Skip Navigation
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Your Environment. Your Health.

Publication Detail

Title: Proliferating cell nuclear antigen prevents trinucleotide repeat expansions by promoting repeat deletion and hairpin removal.

Authors: Beaver, Jill M; Lai, Yanhao; Rolle, Shantell J; Liu, Yuan

Published In DNA Repair (Amst), (2016 12)

Abstract: DNA base lesions and base excision repair (BER) within trinucleotide repeat (TNR) tracts modulate repeat instability through the coordination among the key BER enzymes DNA polymerase β, flap endonuclease 1 (FEN1) and DNA ligase I (LIG I). However, it remains unknown whether BER cofactors can also alter TNR stability. In this study, we discovered that proliferating cell nuclear antigen (PCNA), a cofactor of BER, promoted CAG repeat deletion and removal of a CAG repeat hairpin during BER in a duplex CAG repeat tract and CAG hairpin loop, respectively. We showed that PCNA stimulated LIG I activity on a nick across a small template loop during BER in a duplex (CAG)20 repeat tract promoting small repeat deletions. Surprisingly, we found that during BER in a hairpin loop, PCNA promoted reannealing of the upstream flap of a double-flap intermediate, thereby facilitating the formation of a downstream flap and stimulating FEN1 cleavage activity and hairpin removal. Our results indicate that PCNA plays a critical role in preventing CAG repeat expansions by modulating the structures of dynamic DNA via cooperation with BER enzymes. We provide the first evidence that PCNA prevents CAG repeat expansions during BER by promoting CAG repeat deletion and removal of a TNR hairpin.

PubMed ID: 27793507 Exiting the NIEHS site

MeSH Terms: Base Sequence*; DNA Damage; DNA Ligase ATP/genetics*; DNA Ligase ATP/metabolism; DNA Polymerase beta/genetics*; DNA Polymerase beta/metabolism; DNA Repair; DNA-(Apurinic or Apyrimidinic Site) Lyase/genetics; DNA-(Apurinic or Apyrimidinic Site) Lyase/metabolism; Flap Endonucleases/genetics*; Flap Endonucleases/metabolism; Gene Expression; Humans; Nucleic Acid Conformation; Proliferating Cell Nuclear Antigen/genetics*; Proliferating Cell Nuclear Antigen/metabolism; Sequence Deletion*; Trinucleotide Repeat Expansion*; Trinucleotide Repeats

Back
to Top