The use of high density DNA arrays to monitor gene expression at a genome-w
ide scale constitutes a fundamental advance in biology. In particular, the
expression pattern of all genes in Saccharomyces cerevisiae can be interrog
ated using microarray analysis where cDNAs are hybridized to an array of mo
re than 6000 genes in the yeast genome. In an effort to build a comprehensi
ve Yeast Promoter Database and to develop new computational methods for map
ping upstream regulatory elements, we started recently in an on going colla
boration with experimental biologists on analysis of large-scale expression
data. It is well known that complex gene expression patterns result from d
ynamic interacting networks of genes in the genetic regulatory circuitry. H
ierarchical and modular organization of regulatory DNA sequence elements ar
e important information for our understanding of combinatorial control of g
ene expression. As a bioinformatics attempt in this new direction, we have
done some computational exploration of various initial experimental data. W
e will use cell-cycle regulated gene expression as a specific example to de
monstrate how one may extract promoter information computationally from suc
h genome-wide screening. Full report of the experiments and of the complete
analysis will be published elsewhere when all the experiments are to be fi
nished later in this year (Spellman, P.T., et al. 1998. Mol. Biol. Cell 9,
3273-3297). (C) 1999 Elsevier Science Ltd. All rights reserved.