Synthetic Sensors

Engineered circuits detect endogenous transcription factors to drive cellular outputs.

By | December 1, 2016

SYNTHETIC CIRCUIT: In this example of a typical transducer, the genetic construct (top) includes an amplifier response element and a carefully positioned transcription factor response element upstream of a promoter that drives expression of a fusion gene (the combined effector of choice and an amplifier). In the presence of a specific endogenous transcription factor, which binds to the transcription factor response element, the fusion gene is expressed. Cleavage of the fusion protein releases the amplifier, which together with the transcription factor drives much stronger expression. The system is like a positive feedback loop, but neither the transcription factor nor the amplifier alone can drive strong expression—they need each other.

Some synthetic biology applications use cells as mere hosts for engineered genetic circuits—for example, when cells act as factories for desired molecules. For other applications, however, researchers would like to integrate the synthetic circuits with the cell’s own pathways.

Such integrated systems could be used to sense particular molecules and induce appropriate responses. For instance, detection of a metastasis-inducing protein in a cancer cell might be used to trigger that cell’s suicide. “The concept is that these synthetic circuits will be able to read out bits and pieces of information from the cell and interpret them to make decisions and drive the cell in different directions,” says Yaakov “Kobi” Benenson of the Federal Institute of Technology, or ETH, in Zurich.

Benenson and colleagues have recently generated genetic constructs—or “transducers”—that can detect the presence of specific transcription factors in human cells and, in response, activate synthetic processes—such as the expression of particular proteins, the silencing of mRNAs (via microRNA production), or the induction of targeted genetic recombination.

The constructs are similar to tissue-specific expression vectors, in which promoters with cell type–specific activity are used to drive transcription of a desired gene or genes. The difference, however, is in the constructs’ precision design and ability to detect cell states, not just cell types, says Benenson.

Having established key design principles, the team was able to create transducers that detect a variety of different transcription factors. In one scenario, for example, detection of the developmental transcription factor Sox10 drove Cre recombinase activity and, in turn, the recombination-dependent expression of a fluorescent reporter.

The nice thing, says biological engineer Ron Weiss of MIT, is that “in principle, [the constructs] are relatively modular so you can plug-and-play” with the particular factor you want to detect. (Cell Rep, 16:2525-37, 2016)

Cell-specific expression vectors DNA sequence contains a cell-type specific promoter and the gene, or genes, of interest. Low. Promoter region may bind many transcription factors. Expressing a gene of interest in a desired cell type, e.g., production of a fluorescent protein for observation of a specific tissue under a microscope
Transcription factor–
specific transducers
DNA sequence contains one or more carefully designed transcription factor response elements, a minimal promoter, an amplifier system, and the gene, or genes, of interest. High. These constructs are designed to detect one, or a combination of, specific transcription factors. Inducing a particular designed activity in response to
the presence of one or more specific transcription factors.
Unlike cell-specific promoters, these constructs can
be turned on during discrete cell states, including transient conditions.


Add a Comment

Avatar of: You



Sign In with your LabX Media Group Passport to leave a comment

Not a member? Register Now!

LabX Media Group Passport Logo

Popular Now

  1. So You’ve Been Mistaken as a White Nationalist
  2. Opinion: We Need a Replacement for Beall’s List
  3. Trump Releases Science Spending Priorities for FY2019
  4. Seeding the Gut Microbiome Prevents Sepsis in Infants