Identification in a pseudoknot of a U⋅G motif essential for the regulation of the expression of ribosomal protein S15
Open Access
- 3 March 1998
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 95 (5) , 2564-2567
- https://doi.org/10.1073/pnas.95.5.2564
Abstract
The ribosomal protein S15 from Escherichia coli binds to a pseudoknot in its own messenger. This interaction is an essential step in the mechanism of S15 translational autoregulation. In a previous study, a recognition determinant for S15 autoregulation, involving a U⋅G wobble pair, was located in the center of stem I of the pseudoknot. In this study, an extensive mutagenesis analysis has been conducted in and around this U⋅G pair by comparing the effects of these mutations on the expression level of S15. The results show that the U⋅G wobble pair cannot be substituted by A⋅G, C⋅A, A⋅C, G⋅U, or C⋅G without loss of the autocontrol. In addition, the base pair C⋅G, adjacent to the 5′ side of U, cannot be flipped or changed to another complementary base pair without also inducing derepression of translation. A unique motif, made of only two adjacent base pairs, U⋅G/C⋅G, is essential for S15 autoregulation and is presumably involved in direct recognition by the S15 protein.Keywords
This publication has 34 references indexed in Scilit:
- Functional Evidence for Indirect Recognition of G·U in tRNA Ala by Alanyl-tRNA SynthetaseScience, 1996
- Structure of the P1 Helix from Group I Self-splicing IntronsJournal of Molecular Biology, 1995
- Mutational analysis of the pseudoknot structure of the S15 translational operator from Escherichia coliMolecular Microbiology, 1994
- Translational Repression by the Bacteriophage T4 Gene 32 Protein Involves Specific Recognition of an RNA Pseudoknot StructureJournal of Molecular Biology, 1993
- Functional contacts of a transfer RNA synthetase with 2′-hydroxyl groups in the RNA minor grooveNature, 1992
- NMR analysis of helix I from the 5S RNA of Escherichia coliBiochemistry, 1992
- Crystal structure of an RNA double helix incorporating a track of non-Watson–Crick base pairsNature, 1991
- Target site of Escherichia coli ribosomal protein S15 on its messenger RNAJournal of Molecular Biology, 1990
- Translational autocontrol of the Escherichia coli ribosomal protein S15Journal of Molecular Biology, 1990
- A simple structural feature is a major determinant of the identity of a transfer RNANature, 1988