A programming language for DNA

Artificial DNA-based circuits could someday program cellular behavior, authors say

| 2 min read

Register for free to listen to this article
Listen with Speechify
0:00
2:00
Share
Researchers have made an important leap in designing DNA-based circuits, reports this week's Science. They've created the first system that allows amplification of desired DNA sequences without using enzymes -- a step towards creating artificial biochemical circuits inside cells."They've begun to develop a programming language, a software, for DNA," said Andrew Ellington of the University of Texas at Austin. The work is "a significant advance over previous [attempts]," he added.Scientists have previously used DNA to build synthetic biochemical circuits. But these networks have generally only been designed to perform one task. "These were machines that carried out a particular function or solved a particular problem," Ellington told The Scientist. In the new work, "we show a method of designing them generally so that it can be applied basically to any sequence you want," said first author David Yu Zhang of the California Institute of Technology in Pasadena.Zhang and his colleagues created a network of reactions based on the base-pairing of six short, single-stranded DNA pieces. Domains on each DNA strand determine how the circuit components interact with each other.In each reaction, a DNA catalyst binds to a complementary DNA strand and displaces two other strands. Because this leads to increased disorder overall, the reaction is thermodynamically favorable. Unlike biological catalysis, the reaction requires no enzymes. Using this system, the authors achieved two types of signal amplification found in natural biological regulatory networks. They created a feedback amplification system, in which a reaction's product catalyzes its own reaction. According to the authors, such an autocatalytic system could eventually become an enzyme-free alternative to the polymerase chain reaction (PCR). They also created a chain of reactions that amplifies a desired final piece of DNA. "We can cascade these catalysts and have a serial amplification, kind of like a signal transduction system," Zhang said.Although they performed their work in DNA, the system should work equally well with RNA or synthetic nucleic acids, Zhang said. Ultimately, the goal of this type of research is to create independent networks that could operate in parallel to biological cellular networks, Zhang said. Such synthetic circuits could potentially detect aberrations in cellular functioning and respond by initiating "some therapeutic action that would be directed only to that cell," said John SantaLucia of Wayne State University in Detroit and DNA Software, Inc., in Ann Arbor, who wasn't involved in the work.The authors also showed that their circuits perform well in the presence of animal RNA and cell lysate--an important demonstration if such circuits are to be used inside cells, SantaLucia said. The system the researchers created is both simpler and more robust than any previous attempts, SantaLucia added. It may not be appropriate for technologies such as DNA-based computers that would require very complex computations, he said, but it would likely work well for "the kind of simple computations that you could do inside of a cell."Melissa Lee Phillips mail@the-scientist.comLinks within this article:"Engineering entropy-driven reactions and networks catalyzed by DNA," Science, November 16, 2007. http://www.sciencemag.orgJ. Lucentini, "Is this life?" The Scientist, January 1, 2006. http://www.the-scientist.com/article/display/18854/I. Oransky, "Molecular OS gets upgrade," The Scientist, October 11, 2004. http://www.the-scientist.com/article/display/14989/Andrew Ellington http://ellingtonlab.org/main/static.php?page=aboutusN.C. Seeman, "From genes to machines: DNA nanomechanical devices," Trends in Biochemical Sciences, March 2005. http://www.the-scientist.com/pubmed/15752983David Yu Zhang http://www.dna.caltech.edu/˜dzhang/W. Gloffke, "Quantitative PCR update," The Scientist, April 21, 2003. http://www.the-scientist.com/article/display/13720/S. Karkare, D. Bhatnagar, "Promising nucleic acid analogs and mimics: characteristic features and applications of PNA, LNA, and morpholino," Applied Microbiology and Biotechnology, August 2006. http://www.the-scientist.com/pubmed/16683135John SantaLucia http://ozone3.chem.wayne.edu/
Interested in reading more?

Become a Member of

The Scientist Logo
Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member? Login Here

Meet the Author

  • Melissa Lee Phillips

    This person does not yet have a bio.
Share
May digest 2025 cover
May 2025, Issue 1

Study Confirms Safety of Genetically Modified T Cells

A long-term study of nearly 800 patients demonstrated a strong safety profile for T cells engineered with viral vectors.

View this Issue
Detecting Residual Cell Line-Derived DNA with Droplet Digital PCR

Detecting Residual Cell Line-Derived DNA with Droplet Digital PCR

Bio-Rad
How technology makes PCR instruments easier to use.

Making Real-Time PCR More Straightforward

Thermo Fisher Logo
Characterizing Immune Memory to COVID-19 Vaccination

Characterizing Immune Memory to COVID-19 Vaccination

10X Genomics
Optimize PCR assays with true linear temperature gradients

Applied Biosystems™ VeriFlex™ System: True Temperature Control for PCR Protocols

Thermo Fisher Logo

Products

The Scientist Placeholder Image

Biotium Launches New Phalloidin Conjugates with Extended F-actin Staining Stability for Greater Imaging Flexibility

Leica Microsystems Logo

Latest AI software simplifies image analysis and speeds up insights for scientists

BioSkryb Genomics Logo

BioSkryb Genomics and Tecan introduce a single-cell multiomics workflow for sequencing-ready libraries in under ten hours

iStock

Agilent BioTek Cytation C10 Confocal Imaging Reader

agilent technologies logo