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Related Concept Videos

Reporter Genes02:11

Reporter Genes

Reporter genes are a type of protein-coding gene that are often tagged to a gene of interest. Once inside a target cell, reporter genes usually produce visually identifiable characteristics like fluorescence and luminescence when expressed along with the gene of interest. Thus, reporter genes “report” the presence or absence of genes of interest in an organism, determine the gene expression pattern, or track the physical location of a DNA segment or protein in the cell.
Commonly used reporter...

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Updated: Jun 27, 2026

Rapid Optimization of a Light-Inducible System to Control Mammalian Gene Expression
09:08

Rapid Optimization of a Light-Inducible System to Control Mammalian Gene Expression

Published on: November 4, 2025

Design and Implementation of a Blue-Light-Controlled Gene-Switch System.

Chen Li1, Yuan Shi1, Xinyan Jiang1

  • 1Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest A&F University, Yangling 712100, China.

Molecules (Basel, Switzerland)
|June 26, 2026
PubMed
Summary
This summary is machine-generated.

We engineered a novel synthetic biology system for precise gene control using blue light and a chemical off-switch. This programmable tool enhances biomanufacturing, antimicrobial therapy, and environmental applications.

Keywords:
T7 RNA polymerasebenzoic acidoptogeneticssynthetic biology

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Area of Science:

  • Synthetic Biology
  • Genetic Engineering
  • Molecular Biology

Background:

  • Synthetic biology aims to create predictable and programmable biological systems.
  • Precise spatiotemporal gene control is crucial for applications like biomanufacturing, therapy, and microbial engineering.

Purpose of the Study:

  • To develop a blue-light-inducible T7 RNA polymerase (T7RNAP) system with dual-input regulation for precise gene control.
  • To optimize the system for enhanced expression, fidelity, and responsiveness.

Main Methods:

  • Optimization involved modifying ribosome binding site (RBS) sequences and evaluating split-T7RNAP variants.
  • Tandem T7 promoters were tested to balance gene expression yield and fidelity.
  • Bactericidal efficacy and expression levels were measured using fluorescent output and real-time growth curves under blue light.

Main Results:

  • RBS variants led to significant expression differences (up to 50-fold).
  • Three tandem T7 promoters offered optimal yield and fidelity.
  • A benzoate-responsive module achieved 4.5-fold repression, demonstrating effective chemical "off-switching" without hindering light induction.

Conclusions:

  • The developed system integrates precise blue light control with environmental responsiveness for on-demand gene activation.
  • The benzoate-triggered off-switch is valuable for biocontainment and bioremediation, enabling gene expression shutdown in response to pollutants.
  • Its modular and orthogonal design facilitates context-dependent control for diverse applications including biosensors, probiotics, and antimicrobial delivery systems.