Bukenberger M, Marschalek R, Salzburger W, Dingermann T
Institut für Biochemie der Medizinischen Fakultät, Universität Erlangen-Nürnberg, Federal Republic of Germany.
Curr Genet. 1991 Jul;20(1-2):129-35. doi: 10.1007/BF00312775.
RNA Polymerase III transcription factors from the cellular slime mold Dictyostelium discoideum were characterized, based on their stable binding to isolated tRNA genes. Different protein complexes are sequestered on DNA fragments containing tRNA genes depending on the conditions by which the nuclei were extracted. Binding specificity was determined through competition assays using competitor tRNA genes from the same gene family, from different gene families and from truncated tRNA genes. The complex with the highest multiformity of interdependent proteins is able to assemble with low affinity on a B-block-free tDNA template, whereas most lower molecular weight complexes require the presence of an intact B-block promoter element in order to assemble.
基于它们与分离的tRNA基因的稳定结合,对来自细胞黏菌盘基网柄菌的RNA聚合酶III转录因子进行了表征。根据提取细胞核的条件,不同的蛋白质复合物被隔离在含有tRNA基因的DNA片段上。通过使用来自同一基因家族、不同基因家族和截短tRNA基因的竞争tRNA基因进行竞争试验来确定结合特异性。具有最高相互依赖蛋白质多样性的复合物能够以低亲和力在无B块的tDNA模板上组装,而大多数较低分子量的复合物需要完整的B块启动子元件才能组装。