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Defective Gene Slows Down Brain Cells in People with Autism

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Within the EU alone, about three million people are affected by an autism spectrum disorder (ASD). Some are only mildly affected and can live independent lives. Others have severe disabilities. What the different forms have in common is difficulty with social interaction and communication, as well as repetitive-stereotypic behaviours.

Mutations in a few hundred genes are associated with ASD. One of them is called Cullin 3, and it is a high-risk gene – a mutation of this gene almost certainly leads to a disorder. But how exactly does this gene affect the brain? To learn more about it, Jasmin Morandell and Lena Schwarz, PhD students in Professor Gaia Novarino’s research group, turned to mice whose Cullin 3 gene has been partially deactivated and compared them to their healthy siblings. Their results have just been published in the journal Nature Communications.

In a series of behavioural and motoric tests, the team wanted to see if the modified mice mimicked some characteristics of patients with this form of autism and could, therefore, be used as model organisms. In one of these tests, the so-called three-chamber sociability test, a mouse could freely explore three adjacent chambers of a box connected by little doors. Now, the scientists put two other mice in the outer boxes: One was already familiar to the studied mouse, and the other mouse it had never met. ‘Healthy mice usually prefer the new over the already familiar mouse,’ Jasmin Morandell, co-first author of the study, explains. The mouse with the altered Cullin 3 gene, however, showed no sign of recognition. Furthermore, the mice had motor coordination deficits as well as other ASD-relevant cognitive impairments. With the help of this mouse model, the team was then able to get to the bottom of the mechanisms that bring about these changes.

A dangerous accumulation of proteins

While studying the mouse brain, the researchers noticed a very subtle, but consistent, change in the position of some brain cells. These so-called neurons or nerve cells originate from a special region in the brain. From there, they migrate toward the uppermost layers until they find their designated place in the cortex. It is a very sensitive process, where even small changes in the speed at which they travel can change the structure of the cortex. By marking the migrating neurons, scientists could trace their movements. ‘We could observe migration deficits – the neurons are stranded in the lower cortex layers,’ Lena Schwarz, the other co-first author of the study, describes. But why are the cells not moving as they should?

The answer lies in the important role Cullin 3 plays at the end of the life of proteins. When their time has come, the gene Cullin 3 tags them for degradation – a process that has to be tightly regulated to prevent proteins from accumulating. To find out which proteins are misregulated when Cullin 3 is defective, Morandell and Schwarz systematically analysed the protein composition of the mouse brain. ‘We were looking at proteins that accumulate in the mutant brain and found a protein called Plastin 3. Then Gaia came across a poster describing the work of IST Austria’s Schur group in the hallway, and we got very excited,’ says Jasmin Morandell. ‘They independently had been working on Plastin 3 as a regulator of cell motility and had complementary results to ours. That’s when we started working together,’ Professor Gaia Novarino remembers.

It turned out that the protein, Plastin 3, which was previously unknown in the context of neuronal cell migration, actually plays an important role in this process. ‘If the Cullin 3 gene is deactivated, the Plastin 3 protein accumulates, causing cells to migrate slower and over shorter distances. This is exactly what we saw happening in the cortex of the Cullin 3 mutant mice,’ said PhD student Lena Schwarz.

A risky pathway?

All this is taking place during a very early stage of brain development around halfway through pregnancy – long before anyone would notice any difference in the foetus. ‘Determining these critical windows during brain development could be extremely important to fine-tune the treatment of patients with specific forms of ASD,’ explains Novarino, who is committed to improving diagnosis and treatment options for people with ASD. ‘Following up with the research on Plastin 3 could pave the way for some therapeutics. Inhibiting the accumulation of this protein could eventually alleviate some symptoms patients have,’ Schwarz says.

‘We now know that defective Cullin 3 leads to increased levels of Plastin 3. This tight correlation shows that Plastin 3 protein levels may be an important factor for the control of cell-intrinsic movements,’ said Jasmin Morandell. She recently graduated and may use her expertise in brain development to study Huntington’s disease. Lena Schwarz will next turn to additional high-risk ASD genes to see how other proteins in the degradation pathway may be linked to ASD. For the present study, the Novarino group joined forces with the Danzl and Schur groups and a colleague from the University of Rome. ‘Finishing this extensive study in around two and a half years despite the pandemic was only possible with the support from our neighbours at IST Austria,’ Novarino praises the multidisciplinarity at the Institute.

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