Global methylation status of sperm DNA in carriers of chromosome structural aberrations

Asian J Androl. 2017 Jan-Feb;19(1):117-124. doi: 10.4103/1008-682X.168684.

Abstract

Male infertility might be clearly associated with aberrant DNA methylation patterns in human spermatozoa. An association between oxidative stress and the global methylation status of the sperm genome has also been suggested. The aim of the present study was to determine whether the global sperm DNA methylation status was affected in the spermatozoa of carriers of chromosome structural aberrations. The relationships between the 5-methylcytosine (m 5 C) levels in spermatozoa and chromatin integrity status were evaluated. The study patients comprised male carriers of chromosome structural aberrations with reproductive failure (n = 24), and the controls comprised normozoospermic sperm volunteers (n = 23). The global m 5 C level was measured using thin-layer chromatography (TLC) and immunofluorescence (IF) techniques. The sperm chromatin integrity was assessed using aniline blue (AB) staining and TUNEL assay. The mean m 5 C levels were similar between the investigated chromosome structural aberrations carriers (P) and controls (K). However, sperm chromatin integrity tests revealed significantly higher values in chromosomal rearrangement carriers than in controls (P < 0.05). Although the potential relationship between sperm chromatin integrity status and sperm DNA fragmentation and the m 5 C level juxtaposed in both analyzed groups (P vs K) was represented in a clearly opposite manner, the low chromatin integrity might be associated with the high hypomethylation status of the sperm DNA observed in carriers of chromosome structural aberrations.

MeSH terms

  • 5-Methylcytosine / metabolism*
  • Adult
  • Case-Control Studies
  • Chromatin / metabolism*
  • Chromatography, Thin Layer
  • Chromosome Aberrations*
  • DNA Fragmentation*
  • DNA Methylation*
  • Fluorescent Antibody Technique
  • Gene Rearrangement
  • Humans
  • In Situ Nick-End Labeling
  • Infertility, Male / genetics*
  • Infertility, Male / metabolism
  • Male
  • Oxidative Stress
  • Spermatozoa / metabolism*
  • Translocation, Genetic

Substances

  • Chromatin
  • 5-Methylcytosine