MCB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Park, J.-E.
Right arrow Articles by Lee, K. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Park, J.-E.
Right arrow Articles by Lee, K. S.
Molecular and Cellular Biology, November 2004, p. 9873-9886, Vol. 24, No. 22
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.22.9873-9886.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Novel Functional Dissection of the Localization-Specific Roles of Budding Yeast Polo Kinase Cdc5p

Jung-Eun Park,1,2 Chong J. Park,1 Krisada Sakchaisri,1,3 Tatiana Karpova,4 Satoshi Asano,1 James McNally,4 Yangil Sunwoo,2 Sun-Hee Leem,2 and Kyung S. Lee1*

Laboratory of Metabolism,1 Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland,4 Department of Biology, Dong-A University, Busan, Korea,2 Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok, Thailand3

Received 18 May 2004/ Accepted 30 July 2004

Budding yeast polo kinase Cdc5p localizes to the spindle pole body (SPB) and to the bud-neck and plays multiple roles during M-phase progression. To dissect localization-specific mitotic functions of Cdc5p, we tethered a localization-defective N-terminal kinase domain of Cdc5p (Cdc5p{Delta}C) to the SPB or to the bud-neck with components specifically localizing to one of these sites and characterized these mutants in a cdc5{Delta} background. Characterization of a viable, SPB-localizing, CDC5{Delta}C-CNM67 mutant revealed that it is defective in timely degradation of Swe1p, a negative regulator of Cdc28p. Loss of BFA1, a negative regulator of mitotic exit, rescued the lethality of a neck-localizing CDC5{Delta}C-CDC12 or CDC5{Delta}C-CDC3 mutant but yielded severe defects in cytokinesis. These data suggest that the SPB-associated Cdc5p activity is critical for both mitotic exit and cytokinesis, whereas the bud neck-localized Cdc5p is required for proper Swe1p regulation. Interestingly, a cdc5{Delta} bfa1{Delta} swe1{Delta} triple mutant is viable but grows slowly, whereas cdc5{Delta} cells bearing both CDC5{Delta}C-CNM67 and CDC5{Delta}C-CDC12 grow well with only a mild cell cycle delay. Thus, SPB- and the bud-neck-localized Cdc5p control most of the critical Cdc5p functions and downregulation of Bfa1p and Swe1p at the respective locations are two critical factors that require Cdc5p.


* Corresponding author. Mailing address: Laboratory of Metabolism, National Cancer Institute, NIH, 9000 Rockville Pike, Bldg. 37, Rm. 3118, Bethesda, MD 20892. Phone: (301) 496-9635. Fax: (301) 496-8419. E-mail: kyunglee{at}pop.nci.nih.gov.


Molecular and Cellular Biology, November 2004, p. 9873-9886, Vol. 24, No. 22
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.22.9873-9886.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2004 by the American Society for Microbiology. All rights reserved.