| First Author | Aarabi M | Year | 2018 |
| Journal | Hum Mol Genet | Volume | 27 |
| Issue | 7 | Pages | 1123-1135 |
| PubMed ID | 29360980 | Mgi Jnum | J:260788 |
| Mgi Id | MGI:6150560 | Doi | 10.1093/hmg/ddy021 |
| Citation | Aarabi M, et al. (2018) Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementation. Hum Mol Genet 27(7):1123-1135 |
| abstractText | Supplementation with high doses of folic acid, an important mediator of one-carbon transfers for DNA methylation, is used clinically to improve sperm parameters in infertile men. We recently detected an unexpected loss of DNA methylation in the sperm of idiopathic infertile men after 6 months of daily supplementation with 5 mg folic acid (>10x the daily recommended intake-DRI), exacerbated in men homozygous for a common variant in the gene encoding an important enzyme in folate metabolism, methylenetetrahydrofolate reductase (MTHFR 677C>T). To investigate the epigenomic impact and mechanism underlying effects of folic acid on male germ cells, wild-type and heterozygote mice for a targeted inactivation of the Mthfr gene were fed high-dose folic acid (10x the DRI) or control diets (CDs) for 6 months. No changes were detected in general health, sperm counts or methylation of imprinted genes. Reduced representation bisulfite sequencing revealed sperm DNA hypomethylation in Mthfr+/- mice on the 10x diets. Wild-type mice demonstrated sperm hypomethylation only with a very high dose (20x) of folic acid for 12 months. Testicular MTHFR protein levels decreased significantly in wild-type mice on the 20x diet but not in those on the 10x diet, suggesting a possible role for MTHFR deficiency in sperm DNA hypomethylation. In-depth analysis of the folic acid-exposed sperm DNA methylome suggested mouse/human susceptibility of sequences with potential importance to germ cell and embryo development. Our data provide evidence for a similar cross-species response to high dose folic acid supplementation, of sperm DNA hypomethylation, and implicate MTHFR downregulation as a possible mechanism. |
