Chu W M, Wang Z, Roeder R G, Schmid C W
Section of Molecular and Cellular Biology, University of California, Davis, Davis, California 95616, USA.
J Biol Chem. 1997 Jun 6;272(23):14755-61. doi: 10.1074/jbc.272.23.14755.
The retinoblastoma susceptibility gene product (Rb) generally represses RNA polymerase III (Pol III)-directed transcription. This implies that Rb interacts with essential transcription factors. Mutations in either the A or B subdomains in the Rb pocket interfere with Rb-mediated repression of Pol III-directed transcription, which indicates that both subdomains are directly involved in this activity. Addition of either purified TFIIIB or purified TFIIIC2 partially relieves Rb-mediated repression and restores activity to nuclear extracts that had been depleted of essential factors by binding to Rb. Pull down and coimmunoprecipitation experiments as well as functional assays indicate that Rb interacts with both TFIIIB and TFIIIC2 and that the A subdomain is primarily required for binding TFIIIB and the B subdomain for binding TFIIIC2. While Rb interacts with both factors, the A subdomain is more important than the B subdomain in directing Rb-mediated repression, and TFIIIB is the principal target of that activity.
视网膜母细胞瘤易感基因产物(Rb)通常会抑制RNA聚合酶III(Pol III)介导的转录。这意味着Rb与必需的转录因子相互作用。Rb口袋中A或B亚结构域的突变会干扰Rb介导的对Pol III介导转录的抑制,这表明这两个亚结构域都直接参与了该活性。添加纯化的TFIIIB或纯化的TFIIIC2可部分缓解Rb介导的抑制作用,并使因与Rb结合而耗尽必需因子的核提取物恢复活性。下拉实验、共免疫沉淀实验以及功能分析表明,Rb与TFIIIB和TFIIIC2都相互作用,并且A亚结构域主要是与TFIIIB结合所必需的,而B亚结构域是与TFIIIC2结合所必需的。虽然Rb与这两种因子都相互作用,但在指导Rb介导的抑制作用方面,A亚结构域比B亚结构域更重要,并且TFIIIB是该活性的主要靶点。