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The Ever Plastic Brain and Intellectual Disabilities


The plasticity of the brain is always somewhat of a shock. It’s near incredible what the brain can achieve, look at people who have strokes, or any other sort of brain injury and yet still somehow manage to get up and move, or perform tasks. So I guess it should be no surprise, but still amazing that studying mice with a genetic change similar to what is found in Kabuki syndrome (an inherited disease of humans) researchers report they have used an anticancer drug to improve mental function.

Along with a potential treatment for the intellectual disability seen in Kabuki syndrome, the study’s findings also suggest a new way of thinking about a category of genetic diseases known as Mendelian disorders of the epigenetic machinery.

So what exactly is Kabuki syndrome? Well for those who did not click the link, in these disorders, a genetic mutation causes errors in the way proteins and chemicals bind to DNA. This in turn affects the rate at which DNA make proteins. In the case of the Kabuki syndrome-like condition the mice had, the researchers found that those errors lead to a persistent but treatable decrease in new cell growth in one part of the brain. Their study adds to the growing evidence that intellectual disability may not always be irreversible.

“Mendelian disorders of the epigenetic machinery affect how cells ‘package’ and use DNA, so they tend to have complicated and far-reaching effects,” says Hans Bjornsson, M.D., Ph.D. “Finding that a drug can ease some of the symptoms in this group of disorders suggests that other Mendelian disorders of the histone machinery may be treated in a similar manner.”

The research focuses particularly on Kabuki syndrome, which is caused by mutations in one of two genes that govern proteins that DNA wrap around, but may have many other applications. DNA wound around the packaging proteins is known as chromatin; only by forming chromatin can several feet of DNA fit inside the tiny command centers of each cell. But in order for a cell to read the DNA and put it to use making new proteins of its own, the chromatin must temporarily open up.

Specialized enzymes, often called “writers” and “erasers,” add or subtract chemical groups to the packaging proteins to help induce the chromatin to open or close. In recent years, other researchers have found that Kabuki syndrome can be caused by mutations to one of two genes—one for a writer, one for an eraser—with the same net effect on chromatin opening. That finding led the group to suspect that Kabuki syndrome and similar conditions might be caused by an imbalance between chromatin’s open and closed states.

If true, that would mean that disorders of the histone machinery could be treated by altering the balance between open and closed states. To test the idea, researchers used mice with a mutation in one of the Kabuki syndrome genes and a condition similar to Kabuki syndrome.

When the mice were at their young adult phase, the team treated them with AR-42, a drug developed for cancers of the blood which was found to open up compacted chromatin. After two weeks of treatment, they put the mice through a drill called the Morris water maze, which tests their ability to form memories in a region of the brain called the hippocampus. The treated mice performed better than the untreated mice with the Kabuki-like condition—about as well as healthy mice.

Studying the brains of the treated mice, the researchers saw that compared to untreated peers, they had more newly formed neurons in a part of the hippocampus called the dentate gyrus.

“The dentate gyrus is important for memory formation, and it’s also one of the few places in adult brains where we see new neurons,” Bjornsson says. “We think that when DNA’s chromatin open up, the cells are able to ‘turn up’ one or more genes needed for that new growth.”

Physicians generally consider the intellectual disability that accompanies disorders like Kabuki syndrome to be irreversible.

“But we now know that new brain cells continue to form throughout our lives. If Kabuki syndrome and related disorders cause fewer neurons to be made in adulthood, stimulating neuron growth may be an effective strategy for treating intellectual disability,” he says.

This isn’t the only genetic condition that has had advances. In fact, a Scottish research group has reported a way to reverse neurological dysfunction in mice with a condition similar to Rett syndrome, an inherited disorder that also causes intellectual disability.

A treatment for any inborn intellectual disability in people—including Kabuki syndrome—could still take a decade or even more to develop. The next steps will be to home in on the dentate gyrus to see whether it really is the main source of the memory defect found in the Kabuki mice and to explore whether there are other potential drugs that have a similar effect.

Proving once again we cannot underestimate the power of the brain. It’s a clever little design and is far more robust than we have historically given it credit for being. But really, the brains plasticity is paramount to our survival so this may highlight just how good of an architect nature can be.

Hans T. Bjornsson, Joel S. Benjamin, Li Zhang, Jacqueline Weissman, Elizabeth E. Gerber, Yi-Chun Chen, Rebecca G. Vaurio, Michelle C. Potter, Kasper D. Hansen, & Harry C. Dietz (2014). Histone deacetylase inhibition rescues structural and functional brain deficits in a mouse model of Kabuki syndrome Science Translational Medicine : 10.1126/scitranslmed.3009278


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