Global Transcriptional Responses of Fission Yeast to Environmental Stress
Abstract
We explored transcriptional responses of the fission yeast Schizosaccharomyces pombe to various environmental stresses. DNA microarrays were used to characterize changes in expression profiles of all known and predicted genes in response to five stress conditions: oxidative stress caused by hydrogen peroxide, heavy metal stress caused by cadmium, heat shock caused by temperature increase to 39°C, osmotic stress caused by sorbitol, and DNA damage caused by the alkylating agent methylmethane sulfonate. We define a core environmental stress response (CESR) common to all, or most, stresses. There was a substantial overlap between CESR genes of fission yeast and the genes of budding yeast that are stereotypically regulated during stress. CESR genes were controlled primarily by the stress-activated mitogen-activated protein kinase Sty1p and the transcription factor Atf1p. S. pombe also activated gene expression programs more specialized for a given stress or a subset of stresses. In general, these “stress-specific” responses were less dependent on the Sty1p mitogen-activated protein kinase pathway and may involve specific regulatory factors. Promoter motifs associated with some of the groups of coregulated genes were identified. We compare and contrast global regulation of stress genes in fission and budding yeasts and discuss evolutionary implications.
Annotations for Table Table11 are from GeneDB at http://www.genedb.org/genedb/pombe/index.jsp, some of them being edited by hand. Fifty-two additional proteins with no known function are not listed here (see our website for complete gene list).
For details on data and gene lists, see MATERIALS AND METHODS. N in the patterns means either A, C, G, or T; K means G or T; and Y means C or T.
ACKNOWLEDGMENTS
We thank Val Wood for support with gene annotations and information on orphans and orthologs, Dave Vetrie for microarray printing, Jaak Vilo for help with SPEXS software, Audrey Gasch and Helen Causton for critical reading of the manuscript, Helen Parkinson and Rob Andrews for help with preparing data for ArrayExpress, Jonathan Millar for a sty1Δ strain, Roger Pettet for development of the gene expression views, and the developers of GeneDB for providing this useful database. We apologize to colleagues in the field for not citing all relevant papers due to space limitations. D.C. and W.M.T. were supported by the EMF Biological Research Trust. This research was funded by Cancer Research UK (Jones and Bähler laboratories), and A.B. was partly funded by the TEMBLOR grant from the European Commission.
Footnotes
Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E02–08–0499. Article and publication date are at www.molbiolcell.org/cgi/doi/10.1091/mbc.E02–08–0499.






