Shanghai Fifth People's Hospital, Fudan University, and Shanghai Key Laboratory of Medical Epigenetics, International Co-laboratory of Medical Epigenetics and Metabolism (Ministry of Science and Technology), Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China.
Nucleic Acids Res. 2024 Nov 27;52(21):12767-12783. doi: 10.1093/nar/gkae787.
Transcription-coupled repair (TCR) is the major pathway to remove transcription-blocking lesions. Although discovered for nearly 40 years, the mechanism and critical players of mammalian TCR remain unclear. STK19 is a factor affecting cell survival and recovery of RNA synthesis in response to DNA damage, however, whether it is a necessary component for TCR is unknown. Here, we demonstrated that STK19 is essential for human TCR. Mechanistically, STK19 is recruited to damage sites through direct interaction with CSA. It can also interact with RNA polymerase II in vitro. Once recruited, STK19 plays an important role in UVSSA ubiquitination which is needed for TCR. STK19 also promotes TCR independent of UVSSA ubiquitination by stimulating TFIIH recruitment through its direct interaction with TFIIH. In summary, our results suggest that STK19 is a key factor of human TCR that links CSA, UVSSA ubiquitination and TFIIH loading, shedding light on the molecular mechanisms of TCR.
转录偶联修复(TCR)是去除转录阻断损伤的主要途径。尽管 TCR 的发现已经近 40 年,但哺乳动物 TCR 的机制和关键成分仍不清楚。STK19 是一个影响细胞存活和 RNA 合成恢复的因子,以响应 DNA 损伤,然而,它是否是 TCR 的必要组成部分尚不清楚。在这里,我们证明了 STK19 对人类 TCR 是必不可少的。从机制上讲,STK19 通过与 CSA 的直接相互作用被招募到损伤部位。它还可以在体外与 RNA 聚合酶 II 相互作用。一旦被招募,STK19 在 TCR 所必需的 UVSSA 泛素化中发挥重要作用。STK19 还通过其与 TFIIH 的直接相互作用刺激 TFIIH 的募集,从而促进 TCR 的发生,而不依赖于 UVSSA 泛素化。总之,我们的结果表明,STK19 是人类 TCR 的关键因素,它连接 CSA、UVSSA 泛素化和 TFIIH 加载,为 TCR 的分子机制提供了线索。