Chung C N, Hamaguchi Y, Honjo T, Kawaichi M
Department of Medical Chemistry, Kyoto University Faculty of Medicine, Japan.
Nucleic Acids Res. 1994 Aug 11;22(15):2938-44. doi: 10.1093/nar/22.15.2938.
To map regions important for DNA binding of the mouse homologue of Suppressor of Hairless or RBP-J kappa protein, mutated mouse RBP-J kappa cDNAs were made by insertion of oligonucleotide linkers or base replacement. DNA binding assays using the mutated proteins expressed in COS cells showed that various mutations between 218 Arg and 227 Arg decreased the DNA binding activity drastically. The DNA binding activity was not affected by amino acid replacements within the integrase motif of the RBP-J kappa protein (230His-269His). Replacements between 291Arg and 323Tyr affected the DNA binding activity slightly but reproducibly. These results indicate that the region encompassing 218Arg-227Arg is critical for the DNA binding activity of RBP-J kappa. This region did not show any significant homology to motifs or domains of the previously described DNA binding proteins. Using a truncation mutant protein RBP-J kappa was shown to associate with DNA as a monomer.
为了绘制对无毛抑制因子或RBP-Jκ蛋白的小鼠同源物的DNA结合重要的区域,通过插入寡核苷酸接头或碱基置换制备了突变的小鼠RBP-Jκ cDNA。使用在COS细胞中表达的突变蛋白进行的DNA结合试验表明,218位精氨酸和227位精氨酸之间的各种突变显著降低了DNA结合活性。DNA结合活性不受RBP-Jκ蛋白整合酶基序(230位组氨酸-269位组氨酸)内氨基酸置换的影响。291位精氨酸和323位酪氨酸之间的置换对DNA结合活性有轻微但可重复的影响。这些结果表明,包含218位精氨酸-227位精氨酸的区域对RBP-Jκ的DNA结合活性至关重要。该区域与先前描述的DNA结合蛋白的基序或结构域没有任何显著同源性。使用截短突变蛋白表明RBP-Jκ以单体形式与DNA结合。