De Rosa Laura, Antonini Dario, Ferone Giustina, Russo Monia T, Yu Paul B, Han Rong, Missero Caterina
CEINGE Biotecnologie Avanzate, via Comunale Margherita 482, 80145 Napoli, Italy.
J Biol Chem. 2009 Oct 30;284(44):30574-82. doi: 10.1074/jbc.M109.049619. Epub 2009 Aug 28.
p63, a p53 family member, plays an essential role in epidermal development by regulating its transcriptional program. Here we report a previously uncovered role of p63 in controlling bone morphogenetic protein (BMP) signaling, which is required for maintaining low expression levels of several non-epidermal genes. p63 represses transcription of the inhibitory Smad7 and activates Bmp7, thereby sustaining BMP signaling. In the absence of p63, compromised BMP signaling leads to inappropriate non-epidermal gene expression in postnatal mouse keratinocytes and in embryonic epidermis. Reactivation of BMP signaling by Smad7 knockdown and/or, to a lesser extent, by BMP treatment suppresses expression of non-epidermal genes in the absence of p63. Canonical BMP/Smad signaling is essential for control of non-epidermal genes as use of a specific inhibitor, or simultaneous knockdown of Smad1 and Smad5 counteract suppression of non-epidermal genes. Our data indicate that p63 prevents ectopic expression of non-epidermal genes by a mechanism involving Smad7 repression and, to a lesser extent, Bmp7 induction, with consequent enhancement of BMP/Smad signaling.
p63是一种p53家族成员,通过调节其转录程序在表皮发育中发挥重要作用。在此,我们报告了p63在控制骨形态发生蛋白(BMP)信号传导方面一个先前未被发现的作用,该信号传导对于维持几个非表皮基因的低表达水平是必需的。p63抑制抑制性Smad7的转录并激活Bmp7,从而维持BMP信号传导。在缺乏p63的情况下,受损的BMP信号传导导致出生后小鼠角质形成细胞和胚胎表皮中出现不适当的非表皮基因表达。通过敲低Smad7和/或在较小程度上通过BMP处理来重新激活BMP信号传导,可在缺乏p63的情况下抑制非表皮基因的表达。经典的BMP/Smad信号传导对于控制非表皮基因至关重要,因为使用特异性抑制剂或同时敲低Smad1和Smad5会抵消对非表皮基因的抑制作用。我们的数据表明,p63通过一种涉及抑制Smad7以及在较小程度上诱导Bmp7的机制来防止非表皮基因的异位表达,从而增强BMP/Smad信号传导。