Endocrine Abstracts

Genomic imprinting is an epigenetic mechanism by which a subset of our genes displays unequal expression of the maternal and paternal alleles; in many cases, one allele is fully silenced. It occurs because these genes are marked differently (by DNA methylation and/or histone modifications) in male and female gametes. These gamete-specific marks are maintained at fertilisation and perpetuated throughout development and adult life, such that the alleles of imprinted genes retain...