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Identification and dissection of an enhancer controlling epithelial gene expression in skin

机译:识别和解剖增强控制 皮肤上皮基因表达

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摘要

Keratins 14 and 5 are the structural hallmarks of the basal keratinocytes of the epidermis and outer root sheath (ORS) of the hair follicle. Their genes are controlled in a tissue-specific manner and thus serve as useful tools to elucidate the regulatory mechanisms involved in keratinocyte-specific transcription. Previously we identified several keratinocyte-specific DNase I hypersensitive sites (HSs) in the 5′ regulatory sequences of the K14 gene and showed that a 700-bp regulatory domain encompassing HSs II and III can confer epidermal and ORS-specific gene expression in transgenic mice in vivo. Although HS II harbored much of the transactivation activity in vitro, it was not sufficient to restrict expression to keratinocytes in vivo. We now explore the HS III regulatory element. Surprisingly, this element on its own confers gene expression to the keratinocytes of the inner root sheath (IRS) of the hair follicle, whereas a 275-bp DNA fragment containing both HSs II and III shifts the expression from the IRS to the basal keratinocytes and ORS in vivo. Electrophoretic mobility-shift assays and mutational studies of HSs III reveal a role for CACCC-box binding proteins, Sp1 family members, and other factors adding to the list of previously described factors that are involved in keratinocyte-specific gene expression. These studies highlight a cooperative interaction of the two HSs domains and strengthen the importance of combinatorial play of transcription factors that govern keratinocyte-specific gene regulation.
机译:角蛋白14和5是表皮的基底角质形成细胞和毛囊的外根鞘(ORS)的结构特征。它们的基因以组织特异性方式控制,因此可作为阐明参与角质形成细胞特异性转录的调控机制的有用工具。以前,我们在K14基因的5'调控序列中发现了几个角质形成细胞特异的DNase I超敏位点(HSs),并显示了包含HSs II和III的700 bp调控域可在转基因小鼠中赋予表皮和ORS特异性基因表达体内。尽管HS II在体外具有许多反式激活活性,但在体内将表达限制在角质形成细胞中还是不够的。现在,我们探讨HS III的监管要素。出乎意料的是,该元素本身赋予毛囊内根鞘(IRS)的角质形成细胞基因表达,而同时包含HSs II和III的275-bp DNA片段将其表达从IRS转移至基底角质形成细胞和体内ORS。 HSs III的电泳迁移率变动分析和突变研究揭示了CACCC-box结合蛋白,Sp1家族成员和其他因素的作用,这些因素增加了先前描述的与角质形成细胞特异性基因表达有关的因素。这些研究突出了两个HS域之间的协同相互作用,并加强了控制角质形成细胞特异性基因调控的转录因子组合作用的重要性。

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