4.8 Article

Accurate placement of substrate RNA by Gar1 in H/ACA RNA-guided pseudouridylation

Journal

NUCLEIC ACIDS RESEARCH
Volume 43, Issue 15, Pages 7207-7216

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkv757

Keywords

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Funding

  1. National Key Basic Research Foundation of China [2010CB912302, 2012CB917304]
  2. National Natural Science Foundation of China [21233002, 91027044, 21373016]

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H/ACA RNA-guided ribonucleoprotein particle (RNP), the most complicated RNA pseudouridylase so far known, uses H/ACA guide RNA for substrate capture and four proteins (Cbf5, Nop10, L7Ae and Gar1) for pseudouridylation. Although it was shown that Gar1 not only facilitates the product release, but also enhances the catalytic activity, the chemical role that Gar1 plays in this complicated machinery is largely unknown. Kinetics measurement on Pyrococcus furiosus RNPs at different temperatures making use of fluorescence anisotropy showed that Gar1 reduces the catalytic barrier through affecting the activation entropy instead of enthalpy. Site-directed mutagenesis combined with molecular dynamics simulations demonstrated that V149 in the thumb loop of Cbf5 is critical in placing the target uridine to the right position toward catalytic D85 of Cbf5. The enzyme elegantly aligns the position of uridine in the catalytic site with the help of Gar1. In addition, conversion of uridine to pseudouridine results in a rigid syn configuration of the target nucleotide in the active site and causes Gar1 to pull out the thumb. Both factors guarantee the efficient release of the product.

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