Gene Expression: From On-Off Switch to Dial

Fine-tuning metabolic gene expression helps identify variants in yeast genes.

Gradient of the betaxanthins production in yeast across various different cultures. (Courtesy of Matthew Deaner)

The Science

Scientists have developed a more nuanced library approach to tuning gene expression in metabolic pathways. Compared to the traditional way, which leverages an all-or-nothing approach to expression, scientists can now opt for various shades of grey. The ability to fine-tune the level of gene expression allowed researchers to identify variations of essential genes in metabolic networks that were missed using traditional approaches.

This novel form of intermediate expression, when used in addition to traditional methods, can offer scientists a more colorful palette of options; beyond off and on, scientists can determine the level of gene expression by the gradations.

The Impact

Metabolic engineering could lead to sustainable pathways for making high-value bioproducts including biofuels. In addition, the team says that this experiment outlines a roadmap that is transferable to other systems, expanding the technologies available for other JGI users outside the realm of bioenergy optimization.

Summary

Life is all about balance. This study, recently published in the Proceedings of the National Academy of Sciences (PNAS), offers more ways for scientists to explore the balance of gene expression and the observable characteristics in an organism.

The experiment was led by Hal Alper, professor and associate chair at the University of Texas, Austin, and included researchers at the U.S. Department of Energy (DOE) Joint Genome Institute (JGI), a DOE Office of Science User Facility located at Lawrence Berkeley National Laboratory (Berkeley Lab).

Researchers used a library-based approach to fine-tune gene expression. They tested this new methodology in yeast (Saccharomyces cerevisiae) to assess the potential of intermediate gene expression on two energy-filled sugars used in biofuel production, glycerol and galactose. Although they are historically well-studied, Alper’s team discovered new gene targets to more efficiently grow on these sugars.

To demonstrate the versatility of this novel technique, Alper and his team also applied this method to a production-based scenario, in this case, the production of betaxanthins. They used combinations of single guide RNA, or a single RNA piece that recognizes a particular area in the DNA, to determine which targets might benefit from an intermediate level of expression. Similar to the results of the sugar-related tests, they pinpointed multiple genes that were previously missed in knock-out screens. These results show that this singular library synthesized by JGI was versatile enough for use in multiple applications.

This proof-of-concept experiment offers a new approach for fine-tuning gene expression in metabolic pathways that could be used for biofuel optimization and other applications.

Contacts:

BER Contact
Ramana Madupu, Ph.D.
Program Manager, DOE Joint Genome Institute
Biological Systems Sciences Division
Office of Biological and Environmental Research
Office of Science
US Department of Energy
[email protected]

JGI Contact
Yasuo Yoshikuni
DNA Synthesis Science Program head
Joint Genome Institute
[email protected]

PI Contact
Hal Alper, Ph.D.
The University of Texas at Austin
[email protected]

Funding

This work was funded by the Air Force Office of Scientific Research under Award No. FA9550-14-1-0089, the Camille and Henry Dreyfus Foundation, and the JGI Synthesis Program under FP00005685. In addition, M.D. acknowledges funding from a National Defense Science and Engineering Graduate Fellowship. The work conducted by the U.S. Department of Energy Joint Genome Institute, a DOE Office of Science User Facility, is supported under Contract No. DE-AC02-05CH11231.

Publications

Bowman EK et al. Bi-directional Titration of Yeast Gene Expression using a Pooled CRISPR Guide RNA Approach. Proc Natl Acad Sci U S A. 2020 July. doi: 10.1073/pnas.2007413117