4.8 Article

Poly(ADP-ribose)-Dependent Regulation of DNA Repair by the Chromatin Remodeling Enzyme ALC1

Journal

SCIENCE
Volume 325, Issue 5945, Pages 1240-1243

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1177321

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Funding

  1. Wellcome Trust Senior Fellowship [064414]
  2. UK Biotechnology and Biological Sciences Research Council
  3. Medical Research Council (UK)
  4. European Union
  5. European Molecular Biology Organization
  6. Human Frontier Science Program Organization
  7. Louis-Jeantet Foundation

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Posttranslational modifications play key roles in regulating chromatin plasticity. Although various chromatin-remodeling enzymes have been described that respond to specific histone modifications, little is known about the role of poly[adenosine 5'-diphosphate (ADP)-ribose] in chromatin remodeling. Here, we identify a chromatin-remodeling enzyme, ALC1 (Amplified in Liver Cancer 1, also known as CHD1L), that interacts with poly(ADP-ribose) and catalyzes PARP1-stimulated nucleosome sliding. Our results define ALC1 as a DNA damage-response protein whose role in this process is sustained by its association with known DNA repair factors and its rapid poly(ADP-ribose)-dependent recruitment to DNA damage sites. Furthermore, we show that depletion or overexpression of ALC1 results in sensitivity to DNA-damaging agents. Collectively, these results provide new insights into the mechanisms by which poly(ADP-ribose) regulates DNA repair.

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