Nature Communications (May 2017)

Molecular basis for PrimPol recruitment to replication forks by RPA

  • Thomas A. Guilliam,
  • Nigel C. Brissett,
  • Aaron Ehlinger,
  • Benjamin A. Keen,
  • Peter Kolesar,
  • Elaine M. Taylor,
  • Laura J. Bailey,
  • Howard D. Lindsay,
  • Walter J. Chazin,
  • Aidan J. Doherty

DOI
https://doi.org/10.1038/ncomms15222
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 14

Abstract

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PrimPol is a multifunctional replicative enzyme that can bypass DNA damage, as well as reprime replication restart. Here, the authors have elucidated how PrimPol is recruited to stalled replication forks via specific interactions with RPA, which stimulates its primase activity.