RIKEN Center for Life Science Technologies, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan.
RIKEN Structural Biology Laboratory, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan.
Science. 2017 Sep 1;357(6354):921-924. doi: 10.1126/science.aan8552. Epub 2017 Aug 3.
In the early stage of transcription, eukaryotic RNA polymerase II (Pol II) exchanges initiation factors with elongation factors to form an elongation complex for processive transcription. Here we report the structure of the Pol II elongation complex bound with the basal elongation factors Spt4/5, Elf1, and TFIIS. Spt4/5 (the Spt4/Spt5 complex) and Elf1 modify a wide area of the Pol II surface. Elf1 bridges the Pol II central cleft, completing a "DNA entry tunnel" for downstream DNA. Spt4 and the Spt5 NGN and KOW1 domains encircle the upstream DNA, constituting a "DNA exit tunnel." The Spt5 KOW4 and KOW5 domains augment the "RNA exit tunnel," directing the exiting nascent RNA. Thus, the elongation complex establishes a completely different transcription and regulation platform from that of the initiation complexes.
在转录的早期阶段,真核 RNA 聚合酶 II(Pol II)与延伸因子交换起始因子,以形成用于连续转录的延伸复合物。在这里,我们报告了与基础延伸因子 Spt4/5、Elf1 和 TFIIS 结合的 Pol II 延伸复合物的结构。Spt4/5(Spt4/Spt5 复合物)和 Elf1 修饰了 Pol II 表面的广泛区域。Elf1 桥接了 Pol II 的中央裂隙,为下游 DNA 完成了“DNA 进入隧道”。Spt4 和 Spt5 的 NGN 和 KOW1 结构域环绕上游 DNA,构成了“DNA 出口隧道”。Spt5 的 KOW4 和 KOW5 结构域增加了“RNA 出口隧道”,指导新生 RNA 的排出。因此,延伸复合物建立了一个与起始复合物完全不同的转录和调控平台。