YD, Wu L. Overlapping roles for Yen1 and Mus81 in cellular Holliday junction processing. J Biol Chem 2010; 285:11427 - 32; http://dx.doi.org/10.1074/jbc.M110.108399; PMID: 20178992
   PubMed Web of Science ®Google Scholar
• Ho CK, Mazón G, Lam AF, Symington LS. Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast. Mol Cell 2010; 40:988 - 1000; http://dx.doi.org/10.1016/j.molcel.2010.11.016; PMID: 21172663
   PubMed Web of Science ®Google Scholar
• Ashton TM, Mankouri HW, Heidenblut A, McHugh PJ, Hickson ID. Pathways for Holliday junction processing during homologous recombination in Saccharomyces cerevisiae. Mol Cell Biol 2011; 31:1921 - 33; http://dx.doi.org/10.1128/MCB.01130-10; PMID: 21343337
   PubMed Web of Science ®Google Scholar
• Mazón G, Lam AF, Ho CK, Kupiec M, Symington LS. The Rad1-Rad10 nuclease promotes chromosome translocations between dispersed repeats. Nat Struct Mol Biol 2012; 19:964 - 71; http://dx.doi.org/10.1038/nsmb.2359; PMID: 22885325
   PubMed Web of Science ®Google Scholar
• Szakal B, Branzei D. Premature Cdk1/Cdc5/Mus81 pathway activation induces aberrant replication and deleterious crossover. EMBO J 2013; 32:1155 - 67; http://dx.doi.org/10.1038/emboj.2013.67; PMID: 23531881
   PubMed Web of Science ®Google Scholar
• Gallo-Fernández M, Saugar I, Ortiz-Bazán MÁ, Vázquez MV, Tercero JA. Cell cycle-dependent regulation of the nuclease activity of Mus81-Eme1/Mms4. Nucleic Acids Res 2012; 40:8325 - 35; http://dx.doi.org/10.1093/nar/gks599; PMID: 22730299
   PubMed Web of Science ®Google Scholar
• Matos J, Blanco MG, West SC. Cell-Cycle Kinases Coordinate the Resolution of Recombination Intermediates with Chromosome Segregation. Cell Rep 2013;1–11.
   Google Scholar
• Kosugi S, Hasebe M, Tomita M, Yanagawa H. Systematic identification of cell cycle-dependent yeast nucleocytoplasmic shuttling proteins by prediction of composite motifs. Proc Natl Acad Sci U S A 2009; 106:10171 - 6; http://dx.doi.org/10.1073/pnas.0900604106; PMID: 19520826
   PubMed Web of Science ®Google Scholar
• Loog M, Morgan DO. Cyclin specificity in the phosphorylation of cyclin-dependent kinase substrates. Nature 2005; 434:104 - 8; http://dx.doi.org/10.1038/nature03329; PMID: 15744308
   PubMed Web of Science ®Google Scholar
• Visintin R, Craig K, Hwang ES, Prinz S, Tyers M, Amon A. The phosphatase Cdc14 triggers mitotic exit by reversal of Cdk-dependent phosphorylation. Mol Cell 1998; 2:709 - 18; http://dx.doi.org/10.1016/S1097-2765(00)80286-5; PMID: 9885559
   PubMed Web of Science ®Google Scholar
• Jin F, Liu H, Liang F, Rizkallah R, Hurt MM, Wang Y. Temporal control of the dephosphorylation of Cdk substrates by mitotic exit pathways in budding yeast. Proc Natl Acad Sci U S A 2008; 105:16177 - 82; http://dx.doi.org/10.1073/pnas.0808719105; PMID: 18845678
   PubMed Web of Science ®Google Scholar
• Stegmeier F, Amon A. Closing mitosis: the functions of the Cdc14 phosphatase and its regulation. Annu Rev Genet 2004; 38:203 - 32; http://dx.doi.org/10.1146/annurev.genet.38.072902.093051; PMID: 15568976
   PubMed Web of Science ®Google Scholar
• Rock JM, Amon A. The FEAR network. Curr Biol 2009; 19:R1063 - 8; http://dx.doi.org/10.1016/j.cub.2009.10.002; PMID: 20064401
   PubMed Web of Science ®Google Scholar
• Ross KE, Cohen-Fix O. A role for the FEAR pathway in nuclear positioning during anaphase. Dev Cell 2004; 6:729 - 35; http://dx.doi.org/10.1016/S1534-5807(04)00128-5; PMID: 15130497
   PubMed Web of Science ®Google Scholar
• Sullivan M, Higuchi T, Katis VL, Uhlmann F. Cdc14 phosphatase induces rDNA condensation and resolves cohesin-independent cohesion during budding yeast anaphase. Cell 2004; 117:471 - 82; http://dx.doi.org/10.1016/S0092-8674(04)00415-5; PMID: 15137940
