Comparative analysis of hairpin ribozyme structures and interference data.

Great strides in understanding the molecular underpinnings of RNA catalysis have been achieved with advances in RNA structure determination by NMR spectroscopy and X-ray crystallography. Despite these successes the functional relevance of a given structure can only be assessed upon comparison with biochemical studies performed on functioning RNA molecules. The hairpin ribozyme presents an excellent case study for such a comparison. The active site is comprised of two stems each with an internal loop that forms a series of non-canonical base pairs. These loops dock into each other to create an active site for catalysis. Recently, three independent structures have been determined for this catalytic RNA, including two NMR structures of the isolated loop A and loop B stems and a high-resolution crystal structure of both loops in a docked conformation. These structures differ significantly both in their tertiary fold and the nature of the non-canonical base pairs formed within each loop. Several of the chemical groups required to achieve a functioning hairpin ribozyme have been determined by nucleotide analog interference mapping (NAIM). Here we compare the three hairpin structures with previously published NAIM data to assess the convergence between the structural and functional data. While there is significant disparity between the interference data and the individual NMR loop structures, there is almost complete congruity with the X-ray structure. The only significant differences cluster around an occluded pocket adjacent to the scissile phosphate. These local differences may suggest a role for these atoms in the transition state, either directly in chemistry or via a local structural rearrangement.

[1]  S. Strobel,et al.  Investigation of adenosine base ionization in the hairpin ribozyme by nucleotide analog interference mapping. , 2001, RNA.

[2]  A. Ferré-D’Amaré,et al.  Crystal structure of a hairpin ribozyme–inhibitor complex with implications for catalysis , 2001, Nature.

[3]  John M. Burke,et al.  A conformational change in the "loop E-like" motif of the hairpin ribozyme is coincidental with domain docking and is essential for catalysis. , 2001, Biochemistry.

[4]  J. Doudna,et al.  Ribozyme structures and mechanisms. , 2000, Annual review of biochemistry.

[5]  F. Major,et al.  Structural basis for the guanosine requirement of the hairpin ribozyme. , 1999, Biochemistry.

[6]  S. Strobel,et al.  Nucleotide analog interference mapping of the hairpin ribozyme: implications for secondary and tertiary structure formation. , 1999, Journal of molecular biology.

[7]  K. J. Young,et al.  The role of essential pyrimidines in the hairpin ribozyme-catalysed reaction. , 1999, Journal of molecular biology.

[8]  Frédéric H.-T. Allain,et al.  Solution structure of the loop B domain from the hairpin ribozyme , 1999, Nature Structural Biology.

[9]  S. Strobel,et al.  A minor groove RNA triple helix within the catalytic core of a group I intron , 1998, Nature Structural Biology.

[10]  S. Strobel,et al.  Ribozyme chemogenetics. , 1998, Biopolymers.

[11]  S. Strobel,et al.  Complementary sets of noncanonical base pairs mediate RNA helix packing in the group I intron active site , 1998, Nature Structural Biology.

[12]  E. Westhof,et al.  Inter-domain cross-linking and molecular modelling of the hairpin ribozyme. , 1997, Journal of molecular biology.

[13]  N. Walter,et al.  Real-time monitoring of hairpin ribozyme kinetics through base-specific quenching of fluorescein-labeled substrates. , 1997, RNA.

[14]  I. Tinoco,et al.  Solution structure of loop A from the hairpin ribozyme from tobacco ringspot virus satellite. , 1996, Biochemistry.

[15]  U. Sørensen,et al.  Base and sugar requirements for RNA cleavage of essential nucleoside residues in internal loop B of the hairpin ribozyme: implications for secondary structure. , 1996, Nucleic acids research.

[16]  J. Grasby,et al.  Purine functional groups in essential residues of the hairpin ribozyme required for catalytic cleavage of RNA. , 1995, Biochemistry.

[17]  S. Butcher,et al.  Structure-mapping of the hairpin ribozyme. Magnesium-dependent folding and evidence for tertiary interactions within the ribozyme-substrate complex. , 1994, Journal of molecular biology.

[18]  J. Grasby,et al.  Synthetic oligoribonucleotides carrying site-specific modifications for RNA structure-function analysis. , 1994, Biochimie.

[19]  John M. Burke,et al.  Four ribose 2'-hydroxyl groups essential for catalytic function of the hairpin ribozyme. , 1993, The Journal of biological chemistry.

[20]  S. Butcher,et al.  Essential nucleotide sequences and secondary structure elements of the hairpin ribozyme. , 1993, The EMBO journal.

[21]  John M. Burke,et al.  Novel guanosine requirement for catalysis by the hairpin ribozyme , 1991, Nature.

[22]  John M. Burke,et al.  Binding and cleavage of nucleic acids by the "hairpin" ribozyme. , 1991, Biochemistry.

[23]  W. Gerlach,et al.  Sequences required for self-catalysed cleavage of the satellite RNA of tobacco ringspot virus. , 1989, Gene.

[24]  R. Tritz,et al.  RNA catalytic properties of the minimum (-)sTRSV sequence. , 1989, Biochemistry.

[25]  W. Gerlach,et al.  Sequences required for self-catalysed cleavage of the satellite RNA of tobacco ringspot virus**Presented at the Albany Conference on ‘RNA: Catalysis, Splicing, Evolution’, Rensselaerville, NY (U.S.A.) 22-25 September, 1988. , 1989 .

[26]  J. M. Buzayan,et al.  Nucleic Acids Research Nucleotide sequence and newly formed phosphodJester bond of spontaneously Ugated satellite tobacco ringspot virus RNA , 2005 .