Perez Carmen A, Pietenpol Jennifer A
Department of Biochemistry, Center in Molecular Toxicology, The Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Cell Cycle. 2007 Feb 1;6(3):246-54. doi: 10.4161/cc.6.3.3801. Epub 2007 Feb 3.
The transcription factor p63 belongs to a family of regulatory proteins that bind DNA in a sequence-specific manner, close to a target gene, to activate or repress its transcription. These proteins display a striking conservation of functional domains, but are differentially involved in regulating cellular processes. Nearly a decade after the discovery of p63, its critical role for proper epithelial development, maintenance and tumorigenesis is widely recognized. Several important cellular endpoints have been linked to p63 regulation in epithelium, including differentiation, cell fate specification, proliferation, survival, senescence, apoptosis, cell-cell and cell-matrix interaction programs. Although a large number of genes have been associated with p63-dependent regulation, only a few of these have been validated as direct p63 transcriptional targets. The challenge still remains to define the p63 transcriptome in epithelial cells, and to dissect the cellular mechanisms used to modulate the expression of this transcriptional profile. In this article we will review current knowledge regarding the basic mechanisms used by p63 to regulate gene expression. Also, we will discuss specific p63-regulated biological endpoints in epithelial cells and the specific genes that have been linked to p63 regulation in these particular contexts.
转录因子p63属于一类调控蛋白家族,这类蛋白以序列特异性方式结合于靶基因附近的DNA,以激活或抑制其转录。这些蛋白在功能结构域上表现出显著的保守性,但在调节细胞过程中发挥着不同的作用。在p63被发现近十年后,其在正常上皮发育、维持和肿瘤发生中的关键作用已得到广泛认可。上皮细胞中的几个重要细胞终点已与p63调控相关联,包括分化、细胞命运决定、增殖、存活、衰老、凋亡、细胞间和细胞与基质相互作用程序。尽管大量基因已与p63依赖性调控相关,但其中只有少数已被验证为直接的p63转录靶标。确定上皮细胞中的p63转录组,并剖析用于调节这种转录谱表达的细胞机制,仍然是一项挑战。在本文中,我们将综述关于p63用于调控基因表达的基本机制的当前知识。此外,我们将讨论上皮细胞中特定的p63调控的生物学终点,以及在这些特定情况下与p63调控相关的特定基因。