AI Article Synopsis

  • SUMO and ubiquitin are crucial for how cells respond to DNA damage, with Rnf4 acting as a link between these two processes.
  • Rnf4 transfers ubiquitin to substrates modified by SUMO and can interact with various E2 enzymes, like Ube2w.
  • In chicken and human cells, Rnf4 depletion increases sensitivity to DNA-damaging agents, while removing Ube2w alone doesn’t affect this response; however, Ube2w becomes harmful without Rnf4, suggesting they operate in separate pathways during DNA damage response.

Article Abstract

SUMO and ubiquitin play important roles in the response of cells to DNA damage. These pathways are linked by the SUMO Targeted ubiquitin Ligase Rnf4 that catalyses transfer of ubiquitin from a ubiquitin loaded E2 conjugating enzyme to a polySUMO modified substrate. Rnf4 can functionally interact with multiple E2s, including Ube2w, in vitro. Chicken cells lacking Rnf4 are hypersensitive to hyroxyurea, DNA alkylating drugs and DNA crosslinking agents, but this sensitivity is suppressed by simultaneous depletion of Ube2w. Cells depleted of Ube2w alone are not hypersensitive to the same DNA damaging agents. Similar results were also obtained in human cells. These data indicate that Ube2w does not have an essential role in the DNA damage response, but is deleterious in the absence of Rnf4. Thus, although Rnf4 and Ube2w functionally interact in vitro, our genetic experiments indicate that in response to DNA damage Ube2w and Rnf4 function in distinct pathways.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868978PMC
http://dx.doi.org/10.1038/srep26178DOI Listing

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