Kawakami K, Ohto H, Ikeda K, Roeder R G
Department of Biology, Jichi Medical School, Tochigi, Japan.
Nucleic Acids Res. 1996 Jan 15;24(2):303-10. doi: 10.1093/nar/24.2.303.
The cDNA clones encoding ARE(Na,K-ATPase alpha1 subunit gene regulatory element) binding protein AREC3 were isolated from myoblast C2C12 cells and mouse skeletal muscle cDNA library. At least four alternatively spliced forms of AREC3 cDNA were identified. Sequence analysis indicates that AREC3 has an extensive homology with the Drosophila sine oculis gene product required for development of the entire visual system [Cheyette et al.(1994) Neuron 12, 977-996]. The homologous region including a homeodomain is required for specific DNA binding to ARE. A transactivation domain was identified in the C-terminal part of the AREC3 by reporter gene assays using GAL4-AREC3 fusion protein constructs. Immunohistochemistry revealed that AREC3 localized to the nucleus and cytoplasm of myoblast C2C12 cells, and the production of AREC3 is augmented during muscle differentiation. Western blot analysis indicated that the 115 kDa form of AREC3 protein is increased in the cytoplasmic extract, and the 67kDa form is increased both in nuclear and cytoplasmic extracts of C2C12 cells during muscle differentiation.
从成肌细胞C2C12细胞和小鼠骨骼肌cDNA文库中分离出编码ARE(钠钾ATP酶α1亚基基因调控元件)结合蛋白AREC3的cDNA克隆。鉴定出至少四种AREC3 cDNA的可变剪接形式。序列分析表明,AREC3与整个视觉系统发育所需的果蝇无眼基因产物具有广泛的同源性[Cheyette等人(1994年)《神经元》12卷,977 - 996页]。与ARE特异性DNA结合所需的同源区域包括一个同源异型结构域。通过使用GAL4 - AREC3融合蛋白构建体的报告基因分析,在AREC3的C末端部分鉴定出一个反式激活结构域。免疫组织化学显示,AREC3定位于成肌细胞C2C12细胞的细胞核和细胞质中,并且在肌肉分化过程中AREC3的产生增加。蛋白质免疫印迹分析表明,在肌肉分化过程中,C2C12细胞细胞质提取物中115 kDa形式的AREC3蛋白增加,而细胞核和细胞质提取物中67 kDa形式的AREC3蛋白均增加。