Transforming growth factor β€ (TGF-β€) is a potent inhibitor of hepatocyte proliferation in vitro and is suggested to be a key negative regulator of liver growth. To directly address the role of TGF-β€ signaling in liver regeneration in vivo, the TGF-β€ type II receptor gene (Tgfbr2) was selectively del
Dppa3 / Pgc7 / stellais a maternal factor and is not required for germ cell specification in mice
β Scribed by Alex Bortvin; Mary Goodheart; Michelle Liao; David C Page
- Book ID
- 104492640
- Publisher
- BioMed Central
- Year
- 2004
- Tongue
- English
- Weight
- 652 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1471-213X
No coin nor oath required. For personal study only.
β¦ Synopsis
Background: In mice, germ cells are specified through signalling between layers of cells comprising the primitive embryo. The function of Dppa3 (also known as Pgc7 or stella), a gene expressed in primordial germ cells at the time of their emergence in gastrulating embryos, is unknown, but a recent study has claimed that it plays a central role in germ cell specification.
Results:
To test Dppa3's role in germ cell development, we disrupted the gene in mouse embryonic stem cells and generated mutant animals. We were able to obtain viable and fertile Dppa3-deficient animals of both sexes. Examination of embryonic and adult germ cells and gonads in Dppa3-deficient animals did not reveal any defects. However, most embryos derived from Dppa3-deficient oocytes failed to develop normally beyond the four-cell stage.
Conclusion:
We found that Dppa3 is an important maternal factor in the cleavage stages of mouse embryogenesis. However, it is not required for germ cell specification.
π SIMILAR VOLUMES