To check out seizures, ‘knock-in’ genes

BROWN (US) — Scientists have created fruit flies with a gene mutation analogous to one that causes epileptic seizures in people—a first in genetic engineering.

The researchers have created the Drosophila fruit fly model of epilepsy to discern the mechanism by which temperature-dependent (febrile) seizures happen.


The researchers used a technique called homologous recombination—a more precise and sophisticated technique than transgenic gene engineering—to give flies a disease-causing mutation that is a direct analogue of the mutation that leads to febrile epileptic seizures in humans.

They observed the temperature-dependent seizures in whole flies and also observed the process in the flies’ brains. What they discovered is that the mutation leads to a breakdown in the ability of certain cells that normally inhibit brain over-activity to properly regulate their electrochemical behavior.

“This is the first time anyone has introduced a human disease-causing mutation overtly into the same gene that flies possess,” says Robert Reenan, professor of biology at Brown University and a co-corresponding author of the paper in the Journal of Neuroscience.

Electrical failure

Homologous recombination (HR) starts with the transgenic technique of harnessing a transposable element or “jumping gene” to insert a specially mutated gene just anywhere into the fly’s DNA, but then goes beyond that to ultimately place the mutated gene into exactly the same position as the natural gene on the X chromosome.

HR does this by outfitting the gene to be handled by the cell’s own DNA repair mechanisms, essentially tricking the cell into putting the mutant copy into exactly the right place.

The new paper is a result of Reenan’s collaboration with neurobiologist Diane O’Dowd of University of California, Irvine. Reenan and undergraduate Jeff Gilligan used HR to insert a mutated version of the para gene in fruit flies that is a direct parallel of the mutation in the human gene SCN1A that causes febrile seizures in people.

When the researchers placed flies in tubes and bathed the tubes in 104-degree F water, the mutant fruit flies had seizures after 20 seconds, in which their legs began twitching followed by wing-flapping, abdominal-curling, and an inability to remain standing. After that, they remained motionless for as long as half an hour before recovering. Unaltered flies, meanwhile, exhibited no temperature-dependent seizures.

The researchers also found that seizure susceptibility was dose-dependent. Female flies with mutant strains of both copies of the para gene (females have two copies of the X chromosome) were the most susceptible to seizures. Those in which only one copy of the gene was a mutant were less likely than those with two to seize, but more likely than the controls.

While the researchers at Brown compared the seizure susceptibility of whole flies, O’Dowd, lead author Lei Sun, and colleagues at UC Irvine studied individual fly neurons implicated in seizure activity to see how they behaved as the brains were heated.

What their measurements revealed in the mutant flies were flaws in how “GABAergic” neurons take in sodium through channels in the cell membrane. Under normal circumstances, the neurons inhibit brain over-activity. But the mutants’ mishandling of sodium led them to fail electrically.

“When [O’Dowd’s team] isolates those currents due to the sodium channel, which is what’s mutated in this case, and she compares the normal animals to the disease-model animals, what happens is the mutant channels pass too much current,” Reenan says. “The channels open too easily and they take more effort to close. They open too soon and they close too late. That effect is magnified at higher temperature. Then the neuron can’t send any [inhibitory] signals.”

The ‘knock-in’ method

With a useful genetic model of epilepsy in fruit flies, Reenan says he is optimistic that researchers can now look for potential treatments for the disease. The next step, he says, is to use the practice of “forward genetics” to look for further mutations that might counter febrile seizures.

Given thousands of flies with a model of the disease, scientists can purposely subject them to different DNA-altering conditions and then look to see if any flies lose their propensity for seizures. Among those that do, the researchers can then identify the specific genetic alteration responsible and determine whether that could ever be clinically applied.

For example, if it turns out that a mutation proves therapeutic because it causes a certain protein to be over-expressed, then perhaps that protein could be refined into some kind of biologic pharmaceutical.

Reenan says he’d expect to see researchers follow a similar roadmap for other diseases as well.

“Knock-in of specific disease-causing mutations into the fly genome has the potential to provide a rapid and low-cost platform for studying the cellular mechanisms of heritable human diseases,” the authors write. “In addition, knock-in flies can be used in combination with forward genetic screens to identify suppressor and/or enhancer mutations, a strategy that is challenging in humans and rodent models but well established in Drosophila.”

The National Institutes of Health, the Howard Hughes Medical Institute, and the Ellison Medical Foundation funded the research.

Source: Brown University