Researchers healed mice with a genetic metabolic disorder that also affects humans by using a new editing tool to target and correct genetic mutations.
Some babies are born with the metabolic disorder phenylketonuria and need a special diet so that the amino acid phenylalanine doesn’t accumulate in the body. Excess phenylalanine delays mental and motor development. If left untreated, the children may develop mental disabilities.
The cause of this metabolic disorder is a mutation in a gene that provides the blueprint for the enzyme phenylalanine hydroxylase (Pah). The enzyme, which is produced by the cells of the liver, metabolizes phenylalanine.
The disorder is “autosomal recessive,” which means that the child develops the disease if it inherits one mutated gene from the mother and one from the father. There is no cure.
New editing technique
Now, researchers have taken advantage of a method that corrects both mutated genes in the liver cells and heals the disease. So far, they’ve succeeded, at least in mice.
With the help of a CRISPR/Cas9 system extended by one enzyme, the researchers changed the sequence of the DNA building blocks for the corresponding gene in adult mice. The liver cells were subsequently able to produce functioning Pah enzymes, and the mice healed.
Let’s look at the details: The CRISPR/Cas9 system enhanced by the enzyme cytidine deaminase binds to the locus on the gene that needs to be corrected and locally opens both DNA strands. The deaminase converts the disease-causing DNA base pair C-G into T-A, which is the base pair that occurs at that spot in healthy individuals. This corrects the error in the DNA sequence of the Pah enzyme.
In traditional CRISPR/Cas editing, inducing a DNA double-stranded break is the central element of genome editing. The double strand is cut at a defined point, and the cell attempts to repair the cut using various mechanisms. If researchers add a matching DNA sequence to the cell from outside, it enables a specialized repair mechanism to precisely modify the specific genetic sequence.
The problem here is that most human cells primarily use other DNA repair mechanisms that produce additional undesired mutations.
The researchers realized that the new genome editing tool is much more efficient than the traditional CRISPR/Cas9 method: with it they corrected up to 60 percent of all copies of the gene with errors in the mouse liver. This resulted in the concentration of phenylalanine falling to normal levels, and the animals no longer showing any signs of the disorder after getting treatment with the genome editing tool.
To transfer the genetic code for the new editing tool to the liver cells, the researchers implanted the required genes into adeno-associated viruses and injected them into the blood of the mice. The virus then infected the liver cells, thereby introducing the genes for the editing tool into the liver cell.
From mice to humans
“This approach has great potential for application in humans,” says Gerald Schwank, a professor at ETH Zurich. However, this study is only a first proof of concept. Clinical studies in other animal models would have to follow in order to test the efficacy and safety of the new genome editing tool for application in humans.
Previous methods of genome editing have only limited success at correcting target mutations directly in animals. The correction rate in the liver of adult mice has previously been only a few percent, explains Schwank. “Here we’ve achieved several fold higher editing rates—nobody has managed that so far.”
Schwank considers the risks to be low. After applying the editing tool in the mouse model the researchers looked for non-target mutations, that is, on sites where there shouldn’t be mutations. But they didn’t find any. Schwank would like to examine this more closely in a follow-up study.
“The human liver consists of several billion cells. In none of them we want to induce any mutations that could cause cancer,” emphasizes Schwank. Testing is also needed to find out whether the adeno-associated virus used by the researchers as a vehicle for applying the editing tool gene causes any adverse effects.
“The use of a base editor was the key to our success,” explains Lukas Villiger, Schwank’s doctoral candidate and the study’s primary author. Researchers developed the base editor at the Massachusetts Institute of Technology (MIT) and presented it two years ago in a scientific journal.
Before that, the ETH researchers had been working with traditional CRISPR/Cas approaches. In 2016, Schwank and Villiger starting using the techniques the US researchers had developed. “Even with the new base editors, the path still didn’t follow a straight line—we had to tinker around quite a bit”, says Villiger.
The biggest surprise was that this system is so much more effective than the traditional CRISPR/Cas toolbox.
Schwank is now looking for funding to conduct trails on other animal models such as pigs. “The liver of the mouse differs in size and structure from that of humans or pigs, so we definitely have to expand the scope of our trials to other organisms to make progress.”
Phenylketonuria is not the only genetic metabolic disorder that affects the liver. For example, urea cycle disorders prevent the body from removing ammonia (as a byproduct from foods containing nitrogen) from the blood and metabolizing it to urea. This results primarily in central nervous dysfunctions. The only currently available option to cure this disease is liver transplantation. Therefore, Schwank would like to test the newly developed genome editing tool for use in such diseases as well.
Source: ETH Zurich