DNA methylation changes between relapse and remission of minimal change nephrotic syndrome

Pediatr Nephrol. 2012 Dec;27(12):2233-41. doi: 10.1007/s00467-012-2248-z. Epub 2012 Aug 2.


Background: DNA methylation of gene promoters is associated with transcriptional inactivation. Changes in DNA methylation can lead to differences in gene expression levels and thereby influence disease development. We hypothesized that epigenetics underlies the pathogenesis of minimal change nephrotic syndrome (MCNS).

Methods: Genome-wide DNA methylation changes between relapse and remission in monocytes (n = 6) and naive T helper cells (Th0s) (n = 4) isolated from patients with MCNS were investigated using the microarray-based integrated analysis of methylation by isochizomers (MIAMI) method. We confirmed the MIAMI results using bisulfite-pyrosequencing analysis. Expression analysis was performed using quantitative real-time PCR.

Results: Three gene loci (GATA2, PBX4, and NYX) were significantly less methylated in Th0s during relapse than in remission, compared to none in monocytes. In addition, the distance distribution from the regression line of all probes in MIAMI was significantly different between monocytes and Th0s. The mRNA levels of the three genes in Th0s were not significantly different between relapse and remission.

Conclusions: Our results demonstrate that the change in DNA methylation patterns from remission to relapse in MCNS occurs predominantly in Th0s rather than in monocytes and suggest that epigenetic regulation in Th0s underlies the pathogenesis of MCNS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Child, Preschool
  • DNA Methylation / genetics*
  • Epigenesis, Genetic*
  • Female
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Monocytes / metabolism
  • Nephrosis, Lipoid / genetics*
  • Nephrosis, Lipoid / metabolism
  • Nephrotic Syndrome / genetics*
  • Nephrotic Syndrome / metabolism
  • Real-Time Polymerase Chain Reaction
  • Recurrence
  • Remission, Spontaneous
  • Sequence Analysis, DNA
  • T-Lymphocytes, Helper-Inducer / metabolism*