Discovery of rules that govern a variation of the CRISPR/Cas9 gene-editing method makes it possible to use living cells to manufacture valuable metabolic compounds like pharmaceuticals and nutraceuticals. Researchers at Rensselaer Polytechnic Institute (RPI) have developed new tools for controlling the signaling pathways in cells to manufacture compounds, dialing down production of unwanted compounds, and increasing production of valuable compounds.
The research, published in Nucleic Acids Research, describes an aspect of the CRISPR/Cas9 gene-editing method, which makes use of dCas9, a disabled protein. Specifically, the researchers describe how to vary a snippet of RNA to create multiple tools that use dCas9, each with the ability to block activity at a single site along complex multi-step signaling pathways, with no crosstalk.
“CRISPR is one of the most powerful gene editing techniques available, but until now, we’ve only seen it used in healthcare. This is the first real metabolic engineering application to make high-value products using this gene editing approach,” said Mattheos Koffas, who led the research. “If you look 10 years into the future, people might be controlling thousands of genes in an organism, producing quite valuable products.”
The CRISPR/Cas9 system is derived from a natural defense bacteria employ against familiar viruses. “Clustered regularly interspaced short palindromic repeats,” or CRISPR, is bacterial DNA that contains segments of viral DNA from previous exposures. When known viral DNA invades the cell, bacteria use CRISPR to produce a snippet of “guide RNA” that will match with, or complement, the viral DNA. The guide RNA is coupled with the Cas9 protein complex, which can cut DNA. Thus equipped, the Cas9 is able to unzip, latch on, and cut the complementary viral DNA, thereby disabling it. CRISPR/Cas9 has been used in health applications, such as disabling specific genes to produce transgenic animals for research.
CRISPR/Cas9 also holds enormous potential as a means of controlling signaling pathways, the complex chemical communications by which cells perform most functions and make necessary substances. The instructions for the numerous steps in each signaling pathway are contained in DNA. If the process can be controlled at each step – by blocking or allowing transcription of DNA at the site of a genetic switch called a “promoter” – the output of the cell can also be controlled, redirecting its energy to producing desired compounds. One variation of this method, CRISPR/dCas9, blocks transcription by using a disabled Cas9 protein to latch on to the target DNA and remain in place, thwarting further attempts to transcribe the instructions in that particular DNA sequence.
“The cell is a factory, and we can take over production and make the things we want,” said Brady Cress, first author on the research, which was conducted in the labs of Koffas and Robert Linhardt in the Rensselaer Center for Biotechnology and Interdisciplinary Studies (CBIS). “With CRISPR/dCas9, what we can do is make critical compounds – those required to build up the big high-value compounds – more prevalent by shutting off competing pathways.”
Although the CRISPR method has great promise in metabolic engineering, a better understanding is needed to reach its full potential. One area of investigation involves the risk of “crosstalk,” a complication that occurs when target RNA intended for one promoter mistakenly binds to another promoter of similar sequence, causing it to activate or block other sections of the vastly complex pathways.
DNA is a chain composed of four nucleotides—cytosine, guanine, adenine, or thymine—each of which complements one of four RNA nucleotides. In order for the CRISPR/Cas9 system to latch on to DNA and perform its task, the nucleotides in the guide RNA sequence must complement the targeted DNA. But an exact match is not always necessary—one or more of the nucleotides can be incorrect and the guide RNA and target DNA might still adhere, albeit imperfectly. The rules that govern the degree of mismatch the system will support have not been clea