| First Author | Peng H | Year | 2017 |
| Journal | Reproduction | Volume | 154 |
| Issue | 3 | Pages | 145-151 |
| PubMed ID | 28630100 | Mgi Jnum | J:244909 |
| Mgi Id | MGI:5913688 | Doi | 10.1530/REP-16-0629 |
| Citation | Peng H, et al. (2017) NLRP2 and FAF1 deficiency blocks early embryogenesis in the mouse. Reproduction 154(3):145-151 |
| abstractText | Nlrp2 is a maternal effect gene specifically expressed by mouse ovaries; deletion of this gene from zygotes is known to result in early embryonic arrest. In the present study, we identified FAF1 protein as a specific binding partner of the NLRP2 protein in both mouse oocytes and preimplantation embryos. In addition to early embryos, both Faf1 mRNA and protein were detected in multiple tissues. NLRP2 and FAF1 proteins were co-localized to both the cytoplasm and nucleus during the development of oocytes and preimplantation embryos. Co-immunoprecipitation assays were used to confirm the specific interaction between NLRP2 and FAF1 proteins. Knockdown of the Nlrp2 or Faf1 gene in zygotes interfered with the formation of a NLRP2-FAF1 complex and led to developmental arrest during early embryogenesis. We therefore conclude that NLRP2 interacts with FAF1 under normal physiological conditions and that this interaction is probably essential for the successful development of cleavage-stage mouse embryos. Our data therefore indicated a potential role for NLRP2 in regulating early embryo development in the mouse. |
