Erratum: Fcp1-dependent dephosphorylation is required for M-phase-promoting factor inactivation at mitosis exit (Nature Communications (2012) 7 (894) DOI: 10.1038/ncomms1886);Fcp1-dependent dephosphorylation is required for M-phase-promoting factor inactivation at mitosis exit

Nature Communications

Volumn 3, Issue , 2012, Pages

  Visconti, Roberta ^a,b   Palazzo, Luca ^a,c   Della Monica, Rosa ^a,c   Grieco, Domenico ^a,c  

^a CEINGE BIOTECNOLOGIE AVANZATE   (Italy)

^b CNR   (Italy)

^c UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CELL CYCLE PROTEIN 20; CELL PROTEIN; CYCLINE; MATURATION PROMOTING FACTOR; PHOSPHOTRANSFERASE; PROTEIN FCP1; RNA POLYMERASE II; UNCLASSIFIED DRUG; WEE1 ENZYME; CARBOXY TERMINAL DOMAIN PHOSPHATASE; CARBOXY-TERMINAL DOMAIN PHOSPHATASE; CDC20 PROTEIN, HUMAN; CELL CYCLE PROTEIN; NUCLEAR PROTEIN; PHOSPHOPROTEIN PHOSPHATASE; PROTEIN TYROSINE KINASE; PROTEINASE; UBIQUITIN SPECIFIC PROTEASE; UBIQUITIN-SPECIFIC PROTEASE; WEE1 PROTEIN, HUMAN;

ANAPHASE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL CYCLE M PHASE; DEPHOSPHORYLATION; HUMAN; HUMAN CELL; MITOSIS; GENETICS; HELA CELL; METABOLISM; PHOSPHORYLATION; PHYSIOLOGY;

EUKARYOTA;

CELL CYCLE PROTEINS; ENDOPEPTIDASES; HELA CELLS; HUMANS; MATURATION-PROMOTING FACTOR; MITOSIS; NUCLEAR PROTEINS; PHOSPHOPROTEIN PHOSPHATASES; PHOSPHORYLATION; PROTEIN-TYROSINE KINASES;

EID: 84863309216     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms2363     Document Type: Erratum

References (31)

