Washington State University researchers have seen how a particular gene is involved in the quality of sleep experienced by three different animals, including humans. The gene and its function open a new avenue for scientists exploring how sleep works and why animals need it so badly. “Sleep must be serving some important function, but as scientists we still don’t understand what that is,” said Jason Gerstner, assistant research professor in WSU’s Elson S. Floyd College of Medicine and lead author of a paper in the journal Science Advances.

“One way to get closer to that is by understanding how it is regulated or what processes exist that are shared across species.”

As a doctoral student at the University of Wisconsin, Gerstner looked at genes that change expression over the sleep–wake cycle and found expression of the gene FABP7 changed over the day throughout the brain of mice. He and colleagues saw that mice with a knocked out FABP7 gene slept more fitfully compared to mice with the gene intact. This suggested the gene is required for normal sleep in mammals.

To see if FABP7 is indeed required for normal sleep in humans, Gerstner and colleagues in Japan looked at data from nearly 300 Japanese men who underwent a seven–day sleep study that included an analysis of their DNA. It turned out that 29 of them had a variant of the gene responsible for the production of FABP7.

Like the mice, they tended to sleep more fitfully. While they would get the same amount of sleep as other people, their sleep was not as good, with more waking events when they should be sleeping.

Finally, the researchers made transgenic fruit flies. They inserted mutated and normal human FABP7 genes into star–shaped glial cells called astrocytes. Glial cells were long thought to be mere supporting characters to neurons, the processors of information in the brain. But researchers more recently have found that, like neurons, glial cells release chemical neurotransmitters and control behavior.

To monitor the flies’ sleep, the researchers used a commercial “Drosophila activity monitor” that automatically records activity changes using an infrared beam to determine if a fly is awake or asleep. If the beam is unbroken for five or more minutes, the machine concludes the fly is asleep.

It turned out that flies with the mutated FABP7 gene broke the beam more frequently during the normal sleep time. Like mice and humans without a properly functioning FABP7 gene, mutant FABP7 flies slept more fitfully.

“This suggests that there’s some underlying mechanism in astrocytes throughout all these species that regulates consolidated sleep,” said Gerstner.

FABP7 proteins are involved in what is called “lipid signaling,” shuttling fats to a cell nucleus to activate genes controlling growth and metabolism. Gerstner and his colleagues will now look to see how these functions might intersect with theories about why sleep matters. Among those theories are that sleep is important for neuronal activity, energy use and storage, and memory and learning.

Gerstner’s collaborators include scientists in Japan, Wisconsin and Pennsylvania, as well as WSU research intern Samantha Riedy, WSU professor Marcos Frank, and Hans Van Dongen, director of the WSU Sleep and Performance Research Center.