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Assembly and isolation of intermediate steps of transcription complexes formed on the human 5S rRNA gene

机译:组装和分离人5S rRNA基因上形成的转录复合物的中间步骤

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摘要

By employing purified transcription factors and RNA polymerase III (pol III), we generated active pol III transcription complexes on the human 5S rRNA gene. These large complexes were separated by size exclusion chromatography from non- incorporated proteins. In addition, we succeeded in isolating specific intermediate stages of complex formation. Such isolated partial complexes require complementation with the missing activities for full transcription activity. One central finding is that a 5S DNA–TFIIIA–TFIIIC2–TFIIIBβ complex could be isolated which had been assembled in the absence of the general pol III transcription factor IIIC1. Thus TFIIIC1 is not an assembly factor for other transcription factors. Although pol III has the potential to bind unspecifically to DNA, such polymerase molecules cannot be rendered initiation competent by direct recruitment to a 5S DNA–TFIIIA–TFIIIC2– TFIIIBβ complex, but this process strictly requires additional TFIIIC1 activity. This clearly demonstrates that in contrast to yeast cells, hTFIIIB(β), although required, does not suffice for the functional recruitment of polymerase III. These data document that TFIIIC1 is the second transcription factor required for the recruitment of pol III in mammalian cells.
机译:通过采用纯化的转录因子和RNA聚合酶III(pol III),我们在人5S rRNA基因上产生了活性pol III转录复合物。通过尺寸排阻色谱法从未掺入的蛋白质中分离出这些大的复合物。此外,我们成功地分离了复杂形成的特定中间阶段。这种分离的部分复合物需要与缺失的活性互补以实现完整的转录活性。一个主要发现是,可以分离出5S DNA–TFIIIA–TFIIIC2–TFIIIBβ复合物,该复合物是在没有一般pol III转录因子IIIC1的情况下组装而成的。因此,TFIIIC1不是其他转录因子的装配因子。尽管pol III具有与DNA特异性结合的潜力,但不能通过直接募集5S DNA–TFIIIA–TFIIIC2–TFIIIBβ复合物来使此类聚合酶分子具有起始能力,但是此过程严格要求额外的TFIIIC1活性。这清楚地表明,与酵母细胞相比,hTFIIIB(β)尽管是必需的,但却不足以实现聚合酶III的功能募集。这些数据表明,TFIIIC1是在哺乳动物细胞中募集pol III所需的第二个转录因子。

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