1. Bollen, M., Gerligh, D. W. & Lasage, B. Mitotic phosphatases: from entry guards to exit guides. Trends Cell Biol. 19 531-541 (2009).
2. Kapuy, O., He, E., Uhlmann, F. & Novák, B. Mitotic exit in mammalian cells. Mol. Syst. Biol. 5 324 (2009).
3. Novak, B. & Tyson, J. J. Numerical analysis of a comprehensive model of M-phase control in Xenopus oocyte extracts and intact embryos. J. Cell Sci. 106 1153-1168 (1993). (Pubitemid 24018401)
4. Musacchio, A. & Salmon, E. D. The spindle-assembly checkpoint in space and time. Nat. Rev. Mol. Cell. Biol. 8 379-393 (2007). (Pubitemid 46643240)
5. Okamoto, K. & Sagata, N. Mechanism for inactivation of the mitotic inhibitory kinase Wee1 at M phase. Proc. Natl Acad. Sci. USA 104 3753-3758 (2007). (Pubitemid 47181527)
6. Nakajima, H., Toyoshima-Morimoto, F., Taniguchi, E. & Nishida, E. Identification of a consensus motif for Plk (Polo-like kinase) phosphorylation reveals Myt1 as a Plk1 substrate. J. Biol. Chem. 278 25277-25280 (2003). (Pubitemid 36835273)
7. Izumi, T. & Maller, J. L. Elimination of cdc2 phosphorylation sites in the cdc25 phosphatase blocks initiation of M-phase. Mol. Biol. Cell 4 1337-1350 (1993). (Pubitemid 24045763)
8. Li, C., Andrake, M., Dunbrack, R. & Enders, G. H. A bifunctional regulatory element in human somatic Wee1 mediates cyclin A/Cdk2 binding and Crm1-dependent nuclear export. Mol. Cell. Biol. 30 116-130 (2010).
9. D'Angiolella, V., Palazzo, L., Santarpia, C., Costanzo, V. & Grieco, D. Role for non-proteolytic control of M-phase-promoting factor activity at M-phase exit. PLoS One 2 e247 (2007).
10. Stegmeier, F. et al. Anaphase initiation is regulated by antagonistic ubiquitination and deubiquitination activities. Nature 446 876-881 (2007).
11. D'Angiolella, V., Mari, C., Nocera, D., Rametti, L. & Grieco, D. The spindle checkpoint requires cyclin-dependent kinase activity. Genes Dev. 17 2520-2525 (2003). (Pubitemid 37271422)
12. Tang, Z., Shu, H., Oncel, D., Chen, S. & Yu, H. Phosphorylation of Cdc20 by Bub1 provides a catalytic mechanism for APC/C inhibition by the spindle checkpoint. Mol. Cell. 16 387-397 (2004). (Pubitemid 39504793)
13. Skoufias, D. A., Indorato, R. L., Lacroix, F., Panopoulos, A. & Margolis, R. L. Mitosis persists in the absence of Cdk1 activity when proteolysis or protein phosphatase activity is suppressed. J. Cell Biol. 179 671-685 (2007). (Pubitemid 350146254)
14. Wu, J. Q. et al. PP1-mediated dephosphorylation of phosphoproteins at mitotic exit is controlled by inhibitor-1 and PP1 phosphorylation. Nat. Cell Biol. 11 644-651 (2009).
15. Son, S. & Osmani, S. A. Analysis of all protein phosphatase genes in Aspergillus nidulans identifies a new mitotic regulator, fcp1. Eukaryot. Cell 8 573-585 (2009).
16. Archambault, J. et al. FCP1, the RAP74-interacting subunit of a human protein phosphatase that dephosphorylates the carboxyl-terminal domain of RNA polymerase IIO. J. Biol. Chem. 273 27593-27601 (1998). (Pubitemid 28500482)
17. Amente, S. et al. Identification of proteins interacting with the RNAPII FCP1 phosphatase: FCP1 forms a complex with arginine methyltransferase PRMT5 and it is a substrate for PRMT5-mediated methylation. FEBS Lett. 579 683-689 (2005).
18. Braunstein, I., Miniowitz, S., Moshe, Y. & Hershko, A. Inhibitory factors associated with anaphase promoting complex/cylosome in mitotic checkpoint. Proc. Natl Acad. Sci. USA 104 4870-4875 (2007). (Pubitemid 47186143)
19. Reddy, S. K., Rape, M., Margansky, W. A. & Kirschner, M. W. Ubiquitination by the anaphase-promoting complex drives spindle checkpoint inactivation. Nature 446 921-925 (2007). (Pubitemid 46633168)
20. Santaguida, S., Tighe, A., D'Alise, A. M., Taylor, S. S. & Musacchio, A. Dissecting the role of MPS1 in chromosome biorientation and the spindle checkpoint through the small molecule inhibitor reversine. J. Cell Biol. 190 73-87 (2010).
21. Visconti, R., Palazzo, L. & Grieco, D. Requirement for proteolysis in spindle assembly checkpoint silencing. Cell Cycle 9 564-569 (2010).
22. Zeng, X. et al. Pharmacologic inhibition of the Anaphase-Promoting Complex induces a spindle checkpoint-dependent mitotic arrest in the absence of spindle damage. Cancer Cell 18 382-395 (2010).
23. Chan, F. L. et al. Active transcription and essential role of RNA polymerase II at the centromere during mitosis. Proc. Natl Acad. Sci. USA 109 1979-1984 (2012).
24. Acquaviva, C., Herzog, F., Kraft, C. & Pines, J. The anaphase promoting complex/cyclosome is recruited to centromeres by the spindle assembly checkpoint. Nat. Cell Biol. 6 892-898 (2004). (Pubitemid 39207254)
25. Howell, B. J. et al. Cytoplasmic dynein/dynactin drives kinetochore protein transport to the spindle poles and has a role in mitotic spindle checkpoint inactivation. J. Cell Biol. 155 1159-1172 (2001). (Pubitemid 34286267)
26. Mochida, S., Maslen, S. L., Skehel, M. & Hunt, T. Greatwall phosphorylates an inhibitor of protein phosphatase 2A that is essential for mitosis. Science 330 1670-1673 (2010).
27. Gharbi-Ayachi, A. et al. The substrate of greatwall kinase, Arpp19, controls mitosis by inhibiting protein phosphatase 2A. Science 330 1673-1676 (2010).
28. Clute, P. & Pines, J. Temporal and spatial control of cyclin B1 destruction in metaphase. Nat. Cell Biol. 1 82-87 (1999). (Pubitemid 129501948)
29. Gebara, M. M., Sayre, M. H. & Corden, J. L. Phosphorylation of the carboxy-terminal repeat domain in RNA polymerase II by cyclin-dependent kinases is sufficient to inhibit transcription. J. Cell. Biochem. 64 390-402 (1997). (Pubitemid 27098625)
30. Palancade, B., Dubois, M. F., Dahmus, M. E. & Bensaude, O. Transcription-independent RNA polymerase II dephosphorylation by the FCP1 carboxy-terminal domain phosphatase in Xenopus laevis early embryos. Mol. Cell. Biol. 21 6359-6368 (2001). (Pubitemid 32927405)
31. Cohen, P., Klumpp, S. & Schelling, D. L. An improved procedure for identifying and quantitating protein phosphatases in mammalian tissues. FEBS Lett. 250 596-600 (1989). (Pubitemid 19171416)