A CA+ Pair Adjacent to a Sheared GA or AA Pair Stabilizes Size-Symmetric RNA Internal Loops†

RNA internal loops are often important sites for folding and function. Residues in internal loops can have pKa values shifted close to neutral pH because of the local structural environment. A series of RNA internal loops were studied at different pH by UV absorbance versus temperature melting experiments and imino proton nuclear magnetic resonance (NMR). A stabilizing CA pair forms at pH 7 in the and nearest neighbors when the CA pair is the first noncanonical pair (loop-terminal pair) in 3 × 3 nucleotide and larger size-symmetric internal loops. These and nearest neighbors, with CA adjacent to a closing Watson−Crick pair, are further stabilized when the pH is lowered from 7 to 5.5. The results are consistent with a significantly larger fraction (from ∼20% at pH 7 to ∼90% at pH 5.5) of adenines being protonated at the N1 position to form stabilizing wobble CA+ pairs adjacent to a sheared GA or AA pair. The noncanonical pair adjacent to the GA pair in can either stabilize or destabilize the loop, consistent with the sequence-dependent thermodynamics of GA pairs. No significant pH-dependent stabilization is found for most of the other nearest neighbor combinations involving CA pairs (e.g., and ), which is consistent with the formation of various nonwobble pairs observed in different local sequence contexts in crystal and NMR structures. A revised free-energy model, including stabilization by wobble CA+ pairs, is derived for predicting stabilities of medium-size RNA internal loops.

[1]  Kristin Reiche,et al.  RNAstrand: reading direction of structured RNAs in multiple sequence alignments , 2007, Algorithms for Molecular Biology.

[2]  Emil Alexov,et al.  Calculation of pKas in RNA: on the structural origins and functional roles of protonated nucleotides. , 2007, Journal of molecular biology.

[3]  D. Turner,et al.  NMR structures of (rGCUGAGGCU)2 and (rGCGGAUGCU)2: probing the structural features that shape the thermodynamic stability of GA pairs. , 2007, Biochemistry.

[4]  R. Kierzek,et al.  A conformationally restricted guanosine analog reveals the catalytic relevance of three structures of an RNA enzyme. , 2007, Chemistry & biology.

[5]  M. Serra,et al.  Comprehensive thermodynamic analysis of 3′ double-nucleotide overhangs neighboring Watson–Crick terminal base pairs , 2006, Nucleic acids research.

[6]  Scott D Kennedy,et al.  An alternating sheared AA pair and elements of stability for a single sheared purine-purine pair flanked by sheared GA pairs in RNA. , 2006, Biochemistry.

[7]  D. Turner,et al.  Consecutive GA pairs stabilize medium-size RNA internal loops. , 2006, Biochemistry.

[8]  J. Holton,et al.  Structures of the Bacterial Ribosome at 3.5 Å Resolution , 2005, Science.

[9]  D. Turner,et al.  RNA challenges for computational chemists. , 2005, Biochemistry.

[10]  Linkage between proton binding and folding in RNA: implications for RNA catalysis. , 2005, Biochemical Society transactions.

[11]  D. Davis,et al.  Structural effects of hypermodified nucleosides in the Escherichia coli and human tRNALys anticodon loop: the effect of nucleosides s2U, mcm5U, mcm5s2U, mnm5s2U, t6A, and ms2t6A. , 2005, Biochemistry.

[12]  Yaroslava G. Yingling,et al.  Dynamic behavior of the telomerase RNA hairpin structure and its relationship to dyskeratosis congenita. , 2005, Journal of molecular biology.

[13]  Brent M. Znosko,et al.  Solution structure of an RNA internal loop with three consecutive sheared GA pairs. , 2005, Biochemistry.

[14]  Philip C Bevilacqua,et al.  Linkage between proton binding and folding in RNA: a thermodynamic framework and its experimental application for investigating pKa shifting. , 2005, RNA.

[15]  Brent M. Znosko,et al.  Structural features and thermodynamics of the J4/5 loop from the Candida albicans and Candida dubliniensis group I introns. , 2004, Biochemistry.

[16]  S. Butcher,et al.  Dynamics in the U6 RNA intramolecular stem-loop: a base flipping conformational change. , 2004, Biochemistry.

