| First Author | Kano S | Year | 2022 |
| Journal | Biochem Biophys Res Commun | Volume | 598 |
| Pages | 74-80 | PubMed ID | 35151207 |
| Mgi Jnum | J:321816 | Mgi Id | MGI:6890170 |
| Doi | 10.1016/j.bbrc.2022.01.127 | Citation | Kano S, et al. (2022) The role of the histone methyltransferase SET domain bifurcated 1 during palatal development. Biochem Biophys Res Commun 598:74-80 |
| abstractText | The histone methyltransferase SET domain bifurcated 1 (SETDB1) catalyzes the trimethylation of lysine 9 of histone H3, thereby regulating gene expression. In this study, we used conditional knockout mice, where Setdb1 was deleted only in neural crest cells (Setdb1(fl/fl,)(Wnt1-Cre +) mice), to clarify the role of SETDB1 in palatal development. Setdb1(fl/fl,)(Wnt1-Cre +) mice died shortly after birth due to a cleft palate with full penetration. Reduced palatal mesenchyme proliferation was seen in Setdb1(fl/fl,)(Wnt1-Cre +) mice, which might be a possible mechanism of cleft palate development. Quantitative RT-PCR and in situ hybridization showed that expression of the Pax9, Bmp4, Bmpr1a, Wnt5a, and Fgf10 genes, known to be important for palatal development, were markedly decreased in the palatal mesenchyme of Setdb1(fl/fl,)(Wnt1-Cre +) mice. Along with these phenomena, SMAD1/5/9 phosphorylation was decreased by the loss of Setdb1. Our results demonstrated that SETDB1 is indispensable for palatal development partially through its proliferative effect. Taken together with previous reports that PAX9 regulates BMP signaling during palatal development which implies that loss of Setdb1 may be involved in the cleft palate development by decreasing SMAD-dependent BMP signaling through Pax9. |
