Carthew R W, Chodosh L A, Sharp P A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Genes Dev. 1987 Nov;1(9):973-80. doi: 10.1101/gad.1.9.973.
Human (HeLa) cells contain a protein, MLTF, which specifically binds to a DNA sequence in the adenovirus 2 major late promoter and activates transcription of that promoter. The presence of MLTF in uninfected cells suggests that this factor contributes to the transcription of some cellular genes. We find that MLTF binds in a sequence-specific manner to the 5'-flanking region of the mouse metallothionein I (mMTI) gene. Binding was localized between -101 and -94 (relative to the initiation site at +1) by DNA-binding gel electrophoresis assay and DNA methylation interference analysis. As in adenovirus, binding occurred in a region containing the sequence CPuCGTGAC. Deletion of this sequence both eliminated the binding of MLTF and produced a fourfold reduction in transcriptional efficiency in vitro. In contrast to the intact promoter, transcription from the deletion mutant promoter was not stimulated by addition of purified MLTF to an in vitro reconstituted reaction. These results suggest that MLTF contributes to the transcription of cellular genes.
人类(HeLa)细胞含有一种蛋白质,即MLTF,它能特异性地结合腺病毒2型主要晚期启动子中的一段DNA序列,并激活该启动子的转录。未感染细胞中存在MLTF,这表明该因子有助于某些细胞基因的转录。我们发现,MLTF以序列特异性的方式结合到小鼠金属硫蛋白I(mMTI)基因的5'侧翼区域。通过DNA结合凝胶电泳分析和DNA甲基化干扰分析,结合位点定位在-101至-94之间(相对于+1处的起始位点)。与腺病毒中一样,结合发生在包含序列CPuCGTGAC的区域。删除该序列既消除了MLTF的结合,又使体外转录效率降低了四倍。与完整启动子相反,向体外重组反应中添加纯化的MLTF并不能刺激缺失突变启动子的转录。这些结果表明,MLTF有助于细胞基因的转录。