[17]  R. Andino,et al.  Solution structure of a consensus stem-loop D RNA domain that plays important roles in regulating translation and replication in enteroviruses and rhinoviruses. , 2004, Biochemistry.

[18]  Brent M. Znosko,et al.  Factors affecting thermodynamic stabilities of RNA 3 x 3 internal loops. , 2004, Biochemistry.

[19]  T. Dieckmann,et al.  The solution structure of the VS ribozyme active site loop reveals a dynamic "hot-spot". , 2004, Journal of molecular biology.

[20]  Scott A. Strobel,et al.  Crystal structure of a self-splicing group I intron with both exons , 2004, Nature.

[21]  S. Acharya,et al.  Significant pKa perturbation of nucleobases is an intrinsic property of the sequence context in DNA and RNA. , 2004, Journal of the American Chemical Society.

[22]  D. Turner,et al.  Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA secondary structure. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[23]  J. Wöhnert,et al.  The structure of the stemloop D subdomain of coxsackievirus B3 cloverleaf RNA and its interaction with the proteinase 3C. , 2004, Structure.

[24]  A. Ferré-D’Amaré The hairpin ribozyme. , 2004, Biopolymers.

[25]  Steven E. Brenner,et al.  SCOR: Structural Classification of RNA, version 2.0 , 2004, Nucleic Acids Res..

[26]  Joseph D Puglisi,et al.  Structure of HCV IRES domain II determined by NMR , 2003, Nature Structural Biology.

[27]  W. Olson,et al.  3DNA: a software package for the analysis, rebuilding and visualization of three-dimensional nucleic acid structures. , 2003, Nucleic acids research.

[28]  C. W. Hilbers,et al.  Structure of the pyrimidine-rich internal loop in the poliovirus 3'-UTR: the importance of maintaining pseudo-2-fold symmetry in RNA helices containing two adjacent non-canonical base-pairs. , 2003, Journal of molecular biology.

[29]  J. Wedekind,et al.  Crystal structure of the leadzyme at 1.8 A resolution: metal ion binding and the implications for catalytic mechanism and allo site ion regulation. , 2003, Biochemistry.

[30]  P. Bevilacqua Mechanistic considerations for general acid-base catalysis by RNA: revisiting the mechanism of the hairpin ribozyme. , 2003, Biochemistry.

[31]  C. Pleij,et al.  Protonation of non-Watson–Crick base pairs and encapsidation of turnip yellow mosaic virus RNA , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[32]  Eric Westhof,et al.  The non-Watson-Crick base pairs and their associated isostericity matrices. , 2002, Nucleic acids research.

[33]  Naoki Sugimoto,et al.  Long RNA dangling end has large energetic contribution to duplex stability. , 2002, Journal of the American Chemical Society.

[34]  Qin Zhao,et al.  NCIR: a database of non-canonical interactions in known RNA structures , 2002, Nucleic Acids Res..

[35]  J. Puglisi,et al.  RNAPack: an integrated NMR approach to RNA structure determination. , 2001, Methods.

[36]  S. Sato,et al.  Substrate recognition by ADAR1 and ADAR2. , 2001, RNA.

[37]  T. Dieckmann,et al.  A pH controlled conformational switch in the cleavage site of the VS ribozyme substrate RNA. , 2001, Journal of molecular biology.

[38]  J. Sühnel,et al.  Molecular Dynamics Simulation Reveals Conformational Switching of Water-Mediated Uracil-Cytosine Base Pairs in an RNA Duplex , 2022 .

[39]  H. Heus,et al.  Structure of the ribozyme substrate hairpin of Neurospora VS RNA: a close look at the cleavage site. , 2000, RNA.

[40]  J. Feigon,et al.  Adenine protonation in domain B of the hairpin ribozyme. , 2000, Biochemistry.

[41]  Oliver Weichenrieder,et al.  Structure and assembly of the Alu domain of the mammalian signal recognition particle , 2000, Nature.

[42]  C. Vonrhein,et al.  Structure of the 30S ribosomal subunit , 2000, Nature.

[43]  T. Steitz,et al.  The complete atomic structure of the large ribosomal subunit at 2.4 A resolution. , 2000, Science.

[44]  D. Turner,et al.  Factors affecting the thermodynamic stability of small asymmetric internal loops in RNA. , 2000, Biochemistry.

