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Systematic identification of disease genes for congenital malformations of the central nervous system

Subject Area Developmental Neurobiology
Human Genetics
Term from 2019 to 2021
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 418099105
 
Final Report Year 2022

Final Report Abstract

Congenital malformations of the central nervous system (CNS) can affect the brain and/or the neural tube (neural tube defects, NTDs). CNS malformations present isolated (non-syndromic) or non-isolated (syndromic) as part of a genetic syndrome. The most common brain malformations include agenesis of the corpus callosum, holoprosencephaly, various forms of septo-optic dysplasia, lissencephaly, other malformations of cerebral cortical development, neuronal migration disorders, intacranial cysts and lipomas, encephaloceles, congenital hydrocephalus, various forms of Chiari malformation and Dandy Walker syndrome, and schizencephaly. These various brain malformations might present with a broad clinical spectrum. The most common form of NTDs, myelomeningocele, is an open lesion in the caudal spine and contains dysplastic spinal cord, often resulting in a lack of neural function below the level of the defect. Affected patients usually have reduced ability to walk, or need the use of a wheelchair, have little or no bowel and/or bladder control, and require frequent surgical interventions to minimize the effects of hydrocephalus. Here we performed large scale exome and genome sequencing in affected singletons and case-parent trios. We identified several highly prioritized coding and non-coding variants / candidate genes which we envisage to functionally characterize in vivo using zebrafish as a vertebrate model system. Having performed functional studies in zebrafish of PLXNA1 and SHROOM4 we were able to support both genes as disease genes with PLXNA1 being annotated in OMIM as a novel disease gene for the novel syndrome "DWORSCHAK-PUNETHA NEURODEVELOPMENTAL SYNDROME (DWOPNED) (# 619955)”. Regarding our functional studies in zebrafish of TFAP2E we believe that here we have also provided compelling evidence for this gene to be considered a disease-gene for a novel complex neurodevelopmental syndrome.

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