Osada Motonobu, Park Hannah Lui, Nagakawa Yuichi, Yamashita Keishi, Fomenkov Alexey, Kim Myoung Sook, Wu Guojun, Nomoto Shuji, Trink Barry, Sidransky David
Department of Otolaryngology, Division of Head and Neck Surgery, Johns Hopkins University School of Medicine, 818 Ross Research Building, 720 Rutland Avenue, Baltimore, Maryland 21205, USA.
Mol Cell Biol. 2005 Jul;25(14):6077-89. doi: 10.1128/MCB.25.14.6077-6089.2005.
p63 is a member of the p53 tumor suppressor gene family, which regulates downstream target gene expression by binding to sequence-specific response elements similar to those of p53. By using oligonucleotide expression microarray analysis and analyzing the promoters of p63-induced genes, we have identified novel p63-specific response elements (p63-REs) in the promoter regions of EVPL and SMARCD3. These p63-REs exhibit characteristic differences from the canonical p53-RE (RRRCWWGYYY) in both the core-binding element (CWWG) as well as the RRR and/or YYY stretches. Luciferase assays on mutagenized promoter constructs followed by electromobility shift analysis showed that p53 preferentially activates and binds to the RRRCATGYYY sequence, whereas p63 preferentially activates RRRCGTGYYY. Whereas EVPL protein is highly expressed in epithelial cells of the skin and pharynx in the p63+/+ mouse, it is undetectable in these tissues in the p63-/- mouse. Our results indicate that p63 can regulate expression of specific target genes such as those involved in skin, limb, and craniofacial development by preferentially activating distinct p63-specific response elements.
p63是p53肿瘤抑制基因家族的成员,它通过与类似于p53的序列特异性反应元件结合来调节下游靶基因的表达。通过使用寡核苷酸表达微阵列分析并分析p63诱导基因的启动子,我们在EVPL和SMARCD3的启动子区域中鉴定出了新的p63特异性反应元件(p63-REs)。这些p63-REs在核心结合元件(CWWG)以及RRR和/或YYY序列上与典型的p53-RE(RRRCWWGYYY)表现出特征性差异。对诱变的启动子构建体进行荧光素酶测定,随后进行电泳迁移率变动分析,结果表明p53优先激活并结合RRRCATGYYY序列,而p63优先激活RRRCGTGYYY。在p63+/+小鼠中,EVPL蛋白在皮肤和咽部的上皮细胞中高度表达,而在p63-/-小鼠的这些组织中则检测不到。我们的结果表明,p63可以通过优先激活不同的p63特异性反应元件来调节特定靶基因的表达,例如那些参与皮肤、肢体和颅面发育的基因。