Epigenetic modifications at DMRs of imprinting genes in sperm of type 2 diabetic men

Zygote. 2022 Oct;30(5):638-647. doi: 10.1017/S0967199422000107. Epub 2022 May 23.

Abstract

High rates of infertility in type 2 diabetic (T2DM) men have led to attempts to understand the mechanisms involved in this process. This condition can be investigated from at least two aspects, namely sperm quality indices and epigenetic alterations. Epigenetics science encompasses the phenomena that can lead to inherited changes independently of the genetics. This study has been performed to test the hypothesis of the relationship between T2DM and the epigenetic profile of the sperm, as well as sperm quality indices. This research included 42 individuals referred to the infertility clinic of Royan Institute, Iran in 2019-2021. The study subjects were assigned to three groups: normozoospermic non-diabetic (control), normozoospermic diabetic (DN) and non-normozoospermic diabetic (D.Non-N). Sperm DNA fragmentation was evaluated using the sperm chromatin structure assay technique. The global methylation level was examined using 5-methyl cytosine antibody and the methylation status in differentially methylated regions of H19, MEST, and SNRPN was assessed using the methylation-sensitive high-resolution melting technique. The results showed that the sperm global methylation in spermatozoa of D.Non-N group was significantly reduced compared with the other two groups (P < 0.05). The MEST and H19 genes were hypomethylated in the spermatozoa of D.Non-N individuals, but the difference level was not significant for MEST. The SNRPN gene was significantly hypermethylated in these individuals (P < 0.05). The results of this study suggest that T2DM alters the methylation profile and epigenetic programming in spermatozoa of humans and that these methylation changes may ultimately influence the fertility status of men with diabetes.

Keywords: DNA methylation; Diabetes mellitus; Epigenetics processes; Genomic imprinting; Spermatozoa.

MeSH terms

  • Chromatin / metabolism
  • Cytosine / metabolism
  • DNA Methylation
  • Diabetes Mellitus, Type 2* / genetics
  • Diabetes Mellitus, Type 2* / metabolism
  • Genomic Imprinting*
  • Humans
  • Male
  • Semen / metabolism
  • Spermatozoa / metabolism
  • snRNP Core Proteins / genetics
  • snRNP Core Proteins / metabolism

Substances

  • Chromatin
  • snRNP Core Proteins
  • Cytosine