4.8 Article

Inhibition of Homologous Recombination by the PCNA-Interacting Protein PARI

Journal

MOLECULAR CELL
Volume 45, Issue 1, Pages 75-86

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2011.11.010

Keywords

-

Funding

  1. International Human Frontiers Science Program
  2. Susan G. Komen Breast Cancer Foundation
  3. National Institutes of Health [R01DK43889, R01HL52725, P01HL048546, P01CA092584]
  4. Deutsche Forschungsgemeinschaft [SPP1365]
  5. Cancer Research UK [11581] Funding Source: researchfish
  6. Grants-in-Aid for Scientific Research [23221005] Funding Source: KAKEN

Ask authors/readers for more resources

Inappropriate homologous recombination (HR) causes genomic instability and cancer. In yeast, the UvrD family helicase Srs2 is recruited to sites of DNA replication by SUMO-modified PCNA, where it acts to restrict HR by disassembling toxic RAD51 nucleofilaments. How human cells control recombination at replication forks is unknown. Here, we report that the protein PARI, containing a UvrD-like helicase domain, is a PCNA-interacting partner required for preservation of genome stability in human and DT40 chicken cells. Using cell-based and biochemical assays, we show that PARI restricts unscheduled recombination by interfering with the formation of RAD51-DNA HR structures. Finally, we show that PARI knockdown suppresses the genomic instability of Fanconi Anemia/BRCA pathway-deficient cells. Thus, we propose that PARI is a long sought-after factor that suppresses inappropriate recombination events at mammalian replication forks.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available