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Much of this work is focused on how the DDR is controlled by protein post-translational modifications (PTMs; 2). (2014) Systematic characterization of deubiquitylating enzymes for roles in maintaining genome integrity.
For example, we have established that the mammalian SUMO E3 ligases PIAS1 and PIAS4 accumulate at DSB sites and promote cellular responses to DNA double strand breaks (DSBs) by mediating SUMOylation of various DDR factors (3). Davies OR*, Forment JV*, Sun M, Belotserkovskaya R, Coates J, Galanty Y, Demir M, Morton CR, Rzechorzek NJ, Jackson SP^, Pellegrini L^.
Furthermore, we recently discovered that the histone deacetylase enzymes HDAC1 and HDAC2 accumulate at DSB sites to facilitate repair by non-homologous end-joining (4). (2015) Ct IP tetramer assembly is required for DNA-end resection and repair.
Our current work is geared towards further defining the mechanisms of the DDR particularly within the context of chromatin, and the role that PTMs have in controlling this key biological response.
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Our work focuses on the DNA damage response (DDR): the set of events that optimises cell survival by detecting DNA damage, signalling its presence and mediating its repair.
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