Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735898
Title: Characterization of UHRF2 (RNF107) as a novel sensor for DNA ICLs in the Fanconi Anemia pathway
Author: Motnenko, Anna
ISNI:       0000 0004 6500 6366
Awarding Body: University of Oxford
Current Institution: University of Oxford
Date of Award: 2017
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Abstract:
The Fanconi Anemia (FA) pathway is important for repairing interstrand crosslinks (ICLs) between the Watson-Crick strands of the DNA helix. An initial and essential stage in the repair process is the detection of the ICL. In a previous study, UHRF1 was identified as an ICL sensor in humans, it was shown that downstream repair factors were not recruited normally to the ICL in the absence of UHRF1. However, the mechanism underlying this process was unknown. Here, we report the identification of UHRF2, a paralogue of UHRF1, as an ICL sensor protein. We show that UHRF2 cooperates with UHRF1, to ensure recruitment of FANCD2 to the ICL. We show that a direct protein-protein interaction with FANCD2 is formed via the SRA domain of UHRF1, and a direct interaction is formed between UHRF2 and UHRF1. Moreover, we demonstrate that the essential monoubiquitination of FANCD2 is stimulated by UHRF1/UHRF2, by mediating its retention on chromatin. Taken together, we uncover the mechanism of FANCD2 activation by monoubiquitination via recruitment and retention at ICLs dependent on an interaction with UHRF1/UHRF2.
Supervisor: Cohn, Martin A. Sponsor: Natural Sciences and Engineering Research Council of Canada (NSERC)
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.735898  DOI: Not available
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