European Molecular Biology Laboratory, Structural and Computational Biology Unit, Heidelberg, Germany.
EMBO J. 2010 Nov 17;29(22):3762-72. doi: 10.1038/emboj.2010.266. Epub 2010 Oct 22.
RNA polymerase (Pol) III is responsible for the transcription of genes encoding small RNAs, including tRNA, 5S rRNA and U6 RNA. Here, we report the electron cryomicroscopy structures of yeast Pol III at 9.9 Å resolution and its elongation complex at 16.5 Å resolution. Particle sub-classification reveals prominent EM densities for the two Pol III-specific subcomplexes, C31/C82/C34 and C37/C53, that can be interpreted using homology models. While the winged-helix-containing C31/C82/C34 subcomplex initiates transcription from one side of the DNA-binding cleft, the C37/C53 subcomplex accesses the transcription bubble from the opposite side of this cleft. The transcribing Pol III enzyme structure not only shows the complete incoming DNA duplex, but also reveals the exit path of newly synthesized RNA. During transcriptional elongation, the Pol III-specific subcomplexes tightly enclose the incoming DNA duplex, which likely increases processivity and provides structural insights into the conformational switch between Pol III-mediated initiation and elongation.
RNA 聚合酶(Pol)III 负责转录编码小 RNA 的基因,包括 tRNA、5S rRNA 和 U6 RNA。在这里,我们报告了酵母 Pol III 在 9.9 Å 分辨率下的电子冷冻显微镜结构及其在 16.5 Å 分辨率下的延伸复合物结构。颗粒子分类揭示了两个 Pol III 特异性亚基 C31/C82/C34 和 C37/C53 的明显的 EM 密度,可以使用同源模型进行解释。虽然含有翼状螺旋的 C31/C82/C34 亚基从 DNA 结合裂隙的一侧起始转录,但是 C37/C53 亚基从该裂隙的另一侧进入转录泡。正在转录的 Pol III 酶结构不仅显示了完整的进入 DNA 双链,还揭示了新合成的 RNA 的出口路径。在转录延伸过程中,Pol III 特异性亚基紧密包围进入的 DNA 双链,这可能增加了 Pol III 介导的起始和延伸之间构象转换的连续性,并提供了结构见解。