Kaufman Charles K, Sinha Satrajit, Bolotin Diana, Fan Jie, Fuchs Elaine
Department of Molecular Genetics and Cell Biology, Howard Hughes Medical Institute, The University of Chicago, Chicago, Illinois 60637, USA.
Mol Cell Biol. 2002 Jun;22(12):4293-308. doi: 10.1128/MCB.22.12.4293-4308.2002.
In this report, we explored the mechanisms underlying keratinocyte-specific and differentiation-specific gene expression in the skin. We have identified five keratinocyte-specific, open chromatin regions that exist within the 6 kb of 5' upstream regulatory sequence known to faithfully recapitulate the strong endogenous keratin 5 (K5) promoter and/or enhancer activity. One of these, DNase I-hypersensitive site (HSs) 4, was unique in that it acted independently to drive abundant and keratinocyte-specific reporter gene activity in culture and in transgenic mice, despite the fact that it was not essential for K5 enhancer activity. We have identified evolutionarily conserved regulatory elements and a number of their associated proteins that bind to this compact and complex enhancer element. The 125-bp 3' half of this element (referred to as 4.2) is by far the smallest known strong enhancer element possessing keratinocyte-specific activity in vivo. Interestingly, its activity is restricted to a subset of progeny of K5-expressing cells located within the sebaceous gland. The other half of HSs 4 (termed 4.1) possesses activity to suppress sebocyte-specific expression and induce expression in the channel (inner root sheath) cells surrounding the hair shaft. Our findings lead us to a view of keratinocyte gene expression which is determined by multiple regulatory modules, many of which contain AP-2 and/or Sp1/Sp3 binding sites for enhancing expression in skin epithelium, but which also harbor one or more unique sites for the binding of factors which determine specificity. Through mixing and matching of these modules, additional levels of specificity are obtained, indicating that both transcriptional repressors and activators govern the specificity.
在本报告中,我们探究了皮肤中角质形成细胞特异性和分化特异性基因表达的潜在机制。我们鉴定出五个角质形成细胞特异性的开放染色质区域,它们存在于已知能忠实地重现内源性角蛋白5(K5)强启动子和/或增强子活性的5'上游调控序列的6 kb范围内。其中之一,即DNA酶I超敏位点(HSs)4,其独特之处在于,尽管它对K5增强子活性并非必需,但它在培养细胞和转基因小鼠中能独立驱动丰富的角质形成细胞特异性报告基因活性。我们鉴定出了进化上保守的调控元件以及许多与之结合的相关蛋白,这些蛋白与这个紧凑而复杂的增强子元件相结合。该元件3'端的125 bp片段(称为4.2)是目前已知在体内具有角质形成细胞特异性活性的最小的强增强子元件。有趣的是,其活性仅限于皮脂腺内表达K5的细胞的子代中的一个子集。HSs 4的另一半(称为4.1)具有抑制皮脂腺细胞特异性表达并诱导毛干周围通道(内根鞘)细胞表达的活性。我们的研究结果使我们对角质形成细胞基因表达形成了一种观点,即它由多个调控模块决定,其中许多模块含有AP - 2和/或Sp1/Sp3结合位点以增强在皮肤上皮中的表达,但也含有一个或多个决定特异性的因子结合的独特位点。通过这些模块的混合和匹配,可获得额外的特异性水平,这表明转录抑制因子和激活因子都控制着特异性。