Evaluation of DNA methylation at imprinted DMRs in the spermatozoa of oligozoospermic men in association with MTHFR C677T genotype. (1st July 2016)

• Record Type: Journal Article
• Authors: Louie, K.; Minor, A.; Ng, R.; Poon, K.; Chow, V.; Ma, S.
• Is Part Of: Andrology. Volume 4:Number 5(2016:Sep.)
• Page Start: 825
• Page End: 831
• Publication Date: 2016-07-01
• Subjects: DNA methylation -- infertility -- single nucleotide polymorphism -- sperm concentration -- sperm quality; Andrology -- Periodicals; 616.65
• DOI: 10.1111/andr.12240
• Languages: English
• ISSNs: 2047-2919

Abstract

Summary: Altered DNA methylation has been previously identified in the spermatozoa of infertile men; however, the origins of these errors are poorly understood. DNA methylation is an epigenetic modification which is thought to play a fundamental role in male germline development. DNA methylation reactions rely on the cellular availability of methyl donors, which are primarily products of folate metabolism, where a key enzyme is methylenetetrahydrofolate reductase (MTHFR). The MTHFR C677T single nucleotide polymorphism (SNP) reduces enzyme activity and may potentially alter DNA methylation processes during germline development. The objective of this study was to determine whether altered DNA methylation in spermatozoa is associated with the MTHFR C677T SNP. DNA methylation was evaluated at the H19, IG‐GTL2, and MEST imprinted differentially methylated regions in the spermatozoa of 53 men – 44 oligozoospermic men and nine fertile men with normal sperm parameters via bisulfite sequencing of sperm clones. The 44 infertile men were stratified by severity of oligozoospermia – three normal (>15 million spermatozoa/mL), eight moderate (5–15 million spermatozoa/mL), 23 severe (1–5 million spermatozoa/mL), and 10 very severe (<1 million spermatozoa/mL). MTHFR C677T SNP genotyping was conducted in a subset of 44 peripheral blood samples via restriction fragment length polymorphism. A total of three men – severe oligozoospermic and CT genotype – were found to be altered, which is defined as having ≥50% of their clones altered, where an altered clone was in turn defined as ≥50% of CpGs with incorrect DNA methylation patterns. The incidence of three altered men within the CT subgroup, however, was not significantly higher than the incidence in the CC subgroup. Taken together, altered DNA methylation in spermatozoa was not significantly associated with the MTHFR C677T SNP; however, there was a trend for higher incidence of alterations among severe oligozoospermic infertile men with CT genotypes.