| Literature DB >> 18425848 |
Geng Tian1, Umashankar Singh, Yang Yu, Buffy S Ellsworth, Myriam Hemberger, Rudolf Geyer, M David Stewart, Richard R Behringer, Reinald Fundele.
Abstract
The LIM homeobox containing genes of the LIM-3 group, Lhx3 and Lhx4, are critical for normal development. Both genes are involved in the formation of the pituitary and the motoneuron system and loss of either gene causes perinatal lethality. Previous studies had shown that Lhx3 is overexpressed in hyperplastic placentas of mouse interspecies hybrids. To determine the role of LHX3 in the mouse placenta, we performed expression and function analyses. Our results show that Lhx3 exhibits specific spatial and temporal expression in the mouse placenta. However, deletion of Lhx3 does not produce a placental phenotype. To test whether this is due to functional substitution by Lhx4, we performed a phenotype analysis of Lhx3-/-; Lhx4-/- double-mutant placentas. A subset of Lhx3-/-; Lhx4-/- placentas exhibited abnormal structure of the labyrinth. However, absence of both LIM-3 genes did not interfere with placental transport nor consistently with expression of target genes such as Gnrhr. Thus, LHX3 and LHX4 appear to be dispensable for placental development and function.Entities:
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Year: 2008 PMID: 18425848 PMCID: PMC3632286 DOI: 10.1002/dvdy.21546
Source DB: PubMed Journal: Dev Dyn ISSN: 1058-8388 Impact factor: 3.780