Altered sperm DNA methylation in overweight men associates with transposable element regulation of paternal origins of risk in children

Abstract

The occurrence of childhood neurodevelopmental disorders has been steadily increasing for decades yet we have little understanding of modes of inheritance implicated in these diseases. Epidemiology studies have revealed an association between an elevated paternal BMI and an increased risk for autism in children, suggesting non-genetic modes of inheritance may be involved. Epigenetic marks, like DNA methylation at cytosines, are especially susceptible to environmental, diet and lifestyle changes. Yet, whether a mans BMI influences the sperm methylome and potentially impacts offspring development remains unresolved. Using MethylC capture (MCC)-sequencing, we identified over 38 000 differentially methylated CpGs (DMCs) in the sperm of men with an elevated BMI, with many occurring in regions that were enriched for neural gene and disease ontologies. Differentially methylated regions (DMRs) were enriched at transposable elements that can act as active enhancers during human zygotic genome activation, and at gene promoters for early lineage specification. These results suggest that sperm methylome alterations that are linked to an elevated BMI may influence key embryonic transcriptional process, notably those associated with trophectoderm and placental development.