Melting and chemical modification of a cyclized self-splicing group I intron: similarity of structures in 1 M Na+, in 10 mM Mg2+, and in the presence of substrate.

C IVS is the cyclized form of the intron from the RNA precursor of the Tetrahymena thermophila large subunit (LSU) ribosomal RNA. C IVS was mapped by chemical modification in 1 M Na+, 0.05 M Na+ and 10 mM Mg2+ (Na+/Mg2+), and Na+/Mg2+ with CUCU substrate. The results suggest the secondary structure is similar for all three conditions. Optical melting curves were also measured for C IVS in 1 M Na+ and Na+/Mg2+ and indicate the secondary structures have similar stabilities under both conditions. Computer predictions of secondary structure and stability are in good agreement with observations. The results suggest that many of the approximations used for computer prediction of secondary structure by free energy minimization are reasonable.

[1]  Daniel Herschlag,et al.  DNA cleavage catalysed by the ribozyme from Tetrahymena , 1990, Nature.

[2]  Jan van Duin,et al.  Control of prokaryotic translational initiation by mRNA secondary structure , 1990 .

[3]  D. Turner,et al.  Predicting optimal and suboptimal secondary structure for RNA. , 1990, Methods in enzymology.

[4]  D. Turner,et al.  Binding of a Fluorescent Oligonucleotide to a Circularized Intervening Sequence from Tetrahymena thermophila , 1989 .

[5]  O. Uhlenbeck,et al.  Studies on the hammerhead RNA self-cleaving domain. , 1989, Gene.

[6]  G. F. Joyce,et al.  Catalytic activity is retained in the Tetrahymena group I intron despite removal of the large extension of element P5. , 1989, Nucleic acids research.

[7]  D. Turner,et al.  Improved predictions of secondary structures for RNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[8]  K. Danenberg,et al.  Characterization of the mode of binding of substrates to the active site of Tetrahymena self-splicing RNA using 5-fluorouracil-substituted mini-exons. , 1989, Biochemistry.

[9]  T. Cech,et al.  Defining the inside and outside of a catalytic RNA molecule. , 1989, Science.

[10]  T. Cech,et al.  Stereochemistry of RNA cleavage by the Tetrahymena ribozyme and evidence that the chemical step is not rate-limiting. , 1989, Science.

[11]  M. Zuker On finding all suboptimal foldings of an RNA molecule. , 1989, Science.

[12]  D. Turner,et al.  Effects of substrate structure on the kinetics of circle opening reactions of the self-splicing intervening sequence from Tetrahymena thermophila: evidence for substrate and Mg2+ binding interactions. , 1989, Nucleic acids research.

[13]  T. Cech,et al.  Conserved sequences and structures of group I introns: building an active site for RNA catalysis--a review. , 1988, Gene.

[14]  J. Burke Molecular genetics of group I introns: RNA structures and protein factors required for splicing--a review. , 1988, Gene.

[15]  T. Cech,et al.  Sequence-specific endoribonuclease activity of the Tetrahymena ribozyme: enhanced cleavage of certain oligonucleotide substrates that form mismatched ribozyme-substrate complexes. , 1988, Biochemistry.

[16]  H. Noller,et al.  Model for the three-dimensional folding of 16 S ribosomal RNA. , 1988, Journal of molecular biology.

[17]  D. Turner,et al.  Kinetics for reaction of a circularized intervening sequence with CU, UCU, CUCU, and CUCUCU: mechanistic implications from the dependence on temperature and on oligomer and Mg2+ concentrations. , 1988, Biochemistry.

[18]  T. Cech,et al.  Deletion of nonconserved helices near the 3' end of the rRNA intron of Tetrahymena thermophila alters self-splicing but not core catalytic activity. , 1988, Genes & development.

[19]  Richard A. Coliins Evidence of natural selection to maintain a functional domain outside of the 'core' in a large subclass of group I introns. , 1988 .

[20]  I. Tinoco,et al.  A pseudoknotted RNA oligonucleotide , 1988, Nature.

[21]  R. Brimacombe,et al.  A detailed model of the three-dimensional structure of Escherichia coli 16 S ribosomal RNA in situ in the 30 S subunit. , 1988, Journal of molecular biology.

[22]  D. Turner,et al.  RNA structure prediction. , 1988, Annual review of biophysics and biophysical chemistry.

[23]  H. Noller,et al.  Structural analysis of RNA using chemical and enzymatic probing monitored by primer extension. , 1988, Methods in enzymology.

[24]  Sung-Hou Kim,et al.  Three-dimensional model of the active site of the self-splicing rRNA precursor of Tetrahymena. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Ebel,et al.  Probing the structure of RNAs in solution. , 1987, Nucleic acids research.

[26]  H. Tabak,et al.  Structural conventions for group I introns. , 1987, Nucleic acids research.

[27]  T. Cech,et al.  Selection of circularization sites in a group I IVS RNA requires multiple alignments of an internal template-like sequence , 1987, Cell.

[28]  K. Breslauer,et al.  Calculating thermodynamic data for transitions of any molecularity from equilibrium melting curves , 1987, Biopolymers.

[29]  D. Turner,et al.  Sequence dependence for the energetics of dangling ends and terminal base pairs in ribonucleic acid. , 1987, Biochemistry.

[30]  D. Turner,et al.  Sequence dependence for the energetics of terminal mismatches in ribooligonucleotides. , 1987, Biochemistry.

[31]  D. Turner,et al.  Free energy increments for hydrogen bonds in nucleic acid base pairs , 1987 .

[32]  D M Crothers,et al.  Proton nuclear magnetic resonance studies on bulge-containing DNA oligonucleotides from a mutational hot-spot sequence. , 1987, Biochemistry.

