Role of DNA minor groove interactions in substrate recognition by the M.Sinl and M.EcoRII DNA (cytosine-5) methyltransferases

A. Kiss, G. Pósfai, Gábor Zsurka, Tamás Raskó, Pál Venetianer

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

The Sin1 and EcoRII DNA methyltransferases recognize sequences (GGA/TCC and CCA/TGG, respectively), which are characterized by an A/T ambiguity. Recognition of the A·T and T·A base pair was studied by in vitro methyltransferase assays using oligonucleotide substrates containing a hypoxanthine·C base pair in the central position of the recognition sequence. Both enzymes methylated the substituted oligonucleotide with an efficiency that was comparable to methylation of the canonical substrate. These observations indicate that M.Sin1 and M.EcoRII discriminate between their canonical recognition site and the site containing a G·C or a C·G base pair in the center of the recognition sequence (GGG/CCC and CCG/CGG, respectively) by interaction(s) in the DNA minor groove. M.Sinl mutants displaying a decreased capacity to discriminate between the GGA/TCC and GGG/CCC sequences were isolated by random mutagenesis and selection for the relaxed specificity phenotype. These mutations led to amino acid substitutions outside the variable region, previously thought to be the sole determinant of sequence specificity. These observations indicate that A/T versus G/C discrimination is mediated by interactions between the large domain of the methyltransferase and the minor groove surface of the DNA.

Original languageEnglish
Pages (from-to)3188-3194
Number of pages7
JournalNucleic Acids Research
Volume29
Issue number15
Publication statusPublished - Aug 1 2001

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DNA (Cytosine-5-)-Methyltransferase
Base Pairing
Methyltransferases
Oligonucleotides
DNA
Amino Acid Substitution
Mutagenesis
Methylation
Phenotype
Mutation
Enzymes

ASJC Scopus subject areas

  • Genetics

Cite this

Role of DNA minor groove interactions in substrate recognition by the M.Sinl and M.EcoRII DNA (cytosine-5) methyltransferases. / Kiss, A.; Pósfai, G.; Zsurka, Gábor; Raskó, Tamás; Venetianer, Pál.

In: Nucleic Acids Research, Vol. 29, No. 15, 01.08.2001, p. 3188-3194.

Research output: Contribution to journalArticle

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