We have investigated the potential role of DNA methylation as a regula
tor of imprinted Xist expression in mouse preimplantation embryos. The
active paternal allele was found to be unmodified in sperm at CpG loc
i near the 5' end of the gene transcription unit. In contrast, on the
inactive maternal allele, these same sites are initially methylated in
the oocyte and then remain modified in the early embryo. In the male
germ line, these methyl moieties are removed during spermatogenesis, a
nd this occurs before the programmed reactivation of Xist in the testi
s. This represents a clear-cut example of a potential methylation impr
inting signal that is reprogrammable and gamete derived.