JCVI: Research / Projects / Synthetic Biology and the U.S. Biotechnology Regulatory System / Overview
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In recent years, a range of genetic engineering techniques referred to “synthetic biology” has significantly expanded the tool kit available to scientists and engineers, providing them with far greater capabilities to engineer organisms than previous techniques allowed. The field of synthetic biology includes the relatively new ability to synthesize long pieces of DNA from chemicals, as well as improved methods for genetic manipulation and design of genetic pathways to achieve more precise control of biological systems. These advances will help usher in a new generation of genetically engineered mi­crobes, plants, and animals.

The JCVI Policy Center Team, along with researchers at the University of Virginia and EMBO, examined how well the current U.S. regulatory system for genetically engineered products will handle the near-term introduction of organisms engineered using synthetic biology. In particular, the focus was on those organisms intended to be used or grown directly in the environment, outside of a contained facility.

The study concludes that the U.S. regulatory agen­cies have adequate legal authority to address most, but not all, potential environmental, health and safety con­cerns posed by these organisms. Such near-term products are likely to represent incremental changes rather than a marked departure from previous genetically engineered organisms. However, the study also identified two key challenges for the regulatory system, which are detailed in the report. First, USDA’s authority over genetically engineered plants depends on the use of an older engineering technique that is no longer necessary for many applications. The shift to synthetic biology and other newer genetic engineering techniques will leave many engineered plants without any premarket regulatory review. Second, the number and diversity of engineered microbes for commercial use will increase in the near future, challenging EPA’s resources, expertise, and perhaps authority to regulate them.


This report, funded by the Department of Energy with additional funds from the Alfred P. Sloan Foundation, is the result of a 2-year process that included interviews, discussions, and two workshops that sought input from a wide range of experts, including U.S. federal agency regulators, legal and science policy experts, representatives from the biotechnology indus­try, and non-governmental organiza­tions. This cross-section of views informed this report, but the conclusions are solely those of the authors.


Sarah Carter

Robert Friedman

Michael Rodemeyer

Michele Garfinkel