The modular genetic circuits engineered from parts of otherwise unrelated bacterial genomes can be set up to handle multiple chemical inputs simultaneously with a minimum of interference from their neighbours. The work reported in the American Chemical Society journal ACS Synthetic Biology gives scientists more options as they design synthetic cells for specific tasks, such as the production of biofuels, environmental remediation or the treatment of human diseases. The researchers are creating complex genetic logic circuits similar to those used to build traditional computers and electrical devices. In a simple circuit, if one input and another input are both present, the circuit carries out its instruction. With genetic circuitry based on this type of Boolean logic, a genetic logic circuit might prompt the creation of a specific protein when it senses two chemicals — or prompt a cell’s DNA to repress the creation of that protein. Simple circuits have become easier to create as synthetic biologists develop more tools, but they require more sophisticated tools for complex problems. Rice’s Matthew Bennett and his colleagues are intent upon following a path similar to that of computer programmers whose capabilities grew from simple Pong to the immersive worlds of modern games. “One of the ultimate goals of this technology is to allow cells to sense and respond to their environment in programmatic ways,” said Bennett, an assistant professor of biochemistry and cell biology. “We want to be able to program cells to go into an environment and do what they’re supposed to do. Right now, one of the main ways we do that is through transcriptional logic gates. These are akin to electronic circuits — the logic gates in our computers. In cells, they work a little bit differently, but there are a lot of parallels.” Logic gates designed by Bennett’s team and others react in a programmed way when they sense chemicals in their immediate environment. If certain combinations of chemicals are present in the environment, the gate will turn on a gene that may either repress or promote the expression of a protein. “A lot of work in synthetic biology has gone into programming cells to make decisions better and more efficiently,” Bennett said. “That’s what this paper is addressing. We found a new way of creating very modular and easy-to-use genetic systems to create highly responsive transcriptional logic.” The research led by Rice graduate student David Shis drew from a genetic toolbox of chimeric (with parts from different sources) transcription factors. These modular proteins incorporate the gene regulatory capacity of one transcription factor and the environmental sensing capabilities of another. The researchers demonstrated that as many as four chimeras with the same DNA-binding modules can work together and serve as gates with multiple inputs, either repressing — or overriding the repression of — specific genes. They successfully tested the ability of chimera combinations in the bacteria Escherichia coli to up- or down-regulate the expression of a gene encoding green fluorescent protein. “Often, when you make a genetic logic gate, you have to have many genes in the background to allow the gate to work,” Bennett said. “We’ve been able to eliminate the need for that by programming transcription factors — which are specific proteins that turn genes on and off — to respond to their environment directly and activate a specific gene in a very modular way. We can now program both environmental sensing and downstream genetic regulation into the same module,” he said. Bennett said he sees synthetic biology addressing many issues. “We might be able to use cells to report on, or remediate, environmental pollution. Or we might be able to program them to find a tumor in your body and respond to it. Metabolic engineers might find complex synthetic circuits that are able to adjust on the fly, he said. “In fermentation, for example, you might want gene regulation in the cells to change as a process evolves. These new circuits can sense different sugars in the culture and direct gene regulation to maximize production.” Co-authors include Rice alumna Faiza Hussain and Sarah Meinhardt and Liskin Swint-Kruse, both of the University of Kansas Medical Center. Swint-Kruse, an associate professor of biochemistry and molecular biology at KUMC, is a former postdoctoral researcher and research scientist at Rice. The National Institutes of Health, through the joint National Science Foundation/National Institute of General Medical Sciences Mathematical Biology Program, and the Robert A. Welch Foundation supported the research.
Original publication:
David L. Shis, Faiza Hussain, Sarah Meinhardt, Liskin Swint-Kruse, Matthew R. Bennett. Modular, Multi-Input Transcriptional Logic Gating with Orthogonal LacI/GalR Family Chimeras.ACS Synthetic Biology, 2014; 140728104557004DOI: 10.1021/sb500262f Source: Rice University
