Roquin binding to target mRNAs involves a winged helix-turn-helix motif

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作者
Anja Schuetz
Yasuhiro Murakawa
Eva Rosenbaum
Markus Landthaler
Udo Heinemann
机构
[1] Helmholtz Protein Sample Production Facility,
[2] Max Delbrück Center for Molecular Medicine,undefined
[3] Laboratory for RNA Biology and Posttranscriptional Regulation,undefined
[4] Berlin Institute for Medical Systems Biology,undefined
[5] Max Delbrück Center for Molecular Medicine,undefined
[6] Structure and Membrane Interaction of G-Proteins,undefined
[7] Max Delbrück Center for Molecular Medicine,undefined
[8] Chemistry and Biochemistry Institute,undefined
[9] Freie Universität Berlin,undefined
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Roquin proteins mediate mRNA deadenylation by recognizing a conserved class of stem-loop RNA degradation motifs via their Roquin domain. Here we present the crystal structure of a Roquin domain, revealing a mostly helical protein fold bearing a winged helix-turn-helix motif. By combining structural, biochemical and mutation analyses, we gain insight into the mode of RNA binding. We show that the winged helix-turn-helix motif is involved in the binding of constitutive decay elements-containing stem-loop mRNAs. Moreover, we provide biochemical evidence that Roquin proteins are additionally able to bind to duplex RNA and have the potential to be functional in different oligomeric states.
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