Eukaryotic Cell
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Eukaryotic Cell, October 2007, p. 1814-1823, Vol. 6, No. 10
1535-9778/07/$08.00+0     doi:10.1128/EC.00087-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Regulation of Phosphoinositide Levels by the Phospholipid Transfer Protein Sec14p Controls Cdc42p/p21-Activated Kinase-Mediated Cell Cycle Progression at Cytokinesis{triangledown}

Alicia G. Howe,1 Gregory D. Fairn,1 Kendra MacDonald,1 Vytas A. Bankaitis,2 and Christopher R. McMaster1*

Atlantic Research Centre, Departments of Pediatrics and Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia B3H 4H7, Canada,1 Department of Cell and Developmental Biology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 275992

Received 19 March 2007/ Accepted 18 June 2007

Sec14p is an essential phosphatidylcholine/phosphatidylinositol transfer protein with a well-described role in the regulation of Golgi apparatus-derived vesicular transport in yeast. Inactivation of the CDP-choline pathway for phosphatidylcholine synthesis allows cells to survive in the absence of Sec14p function through restoration of Golgi vesicular transport capability. In this study, Saccharomyces cerevisiae cells containing a SEC14 temperature-sensitive allele along with an inactivated CDP-choline pathway were transformed with a high-copy-number yeast genomic library. Genes whose increased expression inhibited cell growth in the absence of Sec14p function were identified. Increasing levels of the Rho GTPase Cdc42p and its direct effector kinases Cla4p and Ste20p prevented the growth of cells lacking Sec14p and CDP-choline pathway function. Growth suppression was accompanied by an increase in large and multiply budded cells. This effect on polarized cell growth did not appear to be due to an inability to establish cell polarity, since both the actin cytoskeleton and localization of the septin Cdc12p were unaffected by increased expression of Cdc42p, Cla4p, or Ste20p. Nuclei were present in both the mother cell and the emerging bud, consistent with Sec14p regulation of the cell cycle subsequent to anaphase but prior to cytokinesis/septum breakdown. Increased expression of phosphatidylinositol 4-kinases and phosphatidylinositol 4-phosphate 5-kinase prevented growth arrest by CDC42, CLA4, or STE20 upon inactivation of Sec14p function. Sec14p regulation of phosphoinositide levels affects cytokinesis at the level of the Cdc42p/Cla4p/Ste20p signaling cascade.


* Corresponding author. Mailing address: Atlantic Research Centre, Dalhousie University, 5849 University Ave., Rm. C302, Halifax, Nova Scotia B3H 4H7, Canada. Phone: (902) 494-2953. Fax: (902) 494-1394. E-mail: christopher.mcmaster{at}dal.ca

{triangledown} Published ahead of print on 29 June 2007.


Eukaryotic Cell, October 2007, p. 1814-1823, Vol. 6, No. 10
1535-9778/07/$08.00+0     doi:10.1128/EC.00087-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.




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