Pathogenic variants of ADAM22 affecting either its biosynthesis and/or its interactions with either LGI1 and/or PSD-95 have been recently identified in individuals with developmental and epileptic encephalopathy. Here, we describe a girl with seizures, delayed psychomotor development, and behavioural disorder, carrying a homozygous variant in ADAM22 (NM_021723.5:c.2714C > T). The variant has a surprisingly high frequency in the Roma population of the Czech and Slovak Republic, with 11 of 213 (∼5.2%) healthy Roma individuals identified as heterozygous carriers. Structural in silico characterization revealed that the genetic variant encodes the missense variant p.S905F, which localizes to the PDZ-binding motif of ADAM22. Studies in transiently transfected mammalian cells revealed that the variant has no effect on biosynthesis and stability of ADAM22. Rather, protein-protein interaction studies showed that the p.S905F variant specifically impairs ADAM22 binding to PSD-95 and other proteins from a family of membrane-associated guanylate kinases, while it has only minor effect on ADAM22-LGI1 interaction. Our study indicates that a significant proportion of epilepsy in patients of Roma ancestry may be caused by homozygous c.2714C > T variants in ADAM22. The study of this ADAM22 variant highlights a novel pathogenic mechanism of ADAM22 dysfunction and reconfirms an essential role of interaction of ADAM22 with membrane-associated guanylate kinases in seizure protection in humans.
- Publikační typ
- časopisecké články MeSH
Autosomal-dominant adult-onset neuronal ceroid lipofuscinosis (ANCL) is characterized by accumulation of autofluorescent storage material in neural tissues and neurodegeneration and has an age of onset in the third decade of life or later. The genetic and molecular basis of the disease has remained unknown for many years. We carried out linkage mapping, gene-expression analysis, exome sequencing, and candidate-gene sequencing in affected individuals from 20 families and/or individuals with simplex cases; we identified in five individuals one of two disease-causing mutations, c.346_348delCTC and c.344T>G, in DNAJC5 encoding cysteine-string protein alpha (CSPα). These mutations-causing a deletion, p.Leu116del, and an amino acid exchange, p.Leu115Arg, respectively-are located within the cysteine-string domain of the protein and affect both palmitoylation-dependent sorting and the amount of CSPα in neuronal cells. The resulting depletion of functional CSPα might cause in parallel the presynaptic dysfunction and the progressive neurodegeneration observed in affected individuals and lysosomal accumulation of misfolded and proteolysis-resistant proteins in the form of characteristic ceroid deposits in neurons. Our work represents an important step in the genetic dissection of a genetically heterogeneous group of ANCLs. It also confirms a neuroprotective role for CSPα in humans and demonstrates the need for detailed investigation of CSPα in the neuronal ceroid lipofuscinoses and other neurodegenerative diseases presenting with neuronal protein aggregation.
- MeSH
- dominantní geny genetika MeSH
- dospělí MeSH
- exony genetika MeSH
- genetická vazba MeSH
- genová dávka genetika MeSH
- lidé MeSH
- lipoylace MeSH
- lyzozomy metabolismus ultrastruktura MeSH
- membránové proteiny genetika MeSH
- molekulární sekvence - údaje MeSH
- mozek metabolismus patologie ultrastruktura MeSH
- mutace genetika MeSH
- neuronální ceroidlipofuscinózy epidemiologie genetika patologie MeSH
- neurony metabolismus patologie ultrastruktura MeSH
- proteiny tepelného šoku HSP40 genetika MeSH
- regulace genové exprese MeSH
- rodina MeSH
- rodokmen MeSH
- segregace chromozomů genetika MeSH
- sekvence nukleotidů MeSH
- sekvenční analýza DNA MeSH
- transport proteinů MeSH
- věk při počátku nemoci MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- MeSH
- arteterapie * metody MeSH
- dětské nemocnice organizace a řízení využití MeSH
- kurikulum MeSH
- lidé MeSH
- mozková obrna * ošetřování rehabilitace terapie MeSH
- nemocnice pro chronická onemocnění organizace a řízení využití MeSH
- postižené děti * MeSH
- školy MeSH
- speciální vzdělávání metody MeSH
- výchova a vzdělávání metody MeSH
- Check Tag
- lidé MeSH
