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Novel functional dissection of the localization-specific roles of budding yeast polo kinase Cdc5p

  • Jung Eun Park
  • , Chong J. Park
  • , Krisada Sakchaisri
  • , Tatiana Karpova
  • , Satoshi Asano
  • , James McNally
  • , Yangil Sunwoo
  • , Sun Hee Leem
  • , Kyung S. Lee
  • National Cancer Institute (NCI)
  • Dong-A University
  • Mahidol University

Research output: Contribution to journal › Article › peer-review

32 Citations (Scopus)

Abstract

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 (Cdc5pΔC) to the SPB or to the bud-neck with components specifically localizing to one of these sites and characterized these mutants in a cdc5Δ background. Characterization of a viable, SPB-localizing, CDC5ΔC-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 CDC5ΔC-CDC12 or CDC5ΔC-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 cdc5Δ bfa1Δ swe1Δ triple mutant is viable but grows slowly, whereas cdc5Δ cells bearing both CDC5ΔC-CNM67 and CDC5ΔC-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.

Original languageEnglish
Pages (from-to)9873-9886
Number of pages14
JournalMolecular and Cellular Biology
Volume24
Issue number22
DOIs
Publication statusPublished - Nov 2004
Externally publishedYes

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