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A composite enhancer regulates p63 gene expression in epidermal morphogenesis and in keratinocyte differentiation by multiple mechanisms

机译:复合增强剂通过多种机制调节表皮形态发生和角质形成细胞分化中的p63基因表达。

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摘要

p63 is a crucial regulator of epidermal development, but its transcriptional control has remained elusive. Here, we report the identification of a long-range enhancer (p63LRE) that is composed of two evolutionary conserved modules (C38 and C40), acting in concert to control tissue- and layer-specific expression of the p63 gene. Both modules are in an open and active chromatin state in human and mouse keratinocytes and in embryonic epidermis, and are strongly bound by p63. p63LRE activity is dependent on p63 expression in embryonic skin, and also in the commitment of human induced pluripotent stem cells toward an epithelial cell fate. A search for other transcription factors involved in p63LRE regulation revealed that the CAAT enhancer binding proteins Cebpa and Cebpb and the POU domain-containing protein Pou3f1 repress p63 expression during keratinocyte differentiation by binding the p63LRE enhancer. Collectively, our data indicate that p63LRE is composed of additive and partly redundant enhancer modules that act to direct robust p63 expression selectively in the basal layer of the epidermis.
机译:p63是表皮发育的关键调节因子,但其转录控制仍然难以捉摸。在这里,我们报告鉴定由两个进化保守模块(C38和C40)组成的远程增强子(p63LRE),它们协同作用以控制p63基因的组织和层特异性表达。这两个模块在人和小鼠的角质形成细胞和胚胎表皮中均处于开放和活跃的染色质状态,并被p63强烈结合。 p63LRE活性取决于胚胎皮肤中p63的表达,还取决于人类诱导的多能干细胞对上皮细胞命运的参与。对参与p63LRE调控的其他转录因子的搜索显示,CAAT增强子结合蛋白Cebpa和Cebpb以及含POU域的蛋白Pou3f1通过与p63LRE增强子结合来抑制角质形成细胞分化过程中的p63表达。总体而言,我们的数据表明p63LRE由累加的和部分冗余的增强子模块组成,这些模块起着在表皮基底层中选择性引导稳健的p63表达的作用。

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