State Key Laboratory of Oncogenes and Related Genes, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Institute of Precision Medicine, Shanghai, China.
Nat Struct Mol Biol. 2021 Feb;28(2):220-227. doi: 10.1038/s41594-021-00557-x. Epub 2021 Feb 8.
RNA polymerase III (Pol III) synthesizes structured, essential small RNAs, such as transfer RNA, 5S ribosomal RNA and U6 small nuclear RNA. Pol III, the largest nuclear RNA polymerase, is composed of a conserved core region and eight constitutive regulatory subunits, but how these factors jointly regulate Pol III transcription remains unclear. Here, we present cryo-EM structures of human Pol III in both apo and elongating states, which unveil both an orchestrated movement during the apo-to-elongating transition and an unexpected apo state in which the RPC7 subunit tail occupies the DNA-RNA-binding cleft of Pol III, suggesting that RPC7 plays important roles in both autoinhibition and transcription initiation. The structures also reveal a proofreading mechanism for the TFIIS-like subunit RPC10, which stably retains its catalytic position in the secondary channel, explaining the high fidelity of Pol III transcription. Our work provides an integrated picture of the mechanism of Pol III transcription regulation.
RNA 聚合酶 III(Pol III)合成结构必需的小 RNA,如转移 RNA、5S 核糖体 RNA 和 U6 小核 RNA。Pol III 是最大的核 RNA 聚合酶,由保守的核心区域和八个组成型调节亚基组成,但这些因素如何共同调节 Pol III 转录仍不清楚。在这里,我们展示了人源 Pol III 在apo 和延伸状态下的冷冻电镜结构,揭示了 apo 到延伸转变过程中的协调运动以及出人意料的 apo 状态,在这种状态下,RPC7 亚基尾部占据 Pol III 的 DNA-RNA 结合裂隙,表明 RPC7 在自动抑制和转录起始中都发挥重要作用。这些结构还揭示了 TFIIS 样亚基 RPC10 的校对机制,RPC10 稳定地保留在二级通道中的催化位置,解释了 Pol III 转录的高保真度。我们的工作提供了 Pol III 转录调控机制的综合图景。