Copyright © 1998 Cell Press. All rights reserved.
, Vol 2, 65-73, July 1998

Article

A Genome-Wide Transcriptional Analysis of the Mitotic Cell Cycle

Raymond J. Cho,1 Michael J. Campbell,2 Elizabeth A. Winzeler,2 Lars Steinmetz,1 Andrew Conway,2 Lisa Wodicka,3 Tyra G. Wolfsberg,4 Andrei E. Gabrielian,4 David Landsman,4 David J. Lockhart,3 and Ronald W. Davis

1Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA

2Department of Biochemistry, Stanford University School of Medicine, Stanford, California 94305, USA

3Affymetrix, 3380 Central Expressway, Santa Clara, California 95051, USA

4National Center for Biotechnology Information, National Library of Medicine, Bethesda, Maryland 20894, USA

u2217Corresponding author
Michael J. Campbell
650 723 6161 (phone)
650 723 6783 (fax)
campbell@cmgm.stanford.edu


Summary


Progression through the eukaryotic cell cycle is known to be both regulated and accompanied by periodic fluctuation in the expression levels of numerous genes. We report here the genome-wide characterization of mRNA transcript levels during the cell cycle of the budding yeast S. cerevisiae. Cell cycle–dependent periodicity was found for 416 of the 6220 monitored transcripts. More than 25% of the 416 genes were found directly adjacent to other genes in the genome that displayed induction in the same cell cycle phase, suggesting a mechanism for local chromosomal organization in global mRNA regulation. More than 60% of the characterized genes that displayed mRNA fluctuation have already been implicated in cell cycle period-specific biological roles. Because more than 20% of human proteins display significant homology to yeast proteins, these results also link a range of human genes to cell cycle period-specific biological functions.

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