CTDP1 and RPB7 stabilize Pol II and permit reinitiation
Haonan Zheng1, Qiqin Xu1, Dexun Ji1
1State Key Laboratory of Gene Function and Modulation Research, Key Laboratory of Cell Proliferation and Differentiation of the Ministry of Education, Beijing Advanced Center of RNA Biology (BEACON), School of Life Sciences, Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, China.
Abstract:
The mechanisms governing the termination and subsequent reinitiation of RNA polymerase II (Pol II) remain poorly understood. Here we find that depletion of RPB7 leads to the destabilization of Pol II's largest subunit, RPB1. This destabilization is influenced by the loop regions of RPB7, CDK9, the C-terminal domain (CTD) of RPB1, and its linker region. The stabilization process of RPB1 is regulated by the E3 ubiquitin ligase Cullin 3. Additionally, RPB7 interacts with the phosphatase CTDP1, which is crucial for maintaining RPB1 stability. RPB7 is also vital for the reinitiation of Pol II, engages with RNA processing factors, and is localized to the RNA exit channel of the Pol II complex. The absence of RPB7 compromises RNA processing. We propose that RPB7 recruits CTDP1 to dephosphorylate Pol II, enhancing its stability and facilitating efficient reinitiation, adding an emerging dimension to transcriptional regulation.
Related Concept Videos
Restarting Stalled Replication Forks
DNA Damage can Stall the Cell Cycle
Transcription Initiation
The promoters and enhancers and their accessory proteins allow tight regulation of...
Translesion DNA Polymerases
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
Eukaryotic RNA Polymerases
All three eukaryotic RNAPs require specific transcription factors, of which the...
Negative Regulator Molecules


