Bioinformatics Vol. 17 no. 7 2001
Pages 622-633
© 2001 Oxford University Press
Conformational model for binding site recognition by the E.coli MetJ transcription factor
Center for Computational Biology and Department of Genetics, Washington University School of Medicine, 700 S. Euclid Ave, St Louis, MO 63110, USA
Received on June 1, 2000
; revised on February 27, 2001
; accepted on March 4, 2001
Motivation: Current methods for identifying sequence specific binding sites in DNA sequence using position specific weight matrices are limited in both sensitivity and specificity. Double strand DNA helix exhibits sequence dependent variations in conformation. Interactions between macromolecules result from complementarity of the two tertiary structures. We hypothesize that this conformational variation plays a role in transcription factor binding site recognition, and that the use of this structure information will improve the predictive power of transcription factor binding site models.
Results: Conformation models for the sequence dependence of DNA helix distortion have been developed. Using our conformational models, we defined a tertiary structure template for the met operon repressor MetJ binding site. Both naturally occurring sites and precursor binding sites identified through in vitro selection were used as the basis for template definition. The conformational model appears to recognize features of protein binding sites that are distinct from the features recognized by primary sequence based profiles. Combining the conformational model and primary sequence profile yields a hybrid model with improved discriminatory power compared with either the conformational model or sequence profile alone. Using our hybrid model, we searched the E.coli genome. We are able to identify the documented MetJ sites in the promoter regions of metA, metB, metC, metR and metF. In addition, we find several novel loci with characteristics suggesting that they are functional MetJ repressor binding sites. Novel MetJ binding sites are found upstream of the metK gene, as well as upstream of a gene, abc, a gene that encodes for a component of a multifunction transporter which may transport amino acids across the membrane. The false positive rate is significantly lower than the sequence profile method.
Availability: The programs of implementation of this algorithm are available upon request. The list of crystal structures used for compiling the mean base step parameters of DNA is available by anonymous ftp at http://stateslab.wustl.edu/pub/helix/StructureList.
Contact: states{at}ccb.wustl.edu
* To whom correspondence should be addressed.
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