4.8 Article

Preferential binding of ATR protein to UV-damaged DNA

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NATL ACAD SCIENCES
DOI: 10.1073/pnas.102167799

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Funding

  1. NCI NIH HHS [P30 CA016086, CA16086] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM031819, GM31819, R01 GM032833, GM32833] Funding Source: Medline

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The ATR protein is a member of the phosphoinositide 3-kinase-related kinase family and plays an important role in UV-induced DNA damage checkpoint response. Its role as a signal transducer in cell cycle checkpoint is well established, but it is currently unclear whether ATR functions as a damage sensor as well. Here we have purified the ATR protein and investigated its interaction with DNA by using biochemical analysis and electron microscopy. We find that ATR is a DNA-binding protein with higher affinity to UV-damaged than undamaged DNA. In addition, damaged DNA stimulates the kinase activity of ATR to a significantly higher level than undamaged DNA. Our data suggest that ATR may function as an initial sensor in the DNA damage checkpoint response.

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