[45]  D. Turner,et al.  Nuclear magnetic resonance spectroscopy and molecular modeling reveal that different hydrogen bonding patterns are possible for G.U pairs: one hydrogen bond for each G.U pair in r(GGCGUGCC)(2) and two for each G.U pair in r(GAGUGCUC)(2). , 2000, Biochemistry.

[46]  D. Turner,et al.  Thermodynamics of single mismatches in RNA duplexes. , 1999, Biochemistry.

[47]  J. Sabina,et al.  Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. , 1999, Journal of molecular biology.

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

[49]  J. Sühnel,et al.  Quantum-Chemical Study of a Water-Mediated Uracil−Cytosine Base Pair , 1999 .

[50]  A. Pardi,et al.  NMR solution structure of the lead-dependent ribozyme: evidence for dynamics in RNA catalysis. , 1998, Journal of molecular biology.

[51]  Structure of a 16-mer RNA duplex r(GCAGACUUAAAUCUGC)2 with wobble C.A+ mismatches. , 1998, Journal of molecular biology.

[52]  D. Turner,et al.  Thermodynamic parameters for an expanded nearest-neighbor model for formation of RNA duplexes with Watson-Crick base pairs. , 1998, Biochemistry.

[53]  E. L. Holbrook,et al.  Structure of an RNA internal loop consisting of tandem C-A+ base pairs. , 1998, Biochemistry.

[54]  F. Major,et al.  Modeling active RNA structures using the intersection of conformational space: application to the lead-activated ribozyme. , 1998, RNA.

[55]  J. SantaLucia,et al.  Nearest-neighbor thermodynamics of internal A.C mismatches in DNA: sequence dependence and pH effects. , 1998, Biochemistry.

[56]  A. Pardi,et al.  A semiconserved residue inhibits complex formation by stabilizing interactions in the free state of a theophylline-binding RNA. , 1998, Biochemistry.

[57]  C. W. Hilbers,et al.  The detailed structure of tandem G.A mismatched base-pair motifs in RNA duplexes is context dependent. , 1997, Journal of molecular biology.

[58]  A. Pardi,et al.  Unusual dynamics and pKa shift at the active site of a lead dependent ribozyme , 1997 .

[59]  D. Turner,et al.  Investigation of the structural basis for thermodynamic stabilities of tandem GU mismatches: solution structure of (rGAGGUCUC)2 by two-dimensional NMR and simulated annealing. , 1996, Biochemistry.

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

[61]  S. Scaringe,et al.  Synthesis, deprotection, analysis and purification of RNA and ribozymes. , 1995, Nucleic acids research.

[62]  O Kennard,et al.  Structure of a mispaired RNA double helix at 1.6-A resolution and implications for the prediction of RNA secondary structure. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[63]  R. Thomas The denaturation of DNA. , 1993, Gene.

[64]  S. Smallcombe Solvent suppression with symmetrically-shifted pulses , 1993 .

[65]  I. Tinoco,et al.  Crystal structure of an RNA double helix incorporating a track of non-Watson–Crick base pairs , 1991, Nature.

[66]  I. Tinoco,et al.  Solution conformation of an RNA hairpin loop. , 1990, Biochemistry.

[67]  R. Cedergren,et al.  The automated chemical synthesis of long oligoribuncleotides using 2'-O-silylated ribonucleoside 3'-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3'-half molecule of an Escherichia coli formylmethionine tRNA , 1987 .

[68]  D. Turner,et al.  Base-stacking and base-pairing contributions to helix stability: thermodynamics of double-helix formation with CCGG, CCGGp, CCGGAp, ACCGGp, CCGGUp, and ACCGGUp. , 1983, Biochemistry.

[69]  M. Sundaralingam,et al.  Stacking of Crick Wobble pair and Watson-Crick pair: stability rules of G-U pairs at ends of helical stems in tRNAs and the relation to codon-anticodon Wobble interaction. , 1978, Nucleic acids research.

[70]  I. Tinoco,et al.  Stability of ribonucleic acid double-stranded helices. , 1974, Journal of molecular biology.

[71]  D. Crothers,et al.  Free energy of imperfect nucleic acid helices. 3. Small internal loops resulting from mismatches. , 1973, Journal of molecular biology.

[72]  M. Record Electrostatic effects on polynucleotide transitions. II. Behavior of titrated systems , 1967, Biopolymers.