| First Author | Bösl MR | Year | 1997 |
| Journal | Proc Natl Acad Sci U S A | Volume | 94 |
| Issue | 11 | Pages | 5531-4 |
| PubMed ID | 9159106 | Mgi Jnum | J:40911 |
| Mgi Id | MGI:892630 | Doi | 10.1073/pnas.94.11.5531 |
| Citation | Bosl MR, et al. (1997) Early embryonic lethality caused by targeted disruption of the mouse selenocysteine tRNA gene (Trsp). Proc Natl Acad Sci U S A 94(11):5531-4 |
| abstractText | Selenoprotein biosynthesis is mediated by tRNA(Sec), which inserts selenocysteine at UGA codons in a complex, context- specific manner, This opal suppressor serves in the conversion of serine to selenocysteine as well, The mouse tRNA(Sec) gene (Trsp) maps to a proximal segment of chromosome 7. We constructed mice carrying a targeted deletion of the Trsp gene, The heterozygous mutants were viable, fertile, and appeared normal, Although the level of tRNA(Sec) was reduced to about 50%-80% of the wild type in most organs, one of the selenoproteins, glutathione peroxidase, remained unaffected in the levels of its mRNA, protein, and enzyme activity, indicating that the haploid amount of tRNA(Sec) is not limiting in its biosynthesis. In contrast, the homozygous mutants died shortly after implantation, and the embryos were resorbed before 6.5 days post coitum, When the preimplantation embryos were placed in culture, however, the trophoectoderm cells showed outgrowths and the inner cell mass cells of the homozygous embryos were able to proliferate. These results indicate that Trsp expression is essential for early development of the embryo, and its lack causes periimplantation lethality. However, the lethality does not appear to be due to a cell-autonomous function of tRNA(Sec). |
