1. Elf1 promotes Rad26s interaction with lesion-arrested Pol II for transcription-coupled repair.
- Author
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Sarsam, Reta, Xu, Jun, Lahiri, Indrajit, Gong, Wenzhi, Li, Qingrong, Oh, Juntaek, Zhou, Zhen, Hou, Peini, Chong, Jenny, Hao, Nan, Li, Shisheng, Leschziner, Andres, and Wang, Dong
- Subjects
Cockayne syndrome B ,Elf1 ,RNA polymerase II ,cryo-EM ,transcription-coupled repair ,Humans ,Cognition ,DNA Damage ,Excision Repair ,Heart Arrest ,RNA Polymerase II ,Saccharomyces cerevisiae - Abstract
Transcription-coupled nucleotide excision repair (TC-NER) is a highly conserved DNA repair pathway that removes bulky lesions in the transcribed genome. Cockayne syndrome B protein (CSB), or its yeast ortholog Rad26, has been known for decades to play important roles in the lesion-recognition steps of TC-NER. Another conserved protein ELOF1, or its yeast ortholog Elf1, was recently identified as a core transcription-coupled repair factor. How Rad26 distinguishes between RNA polymerase II (Pol II) stalled at a DNA lesion or other obstacles and what role Elf1 plays in this process remains unknown. Here, we present cryo-EM structures of Pol II-Rad26 complexes stalled at different obstacles that show that Rad26 uses a common mechanism to recognize a stalled Pol II, with additional interactions when Pol II is arrested at a lesion. A cryo-EM structure of lesion-arrested Pol II-Rad26 bound to Elf1 revealed that Elf1 induces further interactions between Rad26 and a lesion-arrested Pol II. Biochemical and genetic data support the importance of the interplay between Elf1 and Rad26 in TC-NER initiation. Together, our results provide important mechanistic insights into how two conserved transcription-coupled repair factors, Rad26/CSB and Elf1/ELOF1, work together at the initial lesion recognition steps of transcription-coupled repair.
- Published
- 2024