Literature DB >> 17466623

Solution structure of an rRNA substrate bound to the pseudouridylation pocket of a box H/ACA snoRNA.

Hong Jin1, J Patrick Loria, Peter B Moore.   

Abstract

Base pairing between the RNA components of box H/ACA small nucleolar ribonucleoproteins (snoRNPs) and sequences in other eukaryotic RNAs target specific uridines for pseudouridylation. An RNA called HJ1 has been developed that interacts with the rRNA sequence targeted by the 5' pseudouridylation pocket of human U65 snoRNA the same way as intact U65 snoRNA. Sequences on both strands of the analog of the U65 snoRNP pseudouridylation pocket in HJ1 pair with its substrate sequence, and the resulting complex, called HJ3, is strongly stabilized by Mg(2+). The solution structure of HJ3 reveals an Omega-shaped RNA interaction motif that has not previously been described, which is likely to be common to all box H/ACA snoRNP-substrate complexes. The topology of the complex explains why the access of substrate sequences to snoRNPs is facile and how uridine selection may occur when these complexes form.

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Year:  2007        PMID: 17466623     DOI: 10.1016/j.molcel.2007.03.014

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  26 in total

Review 1.  Unveiling substrate RNA binding to H/ACA RNPs: one side fits all.

Authors:  Hong Li
Journal:  Curr Opin Struct Biol       Date:  2008-02       Impact factor: 6.809

2.  Long-distance placement of substrate RNA by H/ACA proteins.

Authors:  Bo Liang; Elliot J Kahen; Kate Calvin; Jing Zhou; Mario Blanco; Hong Li
Journal:  RNA       Date:  2008-08-28       Impact factor: 4.942

Review 3.  The box H/ACA ribonucleoprotein complex: interplay of RNA and protein structures in post-transcriptional RNA modification.

Authors:  Tomoko Hamma; Adrian R Ferré-D'Amaré
Journal:  J Biol Chem       Date:  2009-11-16       Impact factor: 5.157

4.  Mutational analysis of a viral RNA element that counteracts rapid RNA decay by interaction with the polyadenylate tail.

Authors:  Nicholas K Conrad; Mei-Di Shu; Katherine E Uyhazi; Joan A Steitz
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-11       Impact factor: 11.205

5.  Structure of H/ACA RNP protein Nhp2p reveals cis/trans isomerization of a conserved proline at the RNA and Nop10 binding interface.

Authors:  Bon-Kyung Koo; Chin-Ju Park; Cesar F Fernandez; Nicholas Chim; Yi Ding; Guillaume Chanfreau; Juli Feigon
Journal:  J Mol Biol       Date:  2011-06-25       Impact factor: 5.469

6.  The H/ACA RNP assembly factor SHQ1 functions as an RNA mimic.

Authors:  Hélène Walbott; Rosario Machado-Pinilla; Dominique Liger; Magali Blaud; Stéphane Réty; Petar N Grozdanov; Kate Godin; Herman van Tilbeurgh; Gabriele Varani; U Thomas Meier; Nicolas Leulliot
Journal:  Genes Dev       Date:  2011-11-15       Impact factor: 11.361

Review 7.  Structures of ribonucleoprotein particle modification enzymes.

Authors:  Bo Liang; Hong Li
Journal:  Q Rev Biophys       Date:  2010-11-26       Impact factor: 5.318

Review 8.  RNA pseudouridylation: new insights into an old modification.

Authors:  Junhui Ge; Yi-Tao Yu
Journal:  Trends Biochem Sci       Date:  2013-02-04       Impact factor: 13.807

9.  Structure of a functional ribonucleoprotein pseudouridine synthase bound to a substrate RNA.

Authors:  Bo Liang; Jing Zhou; Elliot Kahen; Rebecca M Terns; Michael P Terns; Hong Li
Journal:  Nat Struct Mol Biol       Date:  2009-05-28       Impact factor: 15.369

10.  Structure and functional studies of the CS domain of the essential H/ACA ribonucleoparticle assembly protein SHQ1.

Authors:  Mahavir Singh; Fernando A Gonzales; Duilio Cascio; Nathanael Heckmann; Guillaume Chanfreau; Juli Feigon
Journal:  J Biol Chem       Date:  2008-11-19       Impact factor: 5.157

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