One sequence, two ribozymes: implications for the emergence of new ribozyme folds.

We describe a single RNA sequence that can assume either of two ribozyme folds and catalyze the two respective reactions. The two ribozyme folds share no evolutionary history and are completely different, with no base pairs (and probably no hydrogen bonds) in common. Minor variants of this sequence are highly active for one or the other reaction, and can be accessed from prototype ribozymes through a series of neutral mutations. Thus, in the course of evolution, new RNA folds could arise from preexisting folds, without the need to carry inactive intermediate sequences. This raises the possibility that biological RNAs having no structural or functional similarity might share a common ancestry. Furthermore, functional and structural divergence might, in some cases, precede rather than follow gene duplication.

[1]  John Maynard Smith,et al.  Natural Selection and the Concept of a Protein Space , 1970, Nature.

[2]  Dr. Susumu Ohno Evolution by Gene Duplication , 1970, Springer Berlin Heidelberg.

[3]  W R Engels,et al.  Gene duplication. , 1981, Science.

[4]  P. Schuster,et al.  From sequences to shapes and back: a case study in RNA secondary structures , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[5]  F. Lisacek,et al.  Automatic identification of group I intron cores in genomic DNA sequences. , 1994, Journal of molecular biology.

[6]  W. Hendrickson,et al.  Quantification of tertiary structural conservation despite primary sequence drift in the globin fold , 1994, Protein science : a publication of the Protein Society.

[7]  J W Szostak,et al.  Structurally complex and highly active RNA ligases derived from random RNA sequences. , 1995, Science.

[8]  D. Bartel,et al.  The secondary structure and sequence optimization of an RNA ligase ribozyme. , 1995, Nucleic acids research.

[9]  M. Huynen,et al.  Smoothness within ruggedness: the role of neutrality in adaptation. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J W Szostak,et al.  Nonenzymatic, template-directed ligation of oligoribonucleotides is highly regioselective for the formation of 3'-5' phosphodiester bonds. , 1996, Journal of the American Chemical Society.

[11]  J W Szostak,et al.  Kinetic and mechanistic analysis of nonenzymatic, template-directed oligoribonucleotide ligation. , 1996, Journal of the American Chemical Society.

[12]  T. Cech,et al.  Activity and thermostability of the small self-splicing group I intron in the pre-tRNA(lle) of the purple bacterium Azoarcus. , 1996, RNA.

[13]  P. S. Kim,et al.  Context-dependent secondary structure formation of a designed protein sequence , 1996, Nature.

[14]  P. Stadler,et al.  Neutral networks in protein space: a computational study based on knowledge-based potentials of mean force. , 1997, Folding & design.

[15]  S. Balasubramanian,et al.  Transmuting α helices and β sheets , 1997 .

[16]  P. Schuster,et al.  Generic properties of combinatory maps: neutral networks of RNA secondary structures. , 1997, Bulletin of mathematical biology.

[17]  G. S. Wickham,et al.  Self-cleaving ribozymes of hepatitis delta virus RNA. , 1997, European journal of biochemistry.

[18]  A. Ferré-D’Amaré,et al.  Crystal structure of a hepatitis delta virus ribozyme , 1998, Nature.

[19]  A. T. Perrotta,et al.  A toggle duplex in hepatitis delta virus self-cleaving RNA that stabilizes an inactive and a salt-dependent pro-active ribozyme conformation. , 1998, Journal of molecular biology.

[20]  P. Schuster,et al.  IR-98-039 / April Continuity in Evolution : On the Nature of Transitions , 1998 .

[21]  W. Krzyzosiak,et al.  Patterns of cleavages induced by lead ions in defined RNA secondary structure motifs. , 1998, Journal of molecular biology.

[22]  D. Patel,et al.  RNA architecture dictates the conformations of a bound peptide. , 1999, Chemistry & biology.

[23]  Ronald R. Breaker,et al.  Kinetics of RNA Degradation by Specific Base Catalysis of Transesterification Involving the 2‘-Hydroxyl Group , 1999 .

[24]  R. Sauer,et al.  Evolution of a protein fold in vitro. , 1999, Science.

[25]  F E Cohen,et al.  Protein misfolding and prion diseases. , 1999, Journal of molecular biology.

[26]  P. Schuster,et al.  RNA folding at elementary step resolution. , 1999, RNA.