The solution structure of DNA-free Pax-8 paired box domain accounts for redox regulation of transcriptional activity in the Pax protein family

Luca Codutti, Hugo Van Ingen, Carlo Vascotto, Federico Fogolari, Alessandra Corazza, Gianluca Tell, Franco Quadrifoglio, Paolo Viglino, Rolf Boelens, Gennaro Esposito

    Research output: Contribution to journalArticle

    Abstract

    Pax-8 is a transcription factor belonging to the PAX genes superfamily and its crucial role has been proven both in embryo and in the adult organism. Pax-8 activity is regulated via a redox-based mechanism centered on the glutathionylation of specific cysteines in the N-terminal region (Cys 45 and Cys57). These residues belong to a highly evolutionary conserved DNA binding site: the Paired Box (Prd) domain. Crystallographic protein-DNA complexes of the homologues Pax-6 and Pax-5 showed a bipartite Prd domain consisting of two helix-turn-helix (HTH) motifs separated by an extended linker region. Here, by means of nuclear magnetic resonance, we show for the first time that the HTH motifs are largely defined in the unbound Pax-8 Prd domain. Our findings contrast with previous induced fit models, in which Pax-8 is supposed to largely fold upon DNA binding. Importantly, our data provide the structural basis for the enhanced chemical reactivity of residues Cys45 and Cys57 and explain clinical missense mutations that are not obviously related to the DNA binding interface of the paired box domain. Finally, sequence conservation suggests that our findings could be a general feature of the Pax family transcription factors.

    Original languageEnglish (US)
    Pages (from-to)33321-33328
    Number of pages8
    JournalJournal of Biological Chemistry
    Volume283
    Issue number48
    DOIs
    StatePublished - Nov 28 2008

    Fingerprint

    Oxidation-Reduction
    Helix-Turn-Helix Motifs
    DNA
    Paired Box Transcription Factors
    Proteins
    Transcription Factors
    Chemical reactivity
    Missense Mutation
    Cysteine
    Conservation
    Magnetic Resonance Spectroscopy
    Embryonic Structures
    Genes
    Binding Sites
    Nuclear magnetic resonance

    ASJC Scopus subject areas

    • Biochemistry
    • Cell Biology
    • Molecular Biology

    Cite this

    The solution structure of DNA-free Pax-8 paired box domain accounts for redox regulation of transcriptional activity in the Pax protein family. / Codutti, Luca; Van Ingen, Hugo; Vascotto, Carlo; Fogolari, Federico; Corazza, Alessandra; Tell, Gianluca; Quadrifoglio, Franco; Viglino, Paolo; Boelens, Rolf; Esposito, Gennaro.

    In: Journal of Biological Chemistry, Vol. 283, No. 48, 28.11.2008, p. 33321-33328.

    Research output: Contribution to journalArticle

    Codutti, L, Van Ingen, H, Vascotto, C, Fogolari, F, Corazza, A, Tell, G, Quadrifoglio, F, Viglino, P, Boelens, R & Esposito, G 2008, 'The solution structure of DNA-free Pax-8 paired box domain accounts for redox regulation of transcriptional activity in the Pax protein family', Journal of Biological Chemistry, vol. 283, no. 48, pp. 33321-33328. https://doi.org/10.1074/jbc.M805717200
    Codutti, Luca ; Van Ingen, Hugo ; Vascotto, Carlo ; Fogolari, Federico ; Corazza, Alessandra ; Tell, Gianluca ; Quadrifoglio, Franco ; Viglino, Paolo ; Boelens, Rolf ; Esposito, Gennaro. / The solution structure of DNA-free Pax-8 paired box domain accounts for redox regulation of transcriptional activity in the Pax protein family. In: Journal of Biological Chemistry. 2008 ; Vol. 283, No. 48. pp. 33321-33328.
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