Journal article

Heterozygous expression of the oncogenic Pik3caH1047R mutation during murine development results in fatal embryonic and extraembryonic defects

LM Hare, Q Schwarz, S Wiszniak, R Gurung, KG Montgomery, CA Mitchell, WA Phillips

Developmental Biology | ACADEMIC PRESS INC ELSEVIER SCIENCE | Published : 2015

Abstract

The phosphoinositide 3-kinase (PI3K)/AKT signalling pathway regulates many cellular functions including proliferation, migration, survival and protein synthesis. Somatic mutations in PIK3CA, the gene encoding the p110α catalytic subunit of PI3K enzyme, are commonly associated with many human cancers as well as recently being implicated in human overgrowth syndromes. However, it is not clear if such mutations can be inherited through the germline. We have used a novel mouse model with Cre recombinase (Cre)-conditional knock-in of the common H1047R mutation into the endogenous Pik3ca gene. Heterozygous expression of the Pik3caH1047R mutation in the developing mouse embryo resulted in failed 't..

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University of Melbourne Researchers