Moderate folate deficiency does not cause global hypomethylation of hepatic and colonic DNA or c-myc-specific hypomethylation of colonic DNA in rats

Am J Clin Nutr. 1995 May;61(5):1083-90. doi: 10.1093/ajcn/61.4.1083.

Abstract

Global and gene-specific DNA hypomethylation is considered to be an important early epigenetic event in several human neoplasms. A growing body of evidence has suggested that DNA methylation can be altered by dietary manipulation of methyl group donors. This study investigated whether moderate depletion of folate, a dietary component needed for the synthesis of methyl groups, would cause decreased hepatic and colonic S-adenosylmethionine concentrations, and thereby lead to global and/or protooncogene-specific DNA hypomethylation. Weanling rats were fed an amino acid-defined diet containing either 0 or 8 mg folate/kg diet for 15 or 24 wk. Significantly lower systemic, hepatic and colonic folate concentrations were observed in the moderately folate-depleted rats than in controls at both 15 and 24 wk (P < 0.005). Although hepatic S-adenosylmethionine was significantly lower in the moderately folate-depleted rats than in controls at the two time points (P < 0.03), colonic S-adenosylmethionine concentrations were not significantly different between the two groups at either time point. No significant differences between the folate-depleted and control animals could be detected with regard to global DNA methylation in the liver or colonic mucosa. Furthermore, c-myc protooncogene-specific DNA methylation in the colonic mucosa was not significantly different between these two groups of animals. These results indicate that moderate folate depletion does not cause a significant reduction in global DNA methylation in liver or colonic mucosa or in c-myc-specific colonic mucosal DNA methylation in this rat model.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Body Weight
  • Colon / chemistry*
  • Colon / metabolism
  • Colorectal Neoplasms / etiology
  • Colorectal Neoplasms / genetics
  • DNA / analysis
  • DNA / metabolism*
  • Folic Acid / pharmacology
  • Folic Acid Deficiency / metabolism*
  • Folic Acid Deficiency / physiopathology
  • Gene Expression Regulation, Neoplastic
  • Genes, myc / genetics*
  • Liver / chemistry*
  • Liver / metabolism
  • Male
  • Methionine / metabolism
  • Methylation
  • Proto-Oncogene Proteins c-myc / genetics
  • Proto-Oncogene Proteins c-myc / metabolism
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • S-Adenosylmethionine / analysis
  • S-Adenosylmethionine / metabolism

Substances

  • Proto-Oncogene Proteins c-myc
  • S-Adenosylmethionine
  • DNA
  • Folic Acid
  • Methionine