TY - JOUR
T1 - Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth
AU - Li, Yuanhao
AU - Behringer, Richard R.
N1 - Funding Information:
We thank A. Bradley for the AB-1 ES and SNL 76/7 STO cell lines, A. Nagy for the ploxPneo-1 plasmid, K. Mahon for probes, K. Dunner Jr and C. Bucana for TEM, and S. Glasser, R. Farnsworth and K. Mahon for helpful discussions. The M.D. Anderson Cancer Center High Resolution Electron Microscopy Facility is supported by an institutional core grant from the National Institutes of Health (NIH). This study was supported by NIH grant HD30284 to R.R.B.
PY - 1998
Y1 - 1998
N2 - In marsupials and mice, the paternally derived X chromosome is preferentially inactivated in the placental tissues of female embryos. We show here that the X-linked homeobox gene Esx1 (refs 5,6), whose expression is restricted to extraembryonic tissues, is a chromosomally imprinted regulator of placental morphogenesis and trophoblast differentiation. Heterozygous female mice that inherited a mutant Esx1 allele from their father developed normally. Heterozygous females that inherited the Esx1 mutation from their mother however, were born 20% smaller than normal and are identical in phenotype to hemizygous mutant males and homozygous mutant females. Although Esx1 mutant embryos were initially comparable in size with controls at 13.5 days post coitum (dpc), their placentas were significantly larger. Defects in the morphogenesis of the labyrinthine layer were observed as early as 11.5 dpc. Subsequently, vascularization abnormalities developed at the maternal-fetal interface, causing fetal growth retardation. These results identify Esx1 as the first essential X-chromosome-imprinted regulator of placental development that influences fetal growth, and may aid our understanding human placental insufficiency syndromes.
AB - In marsupials and mice, the paternally derived X chromosome is preferentially inactivated in the placental tissues of female embryos. We show here that the X-linked homeobox gene Esx1 (refs 5,6), whose expression is restricted to extraembryonic tissues, is a chromosomally imprinted regulator of placental morphogenesis and trophoblast differentiation. Heterozygous female mice that inherited a mutant Esx1 allele from their father developed normally. Heterozygous females that inherited the Esx1 mutation from their mother however, were born 20% smaller than normal and are identical in phenotype to hemizygous mutant males and homozygous mutant females. Although Esx1 mutant embryos were initially comparable in size with controls at 13.5 days post coitum (dpc), their placentas were significantly larger. Defects in the morphogenesis of the labyrinthine layer were observed as early as 11.5 dpc. Subsequently, vascularization abnormalities developed at the maternal-fetal interface, causing fetal growth retardation. These results identify Esx1 as the first essential X-chromosome-imprinted regulator of placental development that influences fetal growth, and may aid our understanding human placental insufficiency syndromes.
UR - http://www.scopus.com/inward/record.url?scp=0031765409&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031765409&partnerID=8YFLogxK
U2 - 10.1038/3129
DO - 10.1038/3129
M3 - Article
C2 - 9806555
AN - SCOPUS:0031765409
SN - 1061-4036
VL - 20
SP - 309
EP - 311
JO - Nature Genetics
JF - Nature Genetics
IS - 3
ER -