Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex

John McGeehan, Neil J. Ball, Simon Streeter, Sarah Thresh, Geoff Kneale

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The controller protein C.Esp1396I regulates the timing of gene expression of the restriction–modification (RM) genes of the RM system Esp1396I. The molecular recognition of promoter sequences by such transcriptional regulators is poorly understood, in part because the DNA sequence motifs do not conform to a well-defined symmetry. We report here the crystal structure of the controller protein bound to a DNA operator site. The structure reveals how two different symmetries within the operator are simultaneously recognized by the homo-dimeric protein, underpinned by a conformational change in one of the protein subunits. The recognition of two different DNA symmetries through movement of a flexible loop in one of the protein subunits may represent a general mechanism for the recognition of pseudo-symmetric DNA sequences.
    Original languageEnglish
    Pages (from-to)4158-4167
    Number of pages10
    JournalNucleic Acids Research
    Volume40
    Issue number9
    DOIs
    Publication statusPublished - 30 Dec 2012

    Fingerprint

    Dive into the research topics of 'Recognition of dual symmetry by the controller protein C.Esp1396I based on the structure of the transcriptional activation complex'. Together they form a unique fingerprint.

    Cite this