Pten regulates collective cell migration during specification of the anterior-posterior axis of the mouse embryo.
Ontology highlight
ABSTRACT: Pten, the potent tumor suppressor, is a lipid phosphatase that is best known as a regulator of cell proliferation and cell survival. Here we show that mouse embryos that lack Pten have a striking set of morphogenetic defects, including the failure to correctly specify the anterior-posterior body axis, that are not caused by changes in proliferation or cell death. The majority of Pten null embryos express markers of the primitive streak at ectopic locations around the embryonic circumference, rather than at a single site at the posterior of the embryo. Epiblast-specific deletion shows that Pten is not required in the cells of the primitive streak; instead, Pten is required for normal migration of cells of the Anterior Visceral Endoderm (AVE), an extraembryonic organizer that controls the po
SUBMITTER: Bloomekatz J
PROVIDER: S-EPMC3299915 | biostudies-literature | 2012 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA