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Detection of two tissue-specific DNA-binding proteins with affinity for sites in the mouse beta-globin intervening sequence 2.

机译:检测与小鼠β-珠蛋白干预序列2中的位点亲和的两种组织特异性DNA结合蛋白。

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摘要

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.
机译:为了从未诱导的鼠红细胞白血病核提取物中鉴定蛋白质,该蛋白质与小鼠β-珠蛋白干预序列2(IVS2)内DNase I超敏区域的序列特异性结合,使用了凝胶电泳迁移率变动分析法。检测到两种不同的序列特异性结合蛋白。 DNase I保护足迹和甲基化干扰都描述了这些因素的特异性结合位点。因子B1特异性结合两个同源位点B1-A和B1-B,分别位于IVS2内和相对链上约100个碱基对。这两个区域可以独立地与因子B1相互作用。因子B1限于造血谱系的细胞。因子B2与距B1-A位点约5个碱基对的位点结合,并限于红系谱系的细胞。这些因素的有限组织分布及其结合位点的位置表明,这些因素中的一个或两个都可能参与了小鼠β-珠蛋白基因的IVS2中组织特异性DNase I超敏感位点的形成。

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