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- Title
<italic>ADGRV1</italic> is implicated in myoclonic epilepsy.
- Authors
Myers, Kenneth A.; Nasioulas, Steven; Boys, Amber; McMahon, Jacinta M.; Slater, Howard; Lockhart, Paul; Sart, Desirée du; Scheffer, Ingrid E.
- Abstract
Summary: Objective: To investigate the significance of variation in <italic>ADGRV1</italic> (also known as <italic>GPR98</italic>,<italic> MASS1</italic>, and <italic>VLGