P53 C-terminal interaction with DNA ends and gaps has opposing effect on specific DNA binding by the core

Sergey B. Zotchev, Marina Protopopova, Galina Selivanova

Publications: Contribution to journalArticlePeer Reviewed

Abstract

In addition to binding DNA in a sequence-specific manner, the p53 tumour suppressor protein can interact with damaged DNA. In order to understand which structural features in DNA the C-terminal domain recognises we have studied the interaction of p53 protein with different types of DNA oligonucleotides imitating damaged DNA. Here we show that one unpaired nucleotide within double-stranded (ds)DNA is sufficient for recognition by the p53 C-terminus, either as a protruding end or as an internal gap in dsDNA. C-terminal interaction with DNA ends facilitated core domain binding to DNA, whereas interaction with gaps prevented core domain-DNA complexing, implying that p53 might adopt distinct conformations upon binding to different DNA lesions. These observations suggest that both single-strand and double-strand breaks can serve as a target for p53 C-terminal recognition in vivo and indicate that p53 might recruit different repair factors to the sites of damaged DNA depending on the type of lesion.

Original languageEnglish
Pages (from-to)4005-4012
Number of pages8
JournalNucleic Acids Research
Volume28
Issue number20
Publication statusPublished - 15 Oct 2000
Externally publishedYes

Austrian Fields of Science 2012

  • 106022 Microbiology

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