Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction.

ABSTRACT: Several imprinted genes have been implicated in the regulation of placental function and embryonic growth. On distal mouse chromosome 7, two clusters of imprinted genes, each regulated by its own imprinting center (IC), are separated by a poorly characterized region of 280kb (the IC1-IC2 interval). We previously generated a mouse line in which this IC1-IC2 interval has been deleted (Del(7AI) allele) and found that maternal inheritance of this allele results in low birth weights in newborns. Here we report that Del(7AI) causes a partial loss of Ascl2, a maternally expressed gene in the IC2 cluster, which when knocked out leads to embryonic lethality at midgestation due to a lack of spongiotrophoblast formation. The hypomorphic Ascl2 allele causes embryonic growth restriction and an associat

SUBMITTER: Oh-McGinnis R 

PROVIDER: S-EPMC3820550 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature