Processivity of ribozyme-catalyzed RNA polymerization.

The "RNA world" hypothesis proposes that early in the evolution of life, before the appearance of DNA or protein, RNA was responsible both for encoding genetic information and for catalyzing biochemical reactions. Ribo-organisms living in the RNA world would have replicated their RNA genomes by using an RNA polymerase ribozyme. Efforts to provide experimental support for the RNA world hypothesis have focused on producing such a polymerase, and in vitro evolution methods have led to the isolation of a polymerase ribozyme that catalyzes primer extension which is accurate and general, but slow. To understand the reaction of this ribozyme, we developed a method of measuring polymerase processivity that is particularly useful in the case of an inefficient polymerase. This method allowed us to demonstrate that the polymerase ribozyme, despite its inefficiency, is partially processive. It is currently limited by a low affinity for the primer-template duplex, but once it successfully binds the primer-template duplex in the productive alignment, it catalyzes an extension reaction that is so rapid that it can occur multiple times during the short span of a single binding event. This finding contributes to the understanding of one of the more sophisticated activities yet to be generated de novo in the laboratory and sheds light on the parameters to be targeted for further optimization.

[1]  Terry L. Marsh,et al.  Rna catalysis and the origin of life , 2005, Origins of life and evolution of the biosphere.

[2]  W. McClure,et al.  The kinetics and processivity of nucleic acid polymerases. , 1980, Methods in enzymology.

[3]  L. Orgel Evolution of the genetic apparatus. , 1968, Journal of molecular biology.

[4]  I. Lehman,et al.  On the processive mechanism of Escherichia coli DNA polymerase I. , 1975, The Journal of biological chemistry.

[5]  John Kuriyan,et al.  Three-dimensional structure of the β subunit of E. coli DNA polymerase III holoenzyme: A sliding DNA clamp , 1992, Cell.

[6]  S. H. Wilson,et al.  Studies on the mechanism of Escherichia coli DNA polymerase I large fragment. Chain termination and modulation by polynucleotides. , 1982, The Journal of biological chemistry.

[7]  R. Bambara,et al.  Size classes of products synthesized processively by DNA polymerase III and DNA polymerase III holoenzyme of Escherichia coli. , 1981, The Journal of biological chemistry.

[8]  M. Eigen Selforganization of matter and the evolution of biological macromolecules , 1971, Naturwissenschaften.

[9]  H. Echols,et al.  Fidelity mechanisms in DNA replication. , 1991, Annual review of biochemistry.

[10]  B. Ganem RNA world , 1987, Nature.

[11]  Robert E. Johnson,et al.  Fidelity and Processivity of Saccharomyces cerevisiae DNA Polymerase η* , 1999, The Journal of Biological Chemistry.

[12]  N. Bergman,et al.  Metal ion requirements for structure and catalysis of an RNA ligase ribozyme. , 2002, Biochemistry.

[13]  S. H. Wilson,et al.  Studies on the mechanism of DNA polymerase alpha. Nascent chain elongation, steady state kinetics, and the initiation phase of DNA synthesis. , 1981, The Journal of biological chemistry.

[14]  T. Kunkel Biological asymmetries and the fidelity of eukaryotic DNA replication , 1992, BioEssays : news and reviews in molecular, cellular and developmental biology.

[15]  David P. Bartel,et al.  5 Re-creating an RNA Replicase , 1999 .

[16]  L E Orgel,et al.  RNA catalysis and the origins of life. , 1986, Journal of theoretical biology.

[17]  D. Bartel,et al.  RNA-Catalyzed RNA Polymerization: Accurate and General RNA-Templated Primer Extension , 2001, Science.