Abstract

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 (meAda) is able to bind a DNA sequence between 40 and 60 base pairs upstream of the aidB transcriptional startpoint. Binding of meAda is necessary to activate transcription of the adaptive response genes; accordingly, in vitro transcription of aidB is dependent on the presence of meAda. Unmethylated Ada protein shows no protection against DNaseI digestion in the aidB promoter region nor does it promote aidB in 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 meAda might be AATnnnnnnG-CAA. 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.

Highlights

  • Genes belonging to the adaptive response are positively regulated by the ada gene; the Ada protein acts as a transcriptional actio vator when methylated in one of its cysteine residues at position 69

  • Through DNaseI protection assays, we show that methylated Ada is able to bind a DNA sequence between 40 and 60 base pairs upstream of the aidB transcriptional startpoint

  • Based on the comparison of five different Adadependent promoter regions, we suggest that a possible recognition sequence for methylated at Cys-69 (meAda) might be AATnnnnnnGCAA

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Summary

THE JOURNAL OF BIOLOGICAL CHEMISTRY

Vol 270, No 14, Issue of April 7, pp. 8285-8289, 1995 Printed in U.S.A. (Received for publication, December 12, 1994, and in revised form, February 7, 1995). Ada protein methylated at Cys-69 (meAda) can bind to specific DNA sequences in the promoter region of several genes; binding of meAda makes the promoters accessible to RNA polymerase and activates their transcription (3, 4). It seems possible that the AidB protein is involved in a detoxification pathway for MNNG, it is still unclear if this function is related to its isovaleryl-coenzyme A dehydrogenase activity For both the ada/alkB and the alkA promoters, the Adabinding site has been determined by DNaseI protection experiments; two short sequences common to both ada and alkA promoter regions (AAANNAA and AAAGCGCA) have been proposed as the Ada-binding sequence (Ada box) by different papers

ATG GAG GGA GAC ACA GTGC
MATERIALS AND METHODS
RESULTS
Ada meAda
DIS CUSSI ON
REFE RENCES
Full Text
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