Functional sites of the Ada regulatory protein of Escherichia coli. Analysis by amino acid substitutions

Kyoko Takano, Yusaku Nakabeppu, Mutsuo Sekiguchi

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Specific cysteine residues at possible methyl acceptor sites of the Ada protein of Escherichia coli were converted to other amino acids by site-directed mutagenesis of the cloned ada gene of E. coli. Ada protein with the cysteine residue at 321 replaced by alanine was capable of accepting the methyl group from the methylphosphotriester but not from O6-methylguanine or O4-methylthymine of alkylated DNA, whereas the protein with alanine at position 69 accepted the methyl group from the methylated bases but not from the methylphosphotriester. These two mutants were used to elucidate the biological significance of repair of the two types of alkylation lesions. Introduction of the ada gene with the Ala69 mutation into an ada- cell rendered the cell more resistant to alkylating agents with respect to both killing and induction of mutations, but the gene with the Ala321 mutation exhibited no such activity. Replacement of the cysteine residue at position 69, but not at position 321, abolished the ability of Ada protein to promote transcription of both ada and alkA genes in vitro. These results are compatible with the idea that methylation of the cysteine residue at position 69 renders Ada protein active as a transcriptional regulator, whilst the cysteine residue at position 321 is responsible for repair of pre-mutagenic and lethal lesions in DNA. The actions of mutant Ada proteins on the ada and alkA promoters in vivo were investigated using an artificially composed gene expression system. When the ada gene with the Ala69 mutation was introduced into the cell, there was little induction of expression of either the ada or the alkA genes, even after treatment with an alkylating agent, in agreement with the data obtained from studies in vitro. With the Ala321 mutation, however, a considerable degree of ada gene expression occurred without adaptive treatment. The latter finding suggests that the cysteine residue at position 321, which is located near the C terminus of the Ada protein, is involved in regulating activity, as the transcriptional activator.

Original languageEnglish
Pages (from-to)261-271
Number of pages11
JournalJournal of Molecular Biology
Volume201
Issue number2
DOIs
Publication statusPublished - May 20 1988

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Escherichia coli Proteins
Amino Acid Substitution
Cysteine
Mutation
Genes
Alkylating Agents
Proteins
Alanine
Gene Expression
DNA
Alkylation
Mutant Proteins
Site-Directed Mutagenesis
Methylation
Escherichia coli
Amino Acids

All Science Journal Classification (ASJC) codes

  • Molecular Biology

Cite this

Functional sites of the Ada regulatory protein of Escherichia coli. Analysis by amino acid substitutions. / Takano, Kyoko; Nakabeppu, Yusaku; Sekiguchi, Mutsuo.

In: Journal of Molecular Biology, Vol. 201, No. 2, 20.05.1988, p. 261-271.

Research output: Contribution to journalArticle

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