Dana A. D’Orlando

ORCID: 0009-0005-3404-0769
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About
Contact & Profiles
Research Areas
  • DNA Repair Mechanisms
  • Ubiquitin and proteasome pathways
  • RNA modifications and cancer
  • Autophagy in Disease and Therapy
  • Chromosomal and Genetic Variations
  • Streptococcal Infections and Treatments
  • Genomics and Chromatin Dynamics
  • Inflammasome and immune disorders

National Institutes of Health
2023

Case Western Reserve University
2023

The Y-family DNA polymerases – Pol ι, η, κ and Rev1 are most well-known for their roles in the damage tolerance pathway of translesion synthesis (TLS). They function to overcome replication barriers by bypassing lesions that cannot be normally replicated, allowing forks continue without stalling. In this work, we demonstrate a novel interaction between each polymerase nucleotide excision repair (NER) proteins, RAD23A RAD23B. We initially focus on through series biochemical, cell-based,...

10.1016/j.jmb.2023.168353 article EN cc-by-nc-nd Journal of Molecular Biology 2023-11-05

DNA polymerase eta (Pol η) is a Y-family translesion responsible for synthesizing new across UV-damaged templates. It recruited to replication forks following mono-ubiquitination of the PCNA clamp. This interaction mediated by PCNA-interacting protein (PIP) motifs within Pol η, as well its C-terminal ubiquitin-binding zinc finger (UBZ) domain. Previous work has suggested that η itself mono-ubiquitinated at four lysine residues, which dependent on prior UBZ Here, we show can be modified same...

10.1101/2024.10.12.618026 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-10-13
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