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A more recent version of this article appeared on July 1, 2006
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Submitted on August 9, 2005
Revised on April 18, 2006
Accepted on April 21, 2006


*Swammerdam Institute for Life Sciences, BioCentrum Amsterdam, University of Amsterdam, 1018 WV Amsterdam, The Netherlands;
Department of Biology and
Program in Molecular Biology and Biotechnology, University of North Carolina, Chapel Hill, NC 27599
Monitoring Editor: Anthony Bretscher
The yeast cell wall is an essential organelle that protects the cell from mechanical damage and antimicrobial peptides, participates in cell recognition and adhesion, and is important for the generation and maintenance of normal cell shape. We studied the localization of three covalently bound cell-wall proteins in S. cerevisiae. Tip1p was found only in mother cells, whereas Cwp2p was incorporated in small to medium-sized buds. When the promoter regions of TIP1 and CWP2 (responsible for transcription in early G1 and S/G2 phases, respectively) were exchanged, the localization patterns of Tip1p and Cwp2p were reversed, indicating that the localization of cell-wall proteins can be completely determined by the timing of transcription during the cell cycle. The third protein, Cwp1p, was incorporated into the birth scar, where it remained for several generations. However, we could not detect any role of Cwp1p in strengthening the birth-scar wall, or any functional interaction with the proteins that mark the birth-scar pole as a potential future budding site. Promoter-exchange experiments showed that expression in S/G2 phase is necessary but not sufficient for the normal localization of Cwp1p. Studies of mutants in which septum formation is perturbed indicate that the normal asymmetric localization of Cwp1p also depends on the normal timing of septum formation, composition of the septum, or both.