USP50 suppresses alternative RecQ helicase use and deleterious DNA2 activity during replication

• Published in: bioRxiv
• Main Authors: Mackay, Hannah L, Stone, Helen R, Ellis, Katherine, Ronson, George E, Walker, Alexandra K, Starowicz, Katarzyna, Garvin, Alexander J, van Eijk, Patrick, Vaitsiankova, Alina, Vijayendran, Sobana, Beesley, James F, Petermann, Eva, Brown, Eric J, Densham, Ruth M, Reed, Simon H, Dobbs, Felix, Saponaro, Marco, Morris, Joanna R
• Format: Journal Article
• Language: English
• Published: United States 11.01.2024
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2024.01.10.574674

Mammalian DNA replication employs several RecQ DNA helicases to orchestrate the faithful duplication of genetic information. Helicase function is often coupled to the activity of specific nucleases, but how helicase and nuclease activities are co-directed is unclear. Here we identify the inactive ubiquitin-specific protease, USP50, as a ubiquitin-binding and chromatin-associated protein required for ongoing replication, fork restart, telomere maintenance and cellular survival during replicative stress. USP50 supports WRN:FEN1 at stalled replication forks, suppresses MUS81-dependent fork collapse and restricts double-strand DNA breaks at GC-rich sequences. Surprisingly we find that cells depleted for USP50 and recovering from a replication block exhibit increased DNA2 and RECQL4 foci and that the defects in ongoing replication, poor fork restart and increased fork collapse seen in these cells are mediated by DNA2, RECQL4 and RECQL5. These data define a novel ubiquitin-dependent pathway that promotes the balance of helicase: nuclease use at ongoing and stalled replication forks.