Poly(ADP-ribose)-binding promotes Exo1 damage recruitment and suppresses its nuclease activities

Abigael Cheruiyot, Sharad C. Paudyal, In Kwon Kim, Melanie Sparks, Tom Ellenberger, Helen Piwnica-Worms, Zhongsheng You

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Exonuclease 1 (Exo1) has important roles in DNA metabolic transactions that are essential for genome maintenance, telomere regulation and cancer suppression. However, the mechanisms for regulating Exo1 activity in these processes remain incompletely understood. Here, we report that Exo1 activity is regulated by a direct interaction with poly(ADP-ribose) (PAR), a prominent posttranslational modification at the sites of DNA damage. This PAR-binding activity promotes the early recruitment of Exo1 to sites of DNA damage, where it is retained through an interaction with PCNA, which interacts with the C-terminus of Exo1. The effects of both PAR and PCNA on Exo1 damage association are antagonized by the 14-3-3 adaptor proteins, which interact with the central domain of Exo1. Although PAR binding inhibits both the exonuclease activity and the 5' flap endonuclease activity of purified Exo1, the pharmacological blockade of PAR synthesis does not overtly affect DNA double-strand break end resection in a cell free Xenopus egg extract. Thus, the counteracting effects of PAR on Exo1 recruitment and enzymatic activity may enable appropriate resection of DNA ends while preventing unscheduled or improper processing of DNA breaks in cells.

Original languageEnglish
Pages (from-to)106-115
Number of pages10
JournalDNA Repair
Volume35
DOIs
StatePublished - Nov 1 2015

Keywords

  • 14-3-3
  • DNA end resection
  • DNA replication
  • Exo1
  • PCNA
  • Poly(ADP-ribosyl)ation

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