The RNA Ligase ribozyme was the first of several types of synthetic ribozymes produced by in vitro evolution and selection techniques. They are an important class of ribozymes because they catalyze the assembly of RNA fragments into phosphodiester RNA polymers, a reaction required of all extant nucleic acid polymerases and thought to be required for any self-replicating molecule. Ideas that the origin of life may have involved the first self-replicating molecules being ribozymes are called RNA World hypotheses. Ligase ribozymes may have been part of such a pre-biotic RNA world.
In order to copy RNA, fragments or monomers (individual building blocks) that have 5′-triphosphates must be ligated together. This is true for modern (protein-based) polymerases, and is also the most likely mechanism by which a ribozyme self-replicase in an RNA world might function. Yet no one has found a natural ribozyme that can perform this reaction.
In vitro evolution and selection edit
RNA in vitro evolution or SELEX enables the artificial evolution and selection of RNA molecules that possess a desired property, such as binding affinity for a particular ligand or an activity such as that of an enzyme or catalyst. The first such selections involved isolation of various aptamers that bind to small molecules. The first catalytic RNAs produced by in vitro evolution were RNA ligases, catalytic RNAs that join two RNA fragments to produce a single adduct. The most active ligase known to date is the Class I ligase, isolated from random sequence (work of David Bartel, while in the Szostak lab). Other examples of RNA ligases include the L1 ligase (Robertson and Ellington), the R3C ligase (Joyce), the DSL ligase (Inoue). All these ligases catalyze the formation of a 3′–5′ phosphodiester bond between two RNA fragments.
The L1 ligase edit
Michael Robertson and Andrew Ellington evolved a ligase ribozyme that performs the desired 5′–3′ RNA assembly reaction, and called this the L1 ligase.[1] To better understand the details of how this ribozyme folds into a structure that permits it to catalyze this fundamental reaction, the X-ray crystal structure has been solved.[2][3] The structure is composed of three helical stems called stem A, B and C, that connect at a three helix junction.
References edit
- ^ Robertson MP, Hesselberth JR, Ellington AD (April 2001). "Optimization and optimality of a short ribozyme ligase that joins non-Watson-Crick base pairings". RNA. 7 (4): 513–523. doi:10.1017/S1355838201002199. PMC 1370105. PMID 11345430.
- ^ Robertson MP, Scott WG (March 2007). "The structural basis of ribozyme-catalyzed RNA assembly". Science. 315 (5818): 1549–1553. Bibcode:2007Sci...315.1549R. doi:10.1126/science.1136231. PMID 17363667. S2CID 11530091.
- ^ Joyce GF (March 2007). "Structural biology. A glimpse of biology's first enzyme". Science. 315 (5818): 1507–1508. doi:10.1126/science.1140736. PMID 17363651. S2CID 82057900.
Further reading edit
- Giambasu GM, Lee TS, Sosa CP, Robertson MP, Scott WG, York DM (April 2010). "Identification of dynamical hinge points of the L1 ligase molecular switch". RNA. 16 (4): 769–780. doi:10.1261/rna.1897810. PMC 2844624. PMID 20167653.
- Pitt JN, Ferré-D'Amaré AR (March 2009). "Structure-guided engineering of the regioselectivity of RNA ligase ribozymes". J. Am. Chem. Soc. 131 (10): 3532–3540. doi:10.1021/ja8067325. PMC 2678027. PMID 19220054.
- Robertson MP, Knudsen SM, Ellington AD (January 2004). "In vitro selection of ribozymes dependent on peptides for activity". RNA. 10 (1): 114–127. doi:10.1261/rna.5900204. PMC 1370523. PMID 14681590.
- Robertson MP, Ellington AD (April 2000). "Design and optimization of effector-activated ribozyme ligases". Nucleic Acids Res. 28 (8): 1751–1759. doi:10.1093/nar/28.8.1751. PMC 102822. PMID 10734194.