Asano H, Ishida A, Hasegawa M, Ono T, Yoshida M C, Taniguchi M, Kanno M
Division of Molecular Immunology, School of Medicine, Chiba University, Japan.
DNA Seq. 1993;3(6):369-77. doi: 10.3109/10425179309020838.
The chromosome gene for mouse Mel-18 (mMel-18) protein has been isolated and characterized. The entire mMel-18 gene is composed of thirteen exons spanning about 15 kilobases, in which the protein is encoded by exons 5-13. The "RING-finger" motif of Mel-18 protein that displays a significant evolutionary resemblance to other RING-finger nuclear proteins is encoded by exons 5 and 6. Exon 13 encodes a C-terminal proline/serine-rich domain that is homologous to some transactivator proteins. Sequence analysis of the 5'-flanking region revealed the presence of potential binding sites for transcription factors such as SP-1, NF-1, NF-kappa B and c-myc/max. At least two major cap sites and three minor cap sites were identified by S1 mapping and primer extension analysis. We propose that the mMel-18 gene is regulated by two different types of promoters, the CAAT-TATA box promoter and the GC-rich TATA-less promoter. The 2.4 kb DNA fragment of the 5'-flanking region exhibited constitutive promoter activity when transfected into L cells. By the in situ hybridization method, the mMel-18 gene was assigned to mouse chromosome 10C3.
小鼠Mel-18(mMel-18)蛋白的染色体基因已被分离和鉴定。整个mMel-18基因由13个外显子组成,跨度约15千碱基,其中蛋白质由外显子5 - 13编码。Mel-18蛋白的“环指”基序与其他环指核蛋白有显著的进化相似性,由外显子5和6编码。外显子13编码一个与一些反式激活蛋白同源的C末端富含脯氨酸/丝氨酸的结构域。对5'侧翼区域的序列分析揭示了存在转录因子如SP-1、NF-1、NF-κB和c-myc/max的潜在结合位点。通过S1作图和引物延伸分析鉴定出至少两个主要的帽位点和三个次要的帽位点。我们提出mMel-18基因受两种不同类型的启动子调控,即CAAT-TATA盒启动子和富含GC的无TATA启动子。当将5'侧翼区域的2.4 kb DNA片段转染到L细胞中时,它表现出组成型启动子活性。通过原位杂交方法,mMel-18基因被定位到小鼠染色体10C3。