Human Molecular Genetics, Vol 6, 2243-2246, Copyright © 1997 by Oxford University Press
K Mitsuya, H Sui, M Meguro, H Kugoh, Y Jinno, N Niikawa and M Oshimura
The Wilms' tumor suppressor gene ( WT1 ) was previously identified as being
imprinted, with frequent maternal expression in human placentae and fetal
brains. We examined the allele-specific expression of WT1 in cultured human
fibroblasts from 15 individuals. Seven of 15 fibroblast lines were
heterozygous for polymorphic alleles, and the expression patterns were
variable, i.e., equal, unequal or monoallelic paternal expression in three,
two and two cases, respectively. Exclusive paternal expression of WT1 was
also shown in non-cultured peripheral lymphocytes from the latter two
individuals. The allele-specific expression profiles of other imprinted
genes, IGF2 and H19, on human chromosome 11 were constant and consistent
with those in other tissues. Our unexpected observations of paternal or
biallelic expression of WT1 in fibroblasts and lymphocytes, together with
the previous findings of maternal or biallelic expression in placentae and
brains, suggest that the allele-specific regulatory system of WT1 is unique
and may be controlled by a putative tissue- and individual-specific
modifier.
ARTICLES
Paternal expression of WT1 in human fibroblasts and lymphocytes
Department of Molecular and Cell Genetics, School of Life Sciences, Faculty of Medicine, Tottori University, Nishimachi 86, Yonago, Tottori 683, Japan.
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