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A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage.

UV-sensitive syndrome (UV(S)S) is a recently-identified autosomal recessive disorder characterized by mild cutaneous symptoms and defective transcription-coupled repair (TC-NER), the subpathway of nucleotide excision repair (NER) that rapidly removes damage that can block progression of the transcription machinery in actively-transcribed regions of DNA. Cockayne syndrome (CS) is another genetic disorder with sun sensitivity and defective TC-NER, caused by mutations in the CSA or CSB genes. The clinical hallmarks of CS include neurological/developmental abnormalities and premature aging. UV(S)S is genetically heterogeneous, in that it appears in individuals with mutations in CSB or in a still-unidentified gene. We report the identification of a UV(S)S patient (UV(S)S1VI) with a novel mutation in the CSA gene (p.trp361cys) that confers hypersensitivity to UV light, but not to inducers of oxidative damage that are notably cytotoxic in cells from CS patients. The defect in UV(S)S1VI cells is corrected by expression of the WT CSA gene. Expression of the p.trp361cys-mutated CSA cDNA increases the resistance of cells from a CS-A patient to oxidative stress, but does not correct their UV hypersensitivity. These findings imply that some mutations in the CSA gene may interfere with the TC-NER-dependent removal of UV-induced damage without affecting its role in the oxidative stress response. The differential sensitivity toward oxidative stress might explain the difference between the range and severity of symptoms in CS and the mild manifestations in UV(s)S patients that are limited to skin photosensitivity without precocious aging or neurodegeneration.

Pubmed ID: 19329487


  • Nardo T
  • Oneda R
  • Spivak G
  • Vaz B
  • Mortier L
  • Thomas P
  • Orioli D
  • Laugel V
  • Stary A
  • Hanawalt PC
  • Sarasin A
  • Stefanini M


Proceedings of the National Academy of Sciences of the United States of America

Publication Data

April 14, 2009

Associated Grants

  • Agency: NCI NIH HHS, Id: CA91456

Mesh Terms

  • Adolescent
  • Cells, Cultured
  • Child
  • Cockayne Syndrome
  • DNA Damage
  • DNA Repair Enzymes
  • Female
  • Humans
  • Infant
  • Mutation
  • Oxidation-Reduction
  • Oxidative Stress
  • Sensitivity and Specificity
  • Transcription Factors
  • Transcription, Genetic
  • Ultraviolet Rays