Study Reveals a Rare Form of Autism

Study focused on the gene tied to a rare form of autism spectrum disorder called FOXP1 syndrome offers hope of gene therapy to help patients
Study focused on the gene tied to a rare form of autism spectrum disorder called FOXP1 syndrome offers hope of gene therapy to help patients.
(Representative image: Pixabay)
Study focused on the gene tied to a rare form of autism spectrum disorder called FOXP1 syndrome offers hope of gene therapy to help patients. (Representative image: Pixabay)
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A new study focused on the gene tied to a rare form of autism spectrum disorder (ASD) called FOXP1 syndrome offers hope that gene therapy might be able to help patients with this condition.

In a study published in Science Advances, researchers from UT Southwestern Medical Center found that using gene therapy to restore the Foxp1 gene to adult mice from which it had been deleted before birth restored the activity of other genes whose levels are controlled by Foxp1. This intervention also corrected some abnormal behaviors characteristic of mice that lack Foxp1. The findings could shed light on other forms of ASD as well.

The ability to partially remedy brain pathway changes at later developmental stages suggests that gene therapy may be effectively applied in FOXP1 syndrome and actually normalize symptoms.

Genevieve Konopka, Ph.D., Professors of Neuroscience

“The ability to partially remedy brain pathway changes at later developmental stages suggests that gene therapy may be effectively applied in FOXP1 syndrome and actually normalize symptoms,” said Genevieve Konopka, Ph.D., who co-led the study with Jay Gibson, Ph.D. Both are Professors of Neuroscience and Investigators in the Peter O’Donnell Jr. Brain Institute at UT Southwestern.

About 200 individuals worldwide have FOXP1 syndrome, a genetic condition caused by mutations in the FOXP1 gene that render it nonfunctional. Along with intellectual deficits, developmental delays, and other symptoms, people with this disease also tend to have ASD or exhibit autistic behaviors. But how the loss of FOXP1 contributes to these symptoms has been unclear, Dr. Gibson explained.

Along with intellectual deficits, developmental delays, and other symptoms, people with this disease also tend to have ASD or exhibit autistic behaviors.
(Representative image: Pixabay)
Along with intellectual deficits, developmental delays, and other symptoms, people with this disease also tend to have ASD or exhibit autistic behaviors. (Representative image: Pixabay)

A key circuit that’s disrupted in FOXP1 syndrome connects regions of the brain called the cortex, thalamus, and striatum. To better understand FOXP1’s involvement in this circuit, Drs. Konopka and Gibson and their colleagues used a technique to delete this gene in mice in two populations of neurons in the striatum, which receives inputs from both the cortex and thalamus through a chemical called glutamate. Glutamate causes these neurons to fire when it’s taken up at structures called synapses that connect neurons.

In one population of neurons, the deletion altered the functions of thousands of other genes and caused changes in neuronal responses as well as significant differences in behavior; the animals had problems building nests and spent more time on the edges of their enclosures. When the researchers used a genetic technique to reinstate Foxp1, this intervention normalized how neurons responded to glutamate and restored activity in 78 genes, most known to function in neural synapses. It also normalized some behaviors, such as nesting and time spent in enclosures. 

Further study of this gene and the thousands of other genes it regulates could identify new targets for pharmaceuticals to treat this condition. 
(Representative image: Pixabay)
Further study of this gene and the thousands of other genes it regulates could identify new targets for pharmaceuticals to treat this condition. (Representative image: Pixabay)

Further study of this gene and the thousands of other genes it regulates could identify new targets for pharmaceuticals to treat this condition. Because some of these genes have also been implicated in other forms of ASD, continuing to study FOXP1 could lead to a better understanding and potential treatments for ASD in general, Dr. Konopka noted.

(NewsWise/YVH)

Study focused on the gene tied to a rare form of autism spectrum disorder called FOXP1 syndrome offers hope of gene therapy to help patients.
(Representative image: Pixabay)
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