• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107.

In all eukaryotes, the ligation of newly synthesized DNA, also known as Okazaki fragments, is catalysed by DNA ligase I (ref. 1). An individual with a DNA ligase I deficiency exhibits growth retardation, sunlight sensitivity and severe immunosuppression, probably due to accumulation of DNA damage. Surprisingly, not much is known about the DNA damage response (DDR) in DNA ligase I-deficient cells. As DNA replication and DDR pathways are highly conserved in eukaryotes, we used Saccharomyces cerevisiae as a model system to address this issue. We uncovered a new pathway, which facilitates ubiquitylation at Lys 107 of proliferating cell nuclear antigen (PCNA). Unlike ubiquitylation at Lys 164 of PCNA in response to UV irradiation, which triggers translesion synthesis, modification of Lys 107 is not dependent on the ubiquitin conjugating enzyme (E2) Rad6 (ref. 4) nor the ubiquitin ligase (E3) Rad18 (ref. 5), but requires the E2 variant Mms2 (ref. 6) in conjunction with Ubc4 (ref. 7) and the E3 Rad5 (Refs 8, 9). Surprisingly, DNA ligase I-deficient S. cerevisiae cdc9-1 cells that carry a PCNAK107R mutation are inviable, because they cannot activate a robust DDR. Furthermore, we show that ubiquitylation of PCNA in response to DNA ligase I deficiency is conserved in humans, yet the lysine residue that is modified remains to be determined. We propose that PCNA ubiquitylation provides a 'DNA damage code' that allows cells to categorize different types of defects that arise during DNA replication.

Pubmed ID: 20010813

Authors

  • Das-Bradoo S
  • Nguyen HD
  • Wood JL
  • Ricke RM
  • Haworth JC
  • Bielinsky AK

Journal

Nature cell biology

Publication Data

January 22, 2010

Associated Grants

  • Agency: NCI NIH HHS, Id: CA009138
  • Agency: NIGMS NIH HHS, Id: GM074917
  • Agency: NCRR NIH HHS, Id: P41 RR-01081
  • Agency: NIGMS NIH HHS, Id: R01 GM074917
  • Agency: NIGMS NIH HHS, Id: R01 GM074917-04
  • Agency: NCI NIH HHS, Id: T32 CA009138

Mesh Terms

  • Bone Neoplasms
  • DNA Damage
  • DNA Helicases
  • DNA Ligases
  • DNA Repair
  • DNA, Fungal
  • DNA-Binding Proteins
  • Gene Expression Regulation, Fungal
  • Humans
  • Lysine
  • Mutation
  • Osteosarcoma
  • Proliferating Cell Nuclear Antigen
  • S Phase
  • Saccharomyces cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Tumor Cells, Cultured
  • Ubiquitin
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligases
  • Ubiquitination