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(Received for publication, December 12, 1994; and in revised form, February 7, 1995) The Escherichia coli aidB gene is part of the adaptive
response to DNA methylation damage. Genes belonging to the adaptive
response are positively regulated by the ada gene; the Ada
protein acts as a transcriptional activator when methylated in one of
its cysteine residues at position 69. Through DNaseI protection assays,
we show that methylated Ada (
Volume 270,
Number 14,
Issue of April 7, 1995 pp. 8285-8289
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
EVIDENCE FOR A NEW CONSENSUS SEQUENCE FOR Ada-BINDING SITES
Ada) is able to bind a DNA
sequence between 40 and 60 base pairs upstream of the aidB transcriptional startpoint. Binding of
Ada is
necessary to activate transcription of the adaptive response genes;
accordingly, in vitro transcription of aidB is
dependent on the presence of
Ada. Unmethylated Ada protein
shows no protection against DNaseI digestion in the aidB promoter region nor does it promote aidBin vitro transcription. The aidB Ada-binding site shows only weak
homology to the proposed consensus sequences for Ada-binding sites in E. coli (AAANNAA and AAAGCGCA) but shares a higher degree of
similarity with the Ada-binding regions from other bacterial species,
such as Salmonella typhimurium and Bacillus subtilis.
Based on the comparison of five different Ada-dependent promoter
regions, we suggest that a possible recognition sequence for
Ada might be AATnnnnnnGCAA. Higher concentrations of Ada
are required for the binding of aidB than for the ada promoter, suggesting lower affinity of the protein for the aidB Ada-binding site. Common features in the Ada-binding
regions of ada and aidB are a high A/T content, the
presence of an inverted repeat structure, and their position relative
to the transcriptional start site. We propose that these elements, in
addition to the proposed recognition sequence, are important for
binding of the Ada protein.
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