German Center for Neurodegenerative Diseases (DZNE), Von-Siebold Straße 3A, D-35075 Göttingen, Germany.
Department of NMR-based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Am Faßberg 11, D-37077 Göttingen, Germany.
Biol Chem. 2023 Jun 20;404(8-9):839-844. doi: 10.1515/hsz-2023-0136. Print 2023 Jul 26.
The repetitive heptads in the C-terminal domain (CTD) of RPB1, the largest subunit of RNA Polymerase II (Pol II), play a critical role in the regulation of Pol II-based transcription. Recent findings on the structure of the CTD in the pre-initiation complex determined by cryo-EM and the novel phase separation properties of key transcription components offers an expanded mechanistic interpretation of the spatiotemporal distribution of Pol II during transcription. Current experimental evidence further suggests an exquisite balance between CTD's local structure and an array of multivalent interactions that drive phase separation of Pol II and thus shape its transcriptional activity.
RNA 聚合酶 II(Pol II)大亚基 RPB1 的 C 端结构域(CTD)中的重复七肽在 Pol II 依赖的转录调控中起着关键作用。最近通过 cryo-EM 确定的起始前复合物中 CTD 的结构以及关键转录成分的新型相分离特性为 Pol II 在转录过程中的时空分布提供了扩展的机制解释。目前的实验证据进一步表明,CTD 的局部结构与一系列多价相互作用之间存在着微妙的平衡,这些相互作用驱动 Pol II 的相分离,从而塑造其转录活性。