Fontemaggi Giulia, Gurtner Aymone, Damalas Alexander, Costanzo Antonio, Higashi Yujiro, Sacchi Ada, Strano Sabrina, Piaggio Giulia, Blandino Giovanni
Department of Experimental Oncology, Regina Elena Cancer Institute, 00158 Rome, Italy.
Oncogene. 2005 Nov 10;24(49):7273-80. doi: 10.1038/sj.onc.1208891.
The discovery of two new p53 homologs, p73 and p63, has defined a family of transcription factors heavily involved in the control of growth suppression, apoptosis, differentiation and development. While p53-deficient mice undergo spontaneous tumors, p73 and p63 knockout mice exhibit severe developmental defects. We demonstrate here that p73 gene is an in vivo transcriptional target of the muscle regulatory factors MyoD, myogenin, Myf5 and Myf6. Ectopic expression of the transcriptional repressor deltaEF1/ZEB/zfhx1a counteracts MyoD/Myf5- or MyoD/Myf6-mediated transcriptional activation of p73. A distinct pattern of in vivo recruitment of muscle regulatory factors and deltaEF1 on p73 regulatory regions was found between proliferating and differentiating muscle cells. We also found that deltaEF1 plays a role in the transcriptional regulation of p53 family members during keratinocytic differentiation. Mouse embryo fibroblasts derived from deltaEF1-deficient mice exhibit unbalanced expression of DeltaNp63, TAp73 and DeltaNp73 but not of TAp63 and p53. The analysis of tissues derived from deltaEF1+/- mice exhibit a selective enrichment of DeltaNp63 in skin.
两种新的p53同源物p73和p63的发现,界定了一个转录因子家族,该家族在生长抑制、细胞凋亡、分化及发育的调控过程中发挥着重要作用。p53基因缺陷的小鼠会自发形成肿瘤,而p73和p63基因敲除的小鼠则表现出严重的发育缺陷。我们在此证明,p73基因是肌肉调节因子MyoD、肌细胞生成素、Myf5和Myf6在体内的转录靶点。转录抑制因子deltaEF1/ZEB/zfhx1a的异位表达可抵消MyoD/Myf5或MyoD/Myf6介导的p73转录激活。在增殖和分化的肌肉细胞之间,发现了肌肉调节因子和deltaEF1在p73调控区域的体内募集模式存在差异。我们还发现,deltaEF1在角质形成细胞分化过程中对p53家族成员的转录调控发挥作用。源自deltaEF1基因缺陷小鼠的小鼠胚胎成纤维细胞表现出DeltaNp63、TAp73和DeltaNp73表达失衡,但TAp63和p53无此现象。对源自deltaEF1+/-小鼠的组织分析显示,DeltaNp63在皮肤中选择性富集。