1. Academic Validation
  2. The RNA helicase Aquarius exhibits structural adaptations mediating its recruitment to spliceosomes

The RNA helicase Aquarius exhibits structural adaptations mediating its recruitment to spliceosomes

  • Nat Struct Mol Biol. 2015 Feb;22(2):138-44. doi: 10.1038/nsmb.2951.
Inessa De 1 Sergey Bessonov 2 Romina Hofele 3 Karine dos Santos 4 Cindy L Will 2 Henning Urlaub 5 Reinhard Lührmann 2 Vladimir Pena 1
Affiliations

Affiliations

  • 1 Macromolecular Crystallography, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  • 2 Department of Cellular Biochemistry, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  • 3 Bioanalytical Mass Spectrometry, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  • 4 Department of Structural Biochemistry, Free University, Berlin, Germany.
  • 5 1] Bioanalytical Mass Spectrometry, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany. [2] Bioanalytics, Department of Clinical Chemistry, University Medical Center, Göttingen, Germany.
Abstract

Aquarius is a multifunctional putative RNA helicase that binds precursor-mRNA introns at a defined position. Here we report the crystal structure of human Aquarius, revealing a central RNA helicase core and several unique accessory domains, including an ARM-repeat domain. We show that Aquarius is integrated into spliceosomes as part of a pentameric intron-binding complex (IBC) that, together with the ARM domain, cross-links to U2 snRNP proteins within activated spliceosomes; this suggests that the latter aid in positioning Aquarius on the intron. Aquarius's ARM domain is essential for IBC formation, thus indicating that it has a key protein-protein-scaffolding role. Finally, we provide evidence that Aquarius is required for efficient precursor-mRNA splicing in vitro. Our findings highlight the remarkable structural adaptations of a helicase to achieve position-specific recruitment to a ribonucleoprotein complex and reveal a new building block of the human spliceosome.

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