Abstract
We have combined and compared three techniques for predicting functional interactions based on comparative genomics (methods based on conserved operons, protein fusions and correlated evolution) and optimized these methods to predict coregulated sets of genes in 24 complete genomes, including Saccharomyces cerevisiae, Caenorhabditis elegans and 22 prokaryotes. The method based on conserved operons was the most useful for this purpose. Upstream regions of the genes comprising these predicted regulons were then used to search for regulatory motifs in 22 prokaryotic genomes using the motif-discovery program AlignACE. Many significant upstream motifs, including five known Escherichia coli regulatory motifs, were identified in this manner. The presence of a significant regulatory motif was used to refine the members of the predicted regulons to generate a final set of predicted regulons that share significant regulatory elements.
MeSH Terms
Animals
Base Sequence
Caenorhabditis elegans/genetics,metabolism
Computational Biology
Databases, Factual
Escherichia coli/genetics,metabolism
Genes/genetics
Genome
Phylogeny
Prokaryotic Cells/metabolism
Regulatory Sequences, Nucleic Acid/genetics
Regulon/genetics
Saccharomyces cerevisiae/genetics,metabolism
Sequence Alignment
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Manson McGuire A
Department of Genetics, Warren Alpert Building, Room 513, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Church G M
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