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Cited by 187

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

The C-terminal domain of p53 recognizes DNA damaged by ionizing radiation.

Open access
Reed, M, Woelker, B, Wang, P, Wang, Y, Anderson, M E, Tegtmeyer, P·1995·Proceedings of the National Academy of Sciences

Abstract

p53 accumulates after DNA damage and arrests cellular growth. These findings suggest a possible role for p53 in the cellular response to DNA damage. We have previously shown that the C terminus of p53 binds DNA nonspecifically and assembles stable tetramers. In this study, we have utilized purified segments of human and murine p53s to determine which p53 domains may participate in a DNA damage response pathway. We find that the C-terminal 75 amino acids of human or murine p53 are necessary and sufficient for the DNA annealing and strand-transfer activities of p53. In addition, both full-length wild-type p53 and the C-terminal 75 amino acids display an increased binding affinity for DNA damaged by restriction digestion, DNase I treatment, or ionizing radiation. In contrast, the central site-specific DNA-binding domain together with the tetramerization domain does not have these activities. We propose that interactions of the C terminus of p53 with damaged DNA may play a role in the activation of p53 in response to DNA damage.

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Metadata

Authors
Reed, M., Woelker, B., Wang, P., Wang, Y., Anderson, M. E., & Tegtmeyer, P.
Venue
Proceedings of the National Academy of Sciences
Published
1995-10-10
Volume
92
Issue
21
Pages
9455-9459
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2006607764
Cited by
187
References
1
FWCI
8.25
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The C-terminal domain of p53 recognizes DNA damaged by ionizing radiation. https://app.cochat.ai/papers/10.1073/pnas.92.21.9455
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Reed, M., Woelker, B., Wang, P., Wang, Y., Anderson, M. E., & Tegtmeyer, P. (1995). The C-terminal domain of p53 recognizes DNA damaged by ionizing radiation. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.92.21.9455

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