RNAPII-dependent ATM signaling at collisions with replication forks

Elias Einig, Chao Jin, Valentina Andrioletti, Boris Macek and Nikita Popov ()
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Elias Einig: University Hospital Tübingen
Chao Jin: University Hospital Tübingen
Valentina Andrioletti: University Hospital Tübingen
Boris Macek: Eberhard Karls University of Tübingen
Nikita Popov: University Hospital Tübingen

Nature Communications, 2023, vol. 14, issue 1, 1-17

Abstract: Abstract Deregulation of RNA Polymerase II (RNAPII) by oncogenic signaling leads to collisions of RNAPII with DNA synthesis machinery (transcription-replication conflicts, TRCs). TRCs can result in DNA damage and are thought to underlie genomic instability in tumor cells. Here we provide evidence that elongating RNAPII nucleates activation of the ATM kinase at TRCs to stimulate DNA repair. We show the ATPase WRNIP1 associates with RNAPII and limits ATM activation during unperturbed cell cycle. WRNIP1 binding to elongating RNAPII requires catalytic activity of the ubiquitin ligase HUWE1. Mutation of HUWE1 induces TRCs, promotes WRNIP1 dissociation from RNAPII and binding to the replisome, stimulating ATM recruitment and activation at RNAPII. TRCs and translocation of WRNIP1 are rapidly induced in response to hydroxyurea treatment to activate ATM and facilitate subsequent DNA repair. We propose that TRCs can provide a controlled mechanism for stalling of replication forks and ATM activation, instrumental in cellular response to replicative stress.

Date: 2023
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DOI: 10.1038/s41467-023-40924-4

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