Genetics, Vol. 153, 1561-1572, December 1999, Copyright © 1999

The Identification of Wos2, a p23 Homologue That Interacts With Wee1 and Cdc2 in the Mitotic Control of Fission Yeasts

Manuel J. Muñoza, Eduardo R. Bejaranoa, Rafael R. Dagaa, and Juan Jimeneza
a Departamento de Genética, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga, Spain

Corresponding author: Juan Jimenez, Departamento de Genética, Facultad de Ciencias, Universidad de Málaga, Campus Universitario de Teatinos, 29071 Málaga, Spain., jimmar{at}uma.es (E-mail)

Communicating editor: P. G. YOUNG

The Wee1 kinase inhibits entry into mitosis by phosphorylation of the Cdc2 kinase. Searching for multicopy suppressors that abolish this inhibition in the fission yeast, we have identified a novel gene, here named wos2, encoding a protein with significant homology to human p23, an Hsp90-associated cochaperone. The deletion mutant has a modest phenotype, being heat-shock sensitive. Using antibodies raised against bacterially produced protein, we determined that Wos2 is very abundant, ubiquitously distributed in the yeast cell, and its expression dropped drastically as cells entered into early stationary phase, indicating that its function is associated with cell proliferation. In proliferating cells, the amount of Wos2 protein was not subjected to cell cycle regulation. However, in vitro assays demonstrated that this Hsp90 cochaperone is potentially regulated by phosphorylation. In addition to suppressing Wee1 activity, overproduction of Wos2 displayed synthetic lethality with Cdc2 mutant proteins, indicating that this Hsp90 cochaperone functionally interacts with Cdc2. The level of Cdc2 protein and its associated H1 kinase activity under synthetic lethal conditions suggested a regulatory role for this Wos2-Cdc2 interaction. Hsp90 complexes are required for CDK regulation; the synergy found between the excess of Wos2 and a deficiency in Hsp90 activity suggests that Wos2 could specifically interfere with the Hsp90-dependent regulation of Cdc2. In vitro analysis indicated that the above genetic interactions could take place by physical association of Wos2 with the single CDK complex of the fission yeast. Expression of the budding yeast p23 protein (encoded by the SBA1 gene) in the fission yeast indicated that Wos2 and Sba1 are functionally exchangeable and therefore that properties described here for Wos2 could be of wide significance in understanding the biological function of cochaperone p23 in eukaryotic cells.





This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
F. Forafonov, O. A. Toogun, I. Grad, E. Suslova, B. C. Freeman, and D. Picard
p23/Sba1p Protects against Hsp90 Inhibitors Independently of Its Intrinsic Chaperone Activity
Mol. Cell. Biol., May 15, 2008; 28(10): 3446 - 3456.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
S. Huard, R. T. Elder, D. Liang, G. Li, and R. Y. Zhao
Human Immunodeficiency Virus Type 1 Vpr Induces Cell Cycle G2 Arrest through Srk1/MK2-Mediated Phosphorylation of Cdc25
J. Virol., March 15, 2008; 82(6): 2904 - 2917.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
V. T. George, G. Brooks, and T. C. Humphrey
Regulation of Cell Cycle and Stress Responses to Hydrostatic Pressure in Fission Yeast
Mol. Biol. Cell, October 1, 2007; 18(10): 4168 - 4179.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. K. Lovgren, M. Kovarova, and B. H. Koller
cPGES/p23 Is Required for Glucocorticoid Receptor Function and Embryonic Growth but Not Prostaglandin E2 Synthesis
Mol. Cell. Biol., June 15, 2007; 27(12): 4416 - 4430.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
I. Grad, T. A. McKee, S. M. Ludwig, G. W. Hoyle, P. Ruiz, W. Wurst, T. Floss, C. A. Miller III, and D. Picard
The Hsp90 Cochaperone p23 Is Essential for Perinatal Survival
Mol. Cell. Biol., December 1, 2006; 26(23): 8976 - 8983.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
D. M. Price, Z. Jin, S. Rabinovitch, and S. D. Campbell
Ectopic Expression of the Drosophila Cdk1 Inhibitory Kinases, Wee1 and Myt1, Interferes With the Second Mitotic Wave and Disrupts Pattern Formation During Eye Development
Genetics, June 1, 2002; 161(2): 721 - 731.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. Tahbaz, J. B. Carmichael, and T. C. Hobman
GERp95 Belongs to a Family of Signal-transducing Proteins and Requires Hsp90 Activity for Stability and Golgi Localization
J. Biol. Chem., November 9, 2001; 276(46): 43294 - 43299.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. J. Weaver, W. P. Sullivan, S. J. Felts, B. A. L. Owen, and D. O. Toft
Crystal Structure and Activity of Human p23, a Heat Shock Protein 90 Co-chaperone
J. Biol. Chem., July 21, 2000; 275(30): 23045 - 23052.
[Abstract] [Full Text] [PDF]