Abstract
Ribozymes are ribonucleic acid (RNA) molecules capable of acting as enzymes even in the complete absence of proteins. They have the catalytic activity of breaking and/or forming covalent bonds with extraordinary specificity, accelerating the rate of these reactions. The ability of RNA to serve as a catalyst was first shown for the self-splicing group I intron of Tetrahymena and the RNA moiety of RNAse P (1–3). Subsequent to the discovery of these two RNA enzymes, RNA-mediated catalysis has been associated with the self-splicing group II introns of yeast, fungal, and plant mitochondria (as well as chloroplasts) (4); single-stranded plant viroid and virusoid RNAs (5–7); hepatitis delta virus (8); and a satellite RNA from Neurospora mitochondria (9). It is rather clear that the RNA component of the larger ribosomal subunit is functioning as a peptidyltransferase as well (10–13). The potential functioning of spliceosomal smaller nuclear (sn)RNAs as a ribozyme in complex with the premessenger RNA (pre-mRNA) to catalyze pre-mRNA splicing has also been proposed (14). It is highly likely that additional RNA catalytic motifs and new roles for RNA-mediated catalysis will also be found as more is learned about the genomes of a variety of organisms.
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Scherer, L., Rossi, J.J. (2005). Cancer Therapeutic Applications of Ribozymes and RNAi. In: Curiel, D.T., Douglas, J.T. (eds) Cancer Gene Therapy. Contemporary Cancer Research. Humana Press. https://doi.org/10.1007/978-1-59259-785-7_5
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