[33]  J. Sturtevant Biochemical Applications of Differential Scanning Calorimetry , 1987 .

[34]  C. E. Longfellow,et al.  Polymer-supported RNA synthesis and its application to test the nearest-neighbor model for duplex stability. , 1986, Biochemistry.

[35]  D. Turner,et al.  Improved free-energy parameters for predictions of RNA duplex stability. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[36]  J. Szostak Enzymatic activity of the conserved core of a group I self-splicing intron , 1986, Nature.

[37]  H. Blöcker,et al.  Predicting DNA duplex stability from the base sequence. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[38]  S. Altman,et al.  M1 RNA, the RNA subunit of Escherichia coli ribonuclease P, can undergo a pH-sensitive conformational change. , 1986, Biochemistry.

[39]  H. Noller,et al.  Rapid chemical probing of conformation in 16 S ribosomal RNA and 30 S ribosomal subunits using primer extension. , 1986, Journal of molecular biology.

[40]  T. Cech,et al.  The intervening sequence RNA of Tetrahymena is an enzyme. , 1986, Science.

[41]  T. Cech,et al.  Reversibility of cyclization of the tetrahymena rRNA intervening sequence: implication for the mechanism of splice site choice , 1985, Cell.

[42]  D. Turner,et al.  Contributions of dangling end stacking and terminal base-pair formation to the stabilities of XGGCCp, XCCGGp, XGGCCYp, and XCCGGYp helixes. , 1985, Biochemistry.

[43]  C. Pleij,et al.  A new principle of RNA folding based on pseudoknotting. , 1985, Nucleic acids research.

[44]  R. Waring,et al.  The tetrahymena rRNA intron self-splices in E. coli: In vivo evidence for the importance of key base-paired regions of RNA for RNA enzyme function , 1985, Cell.

[45]  T. Cech,et al.  Secondary structure of the circular form of the Tetrahymena rRNA intervening sequence: a technique for RNA structure analysis using chemical probes and reverse transcriptase. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[46]  R. Dickerson,et al.  Reverse-phase polystyrene column for purification and analysis of DNA oligomers. , 1984, Analytical Chemistry.

[47]  R. Waring,et al.  Assessment of a model for intron RNA secondary structure relevant to RNA self-splicing--a review. , 1984, Gene.

[48]  M. Caruthers,et al.  In situ activation of bis-dialkylaminophosphines--a new method for synthesizing deoxyoligonucleotides on polymer supports. , 1984, Nucleic acids research.

[49]  R. Lavery,et al.  A new theoretical index of biochemical reactivity combining steric and electrostatic factors. An application to yeast tRNAPhe. , 1984, Biophysical chemistry.

[50]  R. Zagursky,et al.  Expression of the phage λ recombination genes exo and bet under lacPO control on a multi-copy plasmid , 1983 .

[51]  R. Waring,et al.  Close relationship between certain nuclear and mitochondrial introns. Implications for the mechanism of RNA splicing. , 1983, Journal of molecular biology.

[52]  M. Zuker,et al.  Secondary structure of the Tetrahymena ribosomal RNA intervening sequence: structural homology with fungal mitochondrial intervening sequences. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[53]  T. Cech,et al.  Autocatalytic cyclization of an excised intervening sequence RNA is a cleavage–ligation reaction , 1983, Nature.

[54]  B. Dujon,et al.  Conservation of RNA secondary structures in two intron families including mitochondrial‐, chloroplast‐ and nuclear‐encoded members. , 1983, The EMBO journal.

[55]  R. Waring,et al.  Making ends meet: a model for RNA splicing in fungal mitochondria , 1982, Nature.

[56]  T. Cech,et al.  Self-splicing RNA: Autoexcision and autocyclization of the ribosomal RNA intervening sequence of tetrahymena , 1982, Cell.

[57]  C. Pleij,et al.  The tRNA-like structure at the 3' terminus of turnip yellow mosaic virus RNA. Differences and similarities with canonical tRNA. , 1982, Nucleic acids research.

[58]  M. Caruthers,et al.  Synthesis of deoxyoligonucleotides on a polymer support , 1981 .

[59]  Michael Zuker,et al.  Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information , 1981, Nucleic Acids Res..

[60]  M. Caruthers,et al.  Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis , 1981 .

[61]  D. Riesner,et al.  Structure and structure formation of viroids. , 1979, Journal of molecular biology.

[62]  D. Peattie,et al.  Direct chemical method for sequencing RNA. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[63]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[64]  W. Gilbert,et al.  A new method for sequencing DNA. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[65]  D. Crothers,et al.  The molecular mechanism of thermal unfolding of Escherichia coli formylmethionine transfer RNA. , 1974, Journal of molecular biology.

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

[67]  N. Leonard,et al.  Reaction of diethyl pyrocarbonate with nucleic acid components. Bases and nucleosides derived from guanine, cytosine, and uracil. , 1973, Journal of the American Chemical Society.

[68]  D. Crothers,et al.  Conformational changes of transfer ribonucleic acid. Equilibrium phase diagrams. , 1972, Biochemistry.

[69]  I. Tinoco,et al.  Estimation of Secondary Structure in Ribonucleic Acids , 1971, Nature.

[70]  M. Levitt Detailed Molecular Model for Transfer Ribonucleic Acid , 1969, Nature.

[71]  M. Litt Structural studies on transfer ribonucleic acid. I. Labeling of exposed guanine sites in yeast phenylalanine transfer ribonucleic acid with kethoxal. , 1969, Biochemistry.

[72]  Homer Jacobson,et al.  Intramolecular Reaction in Polycondensations. I. The Theory of Linear Systems , 1950 .