   PubMed Web of Science ®Google Scholar
• Torres-Rosell J, Machín F, Jarmuz A, Aragón L. Nucleolar segregation lags behind the rest of the genome and requires Cdc14p activation by the FEAR network. Cell Cycle 2004; 3:496 - 502; http://dx.doi.org/10.4161/cc.3.4.802; PMID: 15004526
   PubMed Web of Science ®Google Scholar
• Machín F, Torres-Rosell J, Jarmuz A, Aragón L. Spindle-independent condensation-mediated segregation of yeast ribosomal DNA in late anaphase. J Cell Biol 2005; 168:209 - 19; http://dx.doi.org/10.1083/jcb.200408087; PMID: 15657393
   PubMed Web of Science ®Google Scholar
• Khmelinskii A, Lawrence C, Roostalu J, Schiebel E. Cdc14-regulated midzone assembly controls anaphase B. J Cell Biol 2007; 177:981 - 93; http://dx.doi.org/10.1083/jcb.200702145; PMID: 17562791
   PubMed Web of Science ®Google Scholar
• Jaspersen SL, Charles JF, Tinker-Kulberg RL, Morgan DO. A late mitotic regulatory network controlling cyclin destruction in Saccharomyces cerevisiae. Mol Biol Cell 1998; 9:2803 - 17; http://dx.doi.org/10.1091/mbc.9.10.2803; PMID: 9763445
   PubMed Web of Science ®Google Scholar
• Jaspersen SL, Morgan DO. Cdc14 activates cdc15 to promote mitotic exit in budding yeast. Curr Biol 2000; 10:615 - 8; http://dx.doi.org/10.1016/S0960-9822(00)00491-7; PMID: 10837230
   PubMed Web of Science ®Google Scholar
• Sanchez-Diaz A, Nkosi PJ, Murray S, Labib K. The Mitotic Exit Network and Cdc14 phosphatase initiate cytokinesis by counteracting CDK phosphorylations and blocking polarised growth. EMBO J 2012; 31:3620 - 34; http://dx.doi.org/10.1038/emboj.2012.224; PMID: 22872148
   PubMed Web of Science ®Google Scholar
• Shou W, Seol JH, Shevchenko A, Baskerville C, Moazed D, Chen ZW, Jang J, Shevchenko A, Charbonneau H, Deshaies RJ. Exit from mitosis is triggered by Tem1-dependent release of the protein phosphatase Cdc14 from nucleolar RENT complex. Cell 1999; 97:233 - 44; http://dx.doi.org/10.1016/S0092-8674(00)80733-3; PMID: 10219244
   PubMed Web of Science ®Google Scholar
• Ghaemmaghami S, Huh W-K, Bower K, Howson RW, Belle A, Dephoure N, O’Shea EK, Weissman JS. Global analysis of protein expression in yeast. Nature 2003; 425:737 - 41; http://dx.doi.org/10.1038/nature02046; PMID: 14562106
   PubMed Web of Science ®Google Scholar
• D’Amours D, Stegmeier F, Amon A. Cdc14 and condensin control the dissolution of cohesin-independent chromosome linkages at repeated DNA. Cell 2004; 117:455 - 69; http://dx.doi.org/10.1016/S0092-8674(04)00413-1; PMID: 15137939
   PubMed Web of Science ®Google Scholar
• Hennessy KM, Lee A, Chen E, Botstein D. A group of interacting yeast DNA replication genes. Genes Dev 1991; 5:958 - 69; http://dx.doi.org/10.1101/gad.5.6.958; PMID: 2044962
   PubMed Web of Science ®Google Scholar
• Dulev S, de Renty C, Mehta R, Minkov I, Schwob E, Strunnikov A. Essential global role of CDC14 in DNA synthesis revealed by chromosome underreplication unrecognized by checkpoints in cdc14 mutants. Proc Natl Acad Sci U S A 2009; 106:14466 - 71; http://dx.doi.org/10.1073/pnas.0900190106; PMID: 19666479
   PubMed Web of Science ®Google Scholar
• Janke C, Magiera MM, Rathfelder N, Taxis C, Reber S, Maekawa H, Moreno-Borchart A, Doenges G, Schwob E, Schiebel E, et al. A versatile toolbox for PCR-based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes. Yeast 2004; 21:947 - 62; http://dx.doi.org/10.1002/yea.1142; PMID: 15334558
   PubMed Web of Science ®Google Scholar
• Quevedo O, García-Luis J, Matos-Perdomo E, Aragón L, Machín F. Nondisjunction of a single chromosome leads to breakage and activation of DNA damage checkpoint in G2. PLoS Genet 2012; 8:e1002509; http://dx.doi.org/10.1371/journal.pgen.1002509; PMID: 22363215
   PubMed Web of Science ®Google Scholar