[1] Mocciaro A, Schiebel E. Cdc14 highly conserved family of phosphatases with non-conserved function[J]. J Cell Sci, 2010, 123(Pt 17):2867-2876. [2] Kuilman T, Maiolica A, Godfrey M, et al. Identification of Cdk targets that control cytokinesis[J]. EMBO J, 2015,34(1):81-96. [3] Godfrey M, Kuilman T, Uhlmann F. Nur1 dephosphorylation confers positive feedback to mitotic exit phosphatase activation in budding yeast[J]. PLoS Genet, 2015, 11(1):e1004907. [4] Listovsky T, Zor A, Laronne A, et al. Cdk1 is essential for mammalian cyclosome/APC regulation[J]. Exp Cell Res, 2000, 255(2):184-191. [5] Mailand N, Lukas C, Kaiser BK, et al. Deregulated human Cdc14A phosphatase disrupts centrosome separation and chromosome segregation[J]. Nat Cell Biol, 2002, 4(4):317-322. [6] Gruneberg U, Glotzer M, Gartner A, et al. The CeCDC-14 phosphatase is required for cytokinesis in the Caenorhabditis elegans embryo[J]. J Cell Biol, 2002,158(5):901-914. [7] Bizzari F, Marston AL:Cdc55 coordinates spindle assembly and chromosome disjunction during meiosis[J]. J Cell Biol, 2011, 193(7):1213-1228. [8] Avena JS, Burns S, Yu Z, et al. Licensing of yeast centrosome duplication requires phosphoregulation of sfi1[J]. PLoS Genet, 2014, 10(10):e1004666. [9] Argüello-Miranda O, Zagoriy I, Mengoli V, et al. Casein kinase 1 coordinates cohesin cleavage, gametogenesis, and exit from M phase in meiosisⅡ[J]. Dev Cell, 2017, 40(1):37-52. [10] Maekawa H, Priest C, Lechner J, et al. The yeast centrosome translates the positional information of the anaphase spindle into a cell cycle signal[J]. J Cell Biol, 2007, 179(3):423-436. [11] Marston A. Cdc14 phosphatase directs centrosome re-duplication at the meiosisⅠ to meiosisⅡ transition in budding yeast[M]. Wellcome Open Res, 2017,2:2. [12] Esteban V, Blanco M, Cueille N, et al. A role for the Cdc14-family phosphatase Flp1p at the end of the cell cycle in controlling the rapid degradation of the mitotic inducer Cdc25p in fission yeast[J]. J Cell Sci, 2004, 117(Pt 12):2461-2468. [13] Cueille N, Salimova E, Esteban V, et al. Flp1, a fission yeast orthologue of the S. cerevisiae CDC14 gene, is not required for cyclin degradation or rum1p stabilisation at the end of mitosis[J]. J Cell Sci, 2001, 114(Pt14):2649-2664. [14] Benjamin AW, Kathleen LG. Fission yeast Clp1p phosphatase affects G2/M transition and mitotic exit through Cdc25p inactivation[J]. EMBO J, 2004, 23(4):919-929. [15] Schindler K, Schultz RM. The CDC14A phosphatase regulates oocyte maturation in mouse[J]. Cell Cycle, 2009, 8(7):1090-1098. [16] Manzoni R,Montani F, Visintin C, et al. Oscillations in Cdc14 release and Sequestration reveal a circuit underlying mitotic exit[J]. J Cell Biol, 2010, 190(2):209-222. [17] Bloom J, Cristea IM, Procko AL, et al. Global analysis of Cdc14 phosphatase reveals diverse roles in mitotic processes[J]. J Biol Chem, 2011, 286(7):5434-5445. [18] Kao L, Wang YT, Chen YC, et al. Global analysis of cdc14 dephosphorylation sites reveals essential regulatory role in mitosis and cytokinesis[J]. Mol Cell Proteomics, 2014, 13(2):594-605. [19] Miller DP, Hall H, Chaparian R, et al. Dephosphorylation of Iqg1 by Cdc14 regulates cytokinesis in budding yeast[J]. Mol Biol Cell, 2015, 26(16):2913-2926. [20] Ann Marie EF, Catherine CLW, John RY, et al. The FEAR protein Slk19 restricts Cdc14 phosphatase to the nucleus until the end of anaphase, regulating its participation in mitotic exit in saccharomyces cerevisiae[J]. PLoS One, 2013, 8(9):e73194. [21] Mohl DA, Huddleston MJ, Collingwood TS, et al. Dbf2-Mob1 drives relocalization of protein phosphatase Cdc14 to the cytoplasm during exit from mitosis[J]. J Cell Biol, 2009, 184(4):527-539. [22] Kaiser BK, Zimmerman ZA, Charbonneau H, et al. Disruption of centrosome structure,chromosome segregation,and cytokinesis by misexpression of human Cdc14A phosphatase[J]. Mol Biol Cell, 2002, 13(7):2289-2300. [23] Vázquez-Novelle MD, Mailand N, Ovejero S,et al. Human Cdc14A phosphatase modulates the G2/M transition through Cdc25A and Cdc25B[J]. J Biol Chem, 2010, 285(52):40544-40553. [24] Sacristán MP,Overjero S,Bueno A. Human Cdc14A becomes a cell cycle gene in controlling Cdk1 activity at the G2/M transition[J]. Cell Cycle, 2011, 10(3):387-391. [25] Villoria MT, Ramos F, Dueñas E, et al. Stabilization of the metaphase spindle by Cdc14 is required for recombinational DNA repair[J].EMBO J, 2017, 36(1):79-101. [26] Blanco MG, Matos J, West SC. Dual control of Yen1 nuclease activity and cellular localization by Cdk and Cdc14 prevents genome instability[J]. Mol Cell, 2014, 54(1):94-106. [27] Eissler CL, Mazón G, Powers BL, et al. The Cdk/cDc14 module controls activation of the Yen1 Holliday junction resolvase to promote genome stability[J]. Mol Cell, 2014, 54(1):80-93. [28] García-Luis J, Clemente-Blanco A, Aragón L, et al. Cdc14 targets the Holliday junction resolvase Yen1 to the nucleus in early anaphase[J]. Cell Cycle, 2014, 13(9):1392-1399. [29] Paulsen MT, Starks AM, Derheimer FA, et al. The p53-targeting human phosphatase hCDC14A interacts with the CDK1/cyclin B complex and is differentially expressed in human cancers[J]. Mol Cancer, 2006, 5:25. [30] Asada M, Ohmi K, Delia D, et al. BRAP2 functions as a cytoplasm ic retention protein for p21 during monocyte differentiation[J]. Mol Cell Biol, 2004, 24(18):8236-8243. [31] Li S, Ku CY, Farmer AA, et al. Identification of a novel cytoplasmic protein MP[J]. J Biol Chem, 1998, 273(11):6183-6189. [32] Matheny SA, Chen C, Kortum RL, et al. Ras regulates assembly of mitogenic signalling complexes through the effector protein IMP[J]. Nature, 2004, 427(6971):256-260. [33] Diep CH, Daniel AR, Mauro LJ, et al. Progesterone action in breast, uterine, and ovarian cancers[J]. J Mol Endocrinol, 2015, 54(2):R31-R53. [34] Tsuruta T, Kozaki K, Uesugi A, et al. miR-152 is a tumor suppressor microRNA that is silenced by DNA hypermethylation in endometrial cancer[J]. Cancer Res, 2011, 71(20):6450-6462. [35] Kao L, Wang YT, Chen YC, et al. Global analysis of cdc14 dephosphorylation Sites reveals essential regulatory role in mitosis and cytokinesis[J]. Mol Cell Proteomics, 2014, 13(2):594-605. |