Mouse Chromosome (Chr) 7 distal to band F3 on the physical map is know
n to be subject to imprinting, maternal duplication (MatDp) of the reg
ion leading to a late embryonic lethality, while paternal duplication
(PatDp) causes death in utero before 11.5 dpc. Using a new mouse recip
rocal translocation T(7;11)65H to produce MatDp for distal Chr 7, we h
ave mapped the region subject to imprinting more precisely to bands 7F
4/F5 on the cytogenetic map. Fluorescence in situ hybridization (FISH)
studies on mitotic and meiotic chromosomes of a T65H heterozygote sho
w that the imprinted gene Igf2 is located in the same region. This was
confirmed by the finding that embryos with MatDp of bands 7F4/F5 did
not express Igf2. We suggest that other members of the imprinted domai
n containing Igf2, namely Mash2, H19, Ins2, and p57(K1P2), also locate
d in 7F4/F5 and that some or all of these genes may be responsible for
the two imprinting lethalities seen with MatDp and PatDp for this reg
ion.