Lersch R, Stellmach V, Stocks C, Giudice G, Fuchs E
Department of Molecular Genetics and Cell Biology, Howard Hughes Medical Institute, University of Chicago, Illinois 60637.
Mol Cell Biol. 1989 Sep;9(9):3685-97. doi: 10.1128/mcb.9.9.3685-3697.1989.
The mitotically active basal layers of most stratified squamous epithelia express 10 to 30% of their total protein as keratin. The two keratins specifically expressed in these cells are the type II keratin K5 (58 kilodaltons) and its corresponding partner, type I keratin K14 (50 kilodaltons), both of which are essential for the formation of 8-nm filaments. Dissecting the molecular mechanisms underlying the coordinate regulation of the two keratins is an important first step in understanding epidermal differentiation and in designing promoters that will enable delivery and expression of foreign gene products in stratified squamous epithelia, e.g., skin. Previously, we reported the sequence of the gene encoding human K14 (D. Marchuk, S. McCrohon, and E. Fuchs, Cell 39:491-498, 1984; Marchuk et al., Proc. Natl. Acad. Sci. USA 82:1609-1613, 1985). We have now isolated and characterized the gene encoding human K5. The sequence of the coding portion of this gene matched perfectly with that of a partial K5 cDNA sequence obtained from a cultured human epidermal library (R. Lersch and E. Fuchs, Mol. Cell. Biol. 8:486-493, 1988), and gene transfection studies indicated that the gene is functional. Nuclear runoff experiments demonstrated that the K5 and K14 genes were both transcribed at dramatically higher levels in cultured human epidermal cells than in fibroblasts, indicating that at least part of the regulation of the expression of this keratin pair is at the transcriptional level. When the K5 gene was transfected transiently into NIH 3T3 fibroblasts, foreign expression of the gene caused the appearance of endogenous mouse K14 and the subsequent formation of a keratin filament array in the cells. In this case, transcriptional changes did not appear to be involved in the regulation, suggesting that there may be multiple control mechanisms underlying the pairwise expression of keratins.
大多数复层鳞状上皮的有丝分裂活跃的基底层表达的角蛋白占其总蛋白的10%至30%。在这些细胞中特异性表达的两种角蛋白是II型角蛋白K5(58千道尔顿)及其相应的伙伴I型角蛋白K14(50千道尔顿),二者对于8纳米细丝的形成均至关重要。剖析这两种角蛋白协同调控的分子机制,是理解表皮分化以及设计能够使外源基因产物在复层鳞状上皮(如皮肤)中递送和表达的启动子的重要第一步。此前,我们报道了编码人K14的基因序列(D. 马尔丘克、S. 麦克罗洪和E. 富克斯,《细胞》39:491 - 498,1984年;马尔丘克等人,《美国国家科学院院刊》82:1609 - 1613,1985年)。我们现在已经分离并鉴定了编码人K5的基因。该基因编码部分的序列与从培养的人表皮文库中获得的部分K5 cDNA序列完全匹配(R. 勒施和E. 富克斯,《分子与细胞生物学》8:486 - 493,1988年),并且基因转染研究表明该基因具有功能。核转录实验表明,K5和K14基因在培养的人表皮细胞中的转录水平均显著高于成纤维细胞,这表明这对角蛋白表达调控的至少部分作用发生在转录水平。当将K5基因瞬时转染到NIH 3T3成纤维细胞中时,该基因的外源表达导致内源性小鼠K14出现,并随后在细胞中形成角蛋白丝阵列。在这种情况下,转录变化似乎不参与调控,这表明角蛋白成对表达可能存在多种控制机制。