Suess, Beatrix (2005)
Engineered riboswitches control gene expression by small molecules.
In: Biochemical Society transactions, 33 (Pt 3)
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
We have developed conditional gene expression systems based on engineered small-molecule-binding riboswitches. Tetracycline-dependent regulation can be imposed on an mRNA in yeast by inserting an aptamer in its 5'-untranslated region. Biochemical and genetic analyses determined that binding of the ligand tetracycline leads to a pseudoknot-like linkage within the aptamer structure, thereby inhibiting the initial steps of translation. A second translational control element was designed by combining a theophylline aptamer with a communication module for which a 1 nt slipping mechanism had been proposed. This structural element was inserted close to the bacterial ribosomal binding site at a position just interfering with translation in the non-ligand-bound form. Addition of the ligand then shifts the inhibitory element to a distance that permits efficient translation.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2005 |
Autor(en): | Suess, Beatrix |
Art des Eintrags: | Bibliographie |
Titel: | Engineered riboswitches control gene expression by small molecules. |
Sprache: | Englisch |
Publikationsjahr: | 2005 |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Biochemical Society transactions |
Jahrgang/Volume einer Zeitschrift: | 33 |
(Heft-)Nummer: | Pt 3 |
Kurzbeschreibung (Abstract): | We have developed conditional gene expression systems based on engineered small-molecule-binding riboswitches. Tetracycline-dependent regulation can be imposed on an mRNA in yeast by inserting an aptamer in its 5'-untranslated region. Biochemical and genetic analyses determined that binding of the ligand tetracycline leads to a pseudoknot-like linkage within the aptamer structure, thereby inhibiting the initial steps of translation. A second translational control element was designed by combining a theophylline aptamer with a communication module for which a 1 nt slipping mechanism had been proposed. This structural element was inserted close to the bacterial ribosomal binding site at a position just interfering with translation in the non-ligand-bound form. Addition of the ligand then shifts the inhibitory element to a distance that permits efficient translation. |
Fachbereich(e)/-gebiet(e): | 10 Fachbereich Biologie > Synthetic Genetic Circuits (2020 umbenannt in "Synthetic RNA biology") 10 Fachbereich Biologie |
Hinterlegungsdatum: | 22 Feb 2012 11:07 |
Letzte Änderung: | 05 Mär 2013 09:59 |
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