Structural basis of human transcription–DNA repair coupling

Goran Kokic, Felix R. Wagner, Aleksandar Chernev, Henning Urlaub and Patrick Cramer ()
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Goran Kokic: Max Planck Institute for Biophysical Chemistry
Felix R. Wagner: Max Planck Institute for Biophysical Chemistry
Aleksandar Chernev: Bioanalytical Mass Spectrometry
Henning Urlaub: Bioanalytical Mass Spectrometry
Patrick Cramer: Max Planck Institute for Biophysical Chemistry

Nature, 2021, vol. 598, issue 7880, 368-372

Abstract: Abstract Transcription-coupled DNA repair removes bulky DNA lesions from the genome1,2 and protects cells against ultraviolet (UV) irradiation3. Transcription-coupled DNA repair begins when RNA polymerase II (Pol II) stalls at a DNA lesion and recruits the Cockayne syndrome protein CSB, the E3 ubiquitin ligase, CRL4CSA and UV-stimulated scaffold protein A (UVSSA)3. Here we provide five high-resolution structures of Pol II transcription complexes containing human transcription-coupled DNA repair factors and the elongation factors PAF1 complex (PAF) and SPT6. Together with biochemical and published3,4 data, the structures provide a model for transcription–repair coupling. Stalling of Pol II at a DNA lesion triggers replacement of the elongation factor DSIF by CSB, which binds to PAF and moves upstream DNA to SPT6. The resulting elongation complex, ECTCR, uses the CSA-stimulated translocase activity of CSB to pull on upstream DNA and push Pol II forward. If the lesion cannot be bypassed, CRL4CSA spans over the Pol II clamp and ubiquitylates the RPB1 residue K1268, enabling recruitment of TFIIH to UVSSA and DNA repair. Conformational changes in CRL4CSA lead to ubiquitylation of CSB and to release of transcription-coupled DNA repair factors before transcription may continue over repaired DNA.

Date: 2021
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DOI: 10.1038/s41586-021-03906-4

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