Though DNA methylation is necessary to maintain monoallelic expression of i
mprinted genes, it is still unclear whether it represents the primary mark.
Here we ask whether the imprinting mark is still present in terminally dif
ferentiated somatic cells in which the transcription of embryo-specific imp
rinted genes was shut off. For such analysis H19 and Igf2 genes were activa
ted by inducing differentiation of (mouse embryonal carcinoma cell x mouse
lymphocyte) hybrid cell clones. Although lymphocytes do not express H19 and
Igf2, both genes are reactivated in a proper monoallelic manner in hybrid
cells. Analysis of the up-stream region of the R19 gene confirmed maintenan
ce of differential methylation of the active and inactive H19 genes of lymp
hocyte origin, although a tendency toward in vitro induced hypermethylation
was apparent. We conclude that the imprints of the H19, U2af1-rs1, and Igf
2 genes are maintained in lymphocytes in adult mice. (C) 1999 Academic Pres
s.