Hatamochi A, Golumbek P T, Van Schaftingen E, de Crombrugghe B
Laboratory of Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892.
J Biol Chem. 1988 Apr 25;263(12):5940-7.
A CCAAT-binding activity present in nuclear extracts of rat liver and NIH 3T3 fibroblasts was purified using, as assay, DNA binding to a segment of the mouse alpha 2(I) collagen promoter. The activity consists of two components, designated factors A and B, which are separated by ion exchange chromatography on either Mono Q or Mono S columns. Factor A is heat-sensitive, whereas factor B is heat-resistant. Both factors are required for DNA binding and both are present in the DNA protein complex. The A + B complex was extensively purified by heparin-agarose and sequence-specific affinity chromatography. The Mr of factor A is 39,000, whereas the Mr of factor B is 41,000 as determined by renaturation of a highly purified preparation after sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Competition experiments indicate that this CCAAT-binding complex has a DNA sequence specificity that is different from those of other CCAAT-binding proteins.
利用与小鼠α2(I)胶原启动子片段的DNA结合作为检测方法,对大鼠肝脏和NIH 3T3成纤维细胞核提取物中存在的CCAAT结合活性进行了纯化。该活性由两个组分组成,分别命名为因子A和因子B,通过在Mono Q或Mono S柱上进行离子交换色谱分离。因子A对热敏感,而因子B耐热。DNA结合需要这两个因子,并且两者都存在于DNA-蛋白质复合物中。A + B复合物通过肝素-琼脂糖和序列特异性亲和色谱进行了广泛纯化。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后对高度纯化的制剂进行复性测定,因子A的Mr为39,000,而因子B的Mr为41,000。竞争实验表明,这种CCAAT结合复合物具有与其他CCAAT结合蛋白不同的DNA序列特异性。