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The cullin Rtt101 promotes ubiquitin-dependent DNA-protein crosslink repair across the cell cycle.

Audrey NoireterreJulien SoudetIvona BagdiulFrançoise Stutz
Published in: Nucleic acids research (2024)
DNA-protein crosslinks (DPCs) challenge faithful DNA replication and smooth passage of genomic information. Our study unveils the cullin E3 ubiquitin ligase Rtt101 as a DPC repair factor. Genetic analyses demonstrate that Rtt101 is essential for resistance to a wide range of DPC types including topoisomerase 1 crosslinks, in the same pathway as the ubiquitin-dependent aspartic protease Ddi1. Using an in vivo inducible Top1-mimicking DPC system, we reveal the significant impact of Rtt101 ubiquitination on DPC removal across different cell cycle phases. High-throughput methods coupled with next-generation sequencing specifically highlight the association of Rtt101 with replisomes as well as colocalization with DPCs. Our findings establish Rtt101 as a main contributor to DPC repair throughout the yeast cell cycle.
Keyphrases
  • cell cycle
  • cell proliferation
  • circulating tumor
  • high throughput
  • copy number
  • single molecule
  • cell free
  • genome wide
  • small molecule
  • single cell
  • healthcare
  • dna methylation
  • gene expression
  • circulating tumor cells