Abstract
Previous studies have shown that Oct4 has an essential role in maintaining pluripotency of cells of the inner cell mass (ICM) and embryonic stem cells. However, Oct4 null homozygous embryos die around the time of implantation, thus precluding further analysis of gene function during development. We have used the conditional Cre/loxP gene targeting strategy to assess Oct4 function in primordial germ cells (PGCs). Loss of Oct4 function leads to apoptosis of PGCs rather than to differentiation into a trophectodermal lineage, as has been described for Oct4-deficient ICM cells. These new results suggest a previously unknown function of Oct4 in maintaining viability of mammalian germline.
MeSH Terms
Alleles
Animals
Apoptosis
Cell Differentiation
Cell Lineage
Cell Survival
DNA-Binding Proteins/physiology
Embryo, Mammalian/cytology
Extracellular Matrix/metabolism
Female
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genetic Vectors
Germ Cells/cytology
Homozygote
In Situ Nick-End Labeling
Male
Mice
Mice, Transgenic
Models, Genetic
Octamer Transcription Factor-3
Phenotype
Signal Transduction
Stem Cells/cytology
Time Factors
Transcription Factors/physiology
Chemicals
DNA-Binding Proteins
Octamer Transcription Factor-3
Pou5f1 protein, mouse
Transcription Factors
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Kehler James
Germline Development, Center for Animal Transgenesis and Germ Cell Research, New Bolton Center, University of Pennsylvania, 382 W. Street Road, Kennett Square, Pennsylvania 19348, USA.
Tolkunova Elena
Koschorz Birgit
Pesce Maurizio
Gentile Luca
Boiani Michele
Lomelí Hilda
Nagy Andras
McLaughlin K John
Schöler Hans R
Tomilin Alexey
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