Miwa T, Boxer L M, Kedes L
MEDIGEN Project, Department of Medicine, Stanford University School of Medicine, Palo Alto, CA.
Proc Natl Acad Sci U S A. 1987 Oct;84(19):6702-6. doi: 10.1073/pnas.84.19.6702.
Positively acting, rate-limiting regulatory factors that influence tissue-specific expression of the human cardiac alpha-actin gene in a mouse muscle cell line are shown by in vivo competition and gel mobility-shift assays to bind to upstream regions of its promoter but to neither vector DNA nor a beta-globin promoter. Although the two binding regions are distinctly separated, each corresponds to a cis region required for muscle-specific transcriptional stimulation, and each contains a core CC(A + T-rich)6GG sequence (designated CArG box), which is found in the promoter regions of several muscle-associated genes. Each site has an apparently different binding affinity for trans-acting factors, which may explain the different transcriptional stimulation activities of the two cis regions. Therefore, we conclude that the two CArG box regions are responsible for muscle-specific transcriptional activity of the cardiac alpha-actin gene through a mechanism that involves their binding of a positive trans-acting factor in muscle cells.
通过体内竞争和凝胶迁移率变动分析表明,在小鼠肌肉细胞系中影响人心肌α-肌动蛋白基因组织特异性表达的正向作用、限速调节因子可与该基因启动子的上游区域结合,但不与载体DNA或β-珠蛋白启动子结合。尽管两个结合区域明显分开,但每个区域都对应于肌肉特异性转录刺激所需的顺式区域,且每个区域都包含一个核心CC(A + T富集)6GG序列(称为CArG框),该序列存在于几个肌肉相关基因的启动子区域中。每个位点对反式作用因子具有明显不同的结合亲和力,这可能解释了两个顺式区域不同的转录刺激活性。因此,我们得出结论,两个CArG框区域通过涉及它们在肌肉细胞中与正向反式作用因子结合的机制,负责心肌α-肌动蛋白基因的肌肉特异性转录活性。