Molecular model of TFIIH recruitment to the transcription-coupled repair machinery

Tanmoy Paul, Chunli Yan, Jina Yu, Susan E. Tsutakawa, John A. Tainer, Dong Wang and Ivaylo Ivanov ()
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Tanmoy Paul: Georgia State University
Chunli Yan: Georgia State University
Jina Yu: Georgia State University
Susan E. Tsutakawa: Lawrence Berkeley National Laboratory
John A. Tainer: Lawrence Berkeley National Laboratory
Dong Wang: University of California
Ivaylo Ivanov: Georgia State University

Nature Communications, 2025, vol. 16, issue 1, 1-17

Abstract: Abstract Transcription-coupled repair (TCR) is a vital nucleotide excision repair sub-pathway that removes DNA lesions from actively transcribed DNA strands. Binding of CSB to lesion-stalled RNA Polymerase II (Pol II) initiates TCR by triggering the recruitment of downstream repair factors. Yet it remains unknown how transcription factor IIH (TFIIH) is recruited to the intact TCR complex. Combining existing structural data with AlphaFold predictions, we build an integrative model of the initial TFIIH-bound TCR complex. We show how TFIIH can be first recruited in an open repair-inhibited conformation, which requires subsequent CAK module removal and conformational closure to process damaged DNA. In our model, CSB, CSA, UVSSA, elongation factor 1 (ELOF1), and specific Pol II and UVSSA-bound ubiquitin moieties come together to provide interaction interfaces needed for TFIIH recruitment. STK19 acts as a linchpin of the assembly, orienting the incoming TFIIH and bridging Pol II to core TCR factors and DNA. Molecular simulations of the TCR-associated CRL4CSA ubiquitin ligase complex unveil the interplay of segmental DDB1 flexibility, continuous Cullin4A flexibility, and the key role of ELOF1 for Pol II ubiquitination that enables TCR. Collectively, these findings elucidate the coordinated assembly of repair proteins in early TCR.

Date: 2025
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DOI: 10.1038/s41467-025-57593-0

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