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Effect of Rap1 binding on DNA distortion and potassium permanganate hypersensitivity.

TitleEffect of Rap1 binding on DNA distortion and potassium permanganate hypersensitivity.
Publication TypeJournal Article
Year of Publication2013
AuthorsLe Bihan, Y-V, Matot, B, Pietrement, O, Giraud-Panis, M-J, Gasparini, S, Le Cam, E, Gilson, E, Sclavi, B, Miron, S, Le Du, M-H
JournalActa Crystallogr D Biol Crystallogr
Volume69
IssuePt 3
Pagination409-19
Date Published2013 Mar
ISSN1399-0047
KeywordsArginine, Crystallography, X-Ray, Cytosine, DNA, Fungal, Hydrogen Bonding, Nucleic Acid Conformation, Potassium Permanganate, Protein Binding, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Solutions, Telomere-Binding Proteins, Transcription Factors
Abstract

Repressor activator protein 1 (Rap1) is an essential factor involved in transcription and telomere stability in the budding yeast Saccharomyces cerevisiae. Its interaction with DNA causes hypersensitivity to potassium permanganate, suggesting local DNA melting and/or distortion. In this study, various Rap1-DNA crystal forms were obtained using specifically designed crystal screens. Analysis of the DNA conformation showed that its distortion was not sufficient to explain the permanganate reactivity. However, anomalous data collected at the Mn edge using a Rap1-DNA crystal soaked in potassium permanganate solution indicated that the DNA conformation in the crystal was compatible with interaction with permanganate ions. Sequence-conservation analysis revealed that double-Myb-containing Rap1 proteins all carry a fully conserved Arg580 at a position that may favour interaction with permanganate ions, although it is not involved in the hypersensitive cytosine distortion. Permanganate reactivity assays with wild-type Rap1 and the Rap1[R580A] mutant demonstrated that Arg580 is essential for hypersensitivity. AFM experiments showed that wild-type Rap1 and the Rap1[R580A] mutant interact with DNA over 16 successive binding sites, leading to local DNA stiffening but not to accumulation of the observed local distortion. Therefore, Rap1 may cause permanganate hypersensitivity of DNA by forming a pocket between the reactive cytosine and Arg580, driving the permanganate ion towards the C5-C6 bond of the cytosine.

DOI10.1107/S0907444912049311
Alternate JournalActa Crystallogr. D Biol. Crystallogr.
PubMed ID23519416