A new kind of congenital disorder caused by a group of mutations in a gene previously linked only to a rare progressive brain disease has been discovered by an international team co-led by Saudi investigators.
The disorder—congenital hypotonia, epilepsy, developmental delay, digit abnormalities, or CHEDDA—is characterized by intellectual disability, reduced muscle tone and facial abnormalities. It results from defects in ATN1, a gene also implicated in a neurodegenerative condition called dentatorubral-pallidoluysian atrophy (DRPLA). However, the disease-causing mutations responsible for each illness occur in different regions of the gene, and the clinical symptoms of DRPLA and CHEDDA are observably distinct.
The discovery stems from a collaboration between two clinical geneticists—Fowzan Alkuraya of King Faisal Specialist Hospital and Research Center in Saudi Arabia and Emma Palmer from Sydney Children’s Hospital in Australia—each of whom had a young patient with a mysterious condition suspected to arise from ATN1 mutations.
To understand the origin of the novel disorder, the clinicians contacted KAUST structural biologist, Stefan Arold and his group at the Computational Bioscience Research Center to analyze their patients’ mutations on a molecular level. Although the CHEDDA-affected children did not have the exact same genetic defect, Arold’s team found that all mutations disrupted the same stretch of the protein encoded by ATN1—one contained an unusual repetitive structure, which they named the HX repeat motif.
Follow-up studies conducted with KAUST teams led by cell biologist Jasmeen Merzaban and structural biologists Mariusz Jaremko and Łukasz Jaremko further uncovered the function of this enigmatic motif and how CHEDDA-related gene variants alter its molecular characteristics. The KAUST researchers also identified similar motifs encoded by a handful of other genes linked to cognitive disorders, suggesting that the team may have discovered a mutational mechanism of broad clinical significance.
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