| First Author | Marino S | Year | 2007 |
| Journal | PLoS One | Volume | 2 |
| Issue | 6 | Pages | e519 |
| PubMed ID | 17565372 | Mgi Jnum | J:126871 |
| Mgi Id | MGI:3762244 | Doi | 10.1371/journal.pone.0000519 |
| Citation | Marino S, et al. (2007) Mutants in the mouse NuRD/Mi2 component P66alpha are embryonic lethal. PLoS One 2(6):e519 |
| abstractText | BACKGROUND: The NuRD/Mi2 chromatin complex is involved in histone modifications and contains a large number of subunits, including the p66 protein. There are two mouse and human p66 paralogs, p66alpha and p66beta. The functions of these genes are not clear, in part because there are no mutants available, except in invertebrate model systems. METHODOLOGY: We made loss of function mutants in the mouse p66alpha gene (mp66alpha, official name Gatad2a, MGI:2384585). We found that mp66alpha is essential for development, as mutant embryos die around day 10 of embryogenesis. The gene is not required for normal blastocyst development or for implantation. The phenotype of mutant embryos and the pattern of gene expression in mutants are consistent with a role of mp66alpha in gene silencing. CONCLUSION: mp66alpha is an essential gene, required for early mouse development. The lethal phenotype supports a role in execution of methylated DNA silencing. |
