Sinha S, Fuchs E
Howard Hughes Medical Institute, Department of Molecular Genetics and Cell Biology, University of Chicago, 5841 South Maryland Avenue, Chicago, IL 60637, USA.
Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2455-60. doi: 10.1073/pnas.051633598.
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.
角蛋白14和5是表皮基底角质形成细胞以及毛囊外根鞘(ORS)的结构标志。它们的基因以组织特异性方式受到调控,因此是阐明角质形成细胞特异性转录所涉及调控机制的有用工具。此前我们在K14基因的5'调控序列中鉴定出了几个角质形成细胞特异性的脱氧核糖核酸酶I超敏位点(HSs),并表明一个包含HSs II和III的700碱基对调控结构域能够在体内转基因小鼠中赋予表皮和ORS特异性基因表达。尽管HS II在体外具有大部分反式激活活性,但它并不足以在体内将表达限制在角质形成细胞中。我们现在探究HS III调控元件。令人惊讶的是,该元件自身就能赋予毛囊内根鞘(IRS)角质形成细胞基因表达,而一个同时包含HSs II和III的275碱基对DNA片段在体内会使表达从IRS转移至基底角质形成细胞和ORS。HSs III的电泳迁移率变动分析和突变研究揭示了CACCC框结合蛋白、Sp1家族成员以及其他因子的作用,这些因子加入了先前描述的参与角质形成细胞特异性基因表达的因子列表中。这些研究突出了两个HS结构域的协同相互作用,并强化了转录因子组合作用在调控角质形成细胞特异性基因表达中的重要性。