Galson D L, Housman D E
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Mol Cell Biol. 1988 Jan;8(1):381-92. doi: 10.1128/mcb.8.1.381-392.1988.
To identify proteins from uninduced murine erythroleukemia nuclear extracts which specifically bind to sequences from the DNase I-hypersensitive region within the mouse beta-globin intervening sequence 2 (IVS2), a gel electrophoretic mobility shift assay was used. Two distinct sequence-specific binding proteins were detected. The specific binding sites for these factors were delineated by both DNase I protection footprinting and methylation interference. Factor B1 bound specifically to two homologous sites, B1-A and B1-B, approximately 100 base pairs apart within the IVS2 and on opposite strands. These two regions could interact with factor B1 independently. Factor B1 was limited to cells of hematopoietic lineages. Factor B2 bound to a site approximately 5 base pairs away from the B1-A site and was limited to cells of the erythroid lineage. The limited tissue distribution of these factors and the locations of their binding sites suggest that one or both of these factors may be involved in the formation of the tissue-specific DNase I-hypersensitive site in the IVS2 of the mouse beta-globin gene.
为了从小鼠红白血病细胞核提取物中鉴定出能特异性结合小鼠β-珠蛋白内含子2(IVS2)中DNase I高敏区域序列的蛋白质,我们采用了凝胶电泳迁移率变动分析。检测到了两种不同的序列特异性结合蛋白。通过DNase I保护足迹法和甲基化干扰法确定了这些因子的特异性结合位点。因子B1特异性结合IVS2内两条相反链上相距约100个碱基对的两个同源位点B1-A和B1-B。这两个区域可独立与因子B1相互作用。因子B1局限于造血谱系的细胞。因子B2结合在距B1-A位点约5个碱基对的位置,且局限于红系谱系的细胞。这些因子有限的组织分布及其结合位点的位置表明,这些因子中的一个或两个可能参与了小鼠β-珠蛋白基因IVS2中组织特异性DNase I高敏位点的形成。