Abstract
A short oligodeoxynucleotide (ODN) with 2-(1H)-pyrimidinone at the HhaI DNA methyltransferase target site (GCGC) is shown to induce a level of inhibition of methyl transfer and thermal stability of the complex with the enzyme identical to that achieved with a similar ODN substituted with 5-azacytosine. The drugs responsible for these effects-zebularine and 5-azacytidine/2'-deoxy-5-azacytidine-are contrasted in terms of chemical stability and possible metabolic activation by a brief structure-activity analysis.
MeSH terms
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Antineoplastic Agents / metabolism*
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Cytidine / analogs & derivatives
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Cytidine Deaminase / antagonists & inhibitors
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DNA (Cytosine-5-)-Methyltransferases / antagonists & inhibitors
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DNA / metabolism
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DNA-Cytosine Methylases / antagonists & inhibitors*
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Protein Structure, Tertiary
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Pyrimidine Nucleosides / metabolism*
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Pyrimidine Nucleosides
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Cytidine
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pyrimidin-2-one beta-ribofuranoside
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DNA
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DNA modification methylase HhaI
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DNA-Cytosine Methylases
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DNA (Cytosine-5-)-Methyltransferases
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Cytidine Deaminase