Shiohara M, Shigemura T, Suzuki T, Tanaka M, Morii E, Ohtsu H, Shibahara S, Koike K
Department of Pediatrics, Shinshu University School of Medicine, Asahi, Matsumoto, Japan.
Int J Lab Hematol. 2009 Apr;31(2):215-26. doi: 10.1111/j.1751-553X.2008.01028.x. Epub 2008 Feb 16.
The microphthalmia-associated transcription factor (MITF) gene encodes a basic helix-loop-helix and leucin zipper protein. In this study, we identified a novel MITF isoform, MITF-CM, which possesses a unique amino terminus. Exon 1CM is located 84 kb upstream of the exon encoding the B1b domain. MITF-CM was expressed in the human mast cell line HMC-1, the human basophilic cell line KU812, and CB-derived mast cells cultured for 10 weeks as well as bone marrow mononuclear cells. Transient transfection of MITF-CM cDNA in COS-7 cells resulted in the expression of a 64-kDa protein, detected by Western blotting, and nuclear localization of the protein, detected by immunostaining. The transient cotransfection of a luciferase construct under the control of the tyrosinase promoter and MITF-CM cDNA increased luciferase activity threefold. In contrast, none of the MITF isoforms transactivated both the tryptase and chymase gene promoters, indicating differences in the gene transactivation system between humans and mice.
小眼畸形相关转录因子(MITF)基因编码一种碱性螺旋-环-螺旋和亮氨酸拉链蛋白。在本研究中,我们鉴定出一种新型的MITF异构体,即MITF-CM,它具有独特的氨基末端。外显子1CM位于编码B1b结构域的外显子上游84 kb处。MITF-CM在人肥大细胞系HMC-1、人嗜碱性细胞系KU812、培养10周的CB来源肥大细胞以及骨髓单个核细胞中表达。将MITF-CM cDNA瞬时转染到COS-7细胞中,通过蛋白质印迹法检测到表达了一种64 kDa的蛋白质,通过免疫染色检测到该蛋白质的核定位。在酪氨酸酶启动子控制下的荧光素酶构建体与MITF-CM cDNA的瞬时共转染使荧光素酶活性增加了三倍。相比之下,没有一种MITF异构体能激活类胰蛋白酶和糜蛋白酶基因启动子,这表明人与小鼠之间的基因反式激活系统存在差异。