4.5 Article

Structural and biochemical basis for misfolded RNA recognition by the Ro autoantigen

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 13, Issue 11, Pages 1002-1009

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb1156

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Funding

  1. NIGMS NIH HHS [R01-GM073863, R01 GM070521, R01 GM073863-03, R01 GM073863-01, R01 GM073863-02, R01 GM073863-04, R01 GM073863, R01-GM70521] Funding Source: Medline

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The Ro autoantigen is ring-shaped, binds misfolded noncoding RNAs and is proposed to function in quality control. Here we determine how Ro interacts with misfolded RNAs. Binding of Ro to misfolded precursor (pre)-5S ribosomal RNA requires a single-stranded 3' end and helical elements. As mutating most sequences of the helices and tail results in modest decreases in binding, Ro may be able to associate with a range of RNAs. Ro binds several other RNAs that contain single-stranded tails. A crystal structure of Ro bound to a misfolded pre-5S rRNA fragment reveals that the tail inserts into the cavity, while a helix binds on the surface. Most contacts of Ro with the helix are to the backbone. Mutagenesis reveals that Ro has an extensive RNA-binding surface. We propose that Ro uses this surface to scavenge RNAs that fail to bind their specific RNA-binding proteins.

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