Ueda E, Ohno S, Kuroki T, Livneh E, Yamada K, Yamanishi K, Yasuno H
Department of Dermatology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
J Biol Chem. 1996 Apr 19;271(16):9790-4. doi: 10.1074/jbc.271.16.9790.
Transglutaminase 1 (TGase 1) is expressed during the terminal differentiation of keratinized squamous epithelium to form cornified cell envelope in differentiated keratinocytes by the epsilon-(gamma-glutamyl) cross-linking reaction. The gene for human TGase 1 is responsible for autosomal recessive lamellar ichthyosis, a severe hereditary keratinizing disorder of the skin. We examined the transcriptional activity of the gene in FRSK, rat keratinocytic cells, transfected with the luciferase reporter gene under control of the 5' upstream region of human TGase 1 gene. Transfection of the reporter gene with an expression vector for the eta isoform of novel protein kinase C (nPKCeta), as well as exposure to 12-0-tetradecanoylphorbol-13-acetate, markedly increased the luciferase activity in FRSK, but not in HT-1080 fibrosarcoma cells, although exogenous nPKCeta was expressed in both. The induction was suppressed by deleting the TGase 1 upstream sequence from -95 to -67 and by deleting the kinase domain from exogenous nPKCeta. In comparison with other PKC isoforms, nPKCeta most effectively induced the luciferase activity. We suggest that nPKCeta, an epithelium-specific isoform of PKC, mediates the activation of the TGase 1 transcription.
转谷氨酰胺酶1(TGase 1)在角质化鳞状上皮的终末分化过程中表达,通过ε-(γ-谷氨酰)交联反应在分化的角质形成细胞中形成角化细胞包膜。人类TGase 1基因与常染色体隐性板层状鱼鳞病相关,这是一种严重的遗传性皮肤角化障碍。我们检测了在人TGase 1基因5'上游区域控制下,用荧光素酶报告基因转染的大鼠角质形成细胞FRSK中该基因的转录活性。用新型蛋白激酶C(nPKCeta)的η亚型表达载体转染报告基因,以及用12-0-十四烷酰佛波醇-13-乙酸酯处理,均显著增加了FRSK中的荧光素酶活性,但在HT-1080纤维肉瘤细胞中未增加,尽管两种细胞中外源nPKCeta均有表达。通过删除TGase 1上游序列-95至-67以及从外源nPKCeta中删除激酶结构域,诱导作用受到抑制。与其他PKC亚型相比,nPKCeta最有效地诱导了荧光素酶活性。我们认为,PKC的上皮特异性亚型nPKCeta介导了TGase 1转录的激活。