TY - JOUR
T1 - Rational Re-engineering of a Transcriptional Silencing PreQ1 Riboswitch.
AU - Wu, Ming-Cheng
AU - Lowe, Phillip
AU - Robinson, Christopher
AU - Vincent, Helen
AU - Dixon, Neil
AU - Leigh, James
AU - Micklefield, Jason
PY - 2015/6/24
Y1 - 2015/6/24
N2 - Re-engineered riboswitches that no longer respond to cellular metabolites, but which instead can be controlled by synthetic molecules, are potentially useful gene regulatory tools for use in synthetic biology and biotechnology fields. Previously, extensive genetic selection and screening approaches were employed to re-engineer a natural adenine riboswitch to create orthogonal ON-switches, enabling translational control of target gene expression in response to synthetic ligands. Here we describe how a rational targeted approach was used to re-engineer the PreQ1 riboswitch from Bacillus subtilis into an orthogonal OFF-switch. In this case, the evaluation of just six synthetic compounds with seven riboswitch mutants, led to the identification of an orthogonal riboswitch-ligand pairing which effectively repressed the transcription of selected genes in B. subtilis. The streamlining of the re-engineering approach, and its extension to a second class of riboswitches, provides a methodological platform for the creation of new orthogonal regulatory components for biotechnological applications including gene functional analysis, antimicrobial target validation and screening.
AB - Re-engineered riboswitches that no longer respond to cellular metabolites, but which instead can be controlled by synthetic molecules, are potentially useful gene regulatory tools for use in synthetic biology and biotechnology fields. Previously, extensive genetic selection and screening approaches were employed to re-engineer a natural adenine riboswitch to create orthogonal ON-switches, enabling translational control of target gene expression in response to synthetic ligands. Here we describe how a rational targeted approach was used to re-engineer the PreQ1 riboswitch from Bacillus subtilis into an orthogonal OFF-switch. In this case, the evaluation of just six synthetic compounds with seven riboswitch mutants, led to the identification of an orthogonal riboswitch-ligand pairing which effectively repressed the transcription of selected genes in B. subtilis. The streamlining of the re-engineering approach, and its extension to a second class of riboswitches, provides a methodological platform for the creation of new orthogonal regulatory components for biotechnological applications including gene functional analysis, antimicrobial target validation and screening.
U2 - 10.1021/jacs.5b03405
DO - 10.1021/jacs.5b03405
M3 - Article
C2 - 26106809
SN - 0002-7863
VL - 137
SP - 9015
EP - 9021
JO - J. Am. Chem. Soc.
JF - J. Am. Chem. Soc.
ER -