Transcription factors NF-YA regulate the induction of human OGG1 following DNA-alkylating agent methylmethane sulfonate (MMS) treatment

J Biol Chem. 2004 Mar 12;279(11):9857-66. doi: 10.1074/jbc.M311132200. Epub 2003 Dec 19.

Abstract

A human 8-oxoguanine-DNA glycosylase (hOGG1) is the main enzyme that repairs 8-oxoG, which is a critical mutagenic lesion. There is a great deal of interest in the up- or down-regulation of OGG1 expression after DNA damage. In this study, we investigated the effect of a DNA-alkylating agent, methylmethane sulfonate (MMS), on hOGG1 expression level and found that MMS treatment resulted in an increase in the functional hOGG1 expression in HCT116 cells. A region between -121 and -61 of the hOGG1 promoter was found to be crucial for this induction by MMS. Site-directed mutations of the two inverted CCAAT motifs substantially abrogated the induction of the hOGG1 promoter as a result of MMS treatment. In addition, the NF-YA protein (binding to the inverted CCAAT box) was induced after exposing cells to MMS. Moreover, gel shift and supershift analyses with the nuclear extracts prepared from HCT116 cells identified NF-YA as the transcription factor interacting with the inverted CCAAT box. Mutations of the inverted CCAAT box either prevented the binding of this factor or abolished its activation as a result of MMS treatment. Finally, this study showed that hOGG1-expressing HCT116 cells exhibited increased hOGG1 repair activity and resistance to MMS. Overall, these results demonstrate that MMS can up-regulate hOGG1 expression through the induction of the transcription factor, NF-YA, and increased transcription level of the hOGG1 gene correlates with an increase in enzyme activity providing functional protection from MMS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / pharmacology
  • Alkylating Agents / pharmacology*
  • Amino Acid Motifs
  • Antineoplastic Agents, Alkylating / pharmacology
  • Blotting, Western
  • CCAAT-Binding Factor / metabolism
  • CCAAT-Binding Factor / physiology*
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Cell Survival
  • DNA / chemistry*
  • DNA Glycosylases / metabolism*
  • DNA Repair
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation, Neoplastic
  • Guanine / analogs & derivatives
  • Guanine / chemistry
  • Guanosine / analogs & derivatives*
  • Guanosine / metabolism
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Luciferases / metabolism
  • Methyl Methanesulfonate / pharmacology*
  • Mutagenesis, Site-Directed
  • Mutation
  • Plasmids / metabolism
  • Protein Binding
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Transfection
  • Up-Regulation

Substances

  • Adjuvants, Immunologic
  • Alkylating Agents
  • Antineoplastic Agents, Alkylating
  • CCAAT-Binding Factor
  • NFYA protein, human
  • Transcription Factors
  • Guanosine
  • 8-hydroxyguanosine
  • Guanine
  • 7-methylguanine
  • DNA
  • Methyl Methanesulfonate
  • Hydrogen Peroxide
  • Luciferases
  • DNA Glycosylases
  • oxoguanine glycosylase 1, human