| First Author | Hashimoto M | Year | 2015 |
| Journal | Dev Growth Differ | Volume | 57 |
| Issue | 7 | Pages | 529-38 |
| PubMed ID | 26178919 | Mgi Jnum | J:223645 |
| Mgi Id | MGI:5659939 | Doi | 10.1111/dgd.12232 |
| Citation | Hashimoto M, et al. (2015) Nepro is localized in the nucleolus and essential for preimplantation development in mice. Dev Growth Differ 57(7):529-38 |
| abstractText | We generated knockout (KO) mice of Nepro, which has been shown to be necessary to maintain neural progenitor cells downstream of Notch in the mouse developing neocortex by using knockdown experiments, to explore its function in embryogenesis. Nepro KO embryos were morphologically indistinguishable from wild type (WT) embryos until the morula stage but failed in blastocyst formation, and many cells of the KO embryos resulted in apoptosis. We found that Nepro was localized in the nucleolus at the blastocyst stage. The number of nucleolus precursor bodies (NPBs) and nucleoli per nucleus was significantly higher in Nepro KO embryos compared with WT embryos later than the 2-cell stage. Furthermore, at the morula stage, whereas 18S rRNA and ribosomal protein S6 (rpS6), which are components of the ribosome, were distributed to the cytoplasm in WT embryos, they were mainly localized in the nucleoli in Nepro KO embryos. In addition, in Nepro KO embryos, the amount of the mitochondria-associated p53 protein increased, and Cytochrome c was distributed in the cytoplasm. These findings indicate that Nepro is a nucleolus-associated protein, and its loss leads to the apoptosis before blastocyst formation in mice. |
