TY - JOUR
T1 - H19 IS IMPRINTED IN THE CHOROID-PLEXUS AND LEPTOMENINGES OF THE MOUSE FETUS
AU - SVENSSON, K
AU - Walsh, Colum
AU - FUNDELE, R
AU - OHLSSON, R
PY - 1995/5
Y1 - 1995/5
N2 - It has been proposed that either the Igf-2 gene or the H19 gene - but not both - can be expressed from a given chromosome. Igf-2 is known to be biallelically expressed in the choroid plexus and leptomeninges, however, raising the question of whether H19 is down-regulated or absent there. We found by in situ hybridization that H19 is indeed expressed in the choroid plexus and leptomeninges of the developing mouse foetus. Comparison with the expression pattern of Igf-2 showed that the genes are coexpressed in all areas, with the exception of the choroid plexus epithelium. To evaluate whether H19 is also biallelically expressed in these tissues, we microdissected embryos from interspecific crosses and performed RNAse protection analysis on the isolated RNA. This revealed that H19 maintains its imprint in the choroid plexus/leptomeninges, being transcribed from the maternal allele at a level comparable to that in normal liver. We discuss the significance of these results for current models of Igf-2 and H19 imprinting.
AB - It has been proposed that either the Igf-2 gene or the H19 gene - but not both - can be expressed from a given chromosome. Igf-2 is known to be biallelically expressed in the choroid plexus and leptomeninges, however, raising the question of whether H19 is down-regulated or absent there. We found by in situ hybridization that H19 is indeed expressed in the choroid plexus and leptomeninges of the developing mouse foetus. Comparison with the expression pattern of Igf-2 showed that the genes are coexpressed in all areas, with the exception of the choroid plexus epithelium. To evaluate whether H19 is also biallelically expressed in these tissues, we microdissected embryos from interspecific crosses and performed RNAse protection analysis on the isolated RNA. This revealed that H19 maintains its imprint in the choroid plexus/leptomeninges, being transcribed from the maternal allele at a level comparable to that in normal liver. We discuss the significance of these results for current models of Igf-2 and H19 imprinting.
U2 - 10.1016/0925-4773(94)00345-N
DO - 10.1016/0925-4773(94)00345-N
M3 - Article
SN - 1872-6356
VL - 51
SP - 31
EP - 37
JO - Mechanisms of Development
JF - Mechanisms of Development
IS - 1
ER -