Literature DB >> 10903205

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

E A Schultes1, D P Bartel.   

Abstract

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.

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Year:  2000        PMID: 10903205     DOI: 10.1126/science.289.5478.448

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  121 in total

1.  Design of multistable RNA molecules.

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5.  Perfectly complementary nucleic acid enzymes.

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6.  Using an RNA secondary structure partition function to determine confidence in base pairs predicted by free energy minimization.

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7.  The robustness of naturally and artificially selected nucleic acid secondary structures.

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Review 8.  The role of robustness in phenotypic adaptation and innovation.

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Journal:  Proc Biol Sci       Date:  2012-01-04       Impact factor: 5.349

9.  Structure and stability of RNA/RNA kissing complex: with application to HIV dimerization initiation signal.

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Journal:  RNA       Date:  2011-10-25       Impact factor: 4.942

10.  A domain-based model for predicting large and complex pseudoknotted structures.

Authors:  Song Cao; Shi-Jie Chen
Journal:  RNA Biol       Date:  2012-02-01       Impact factor: 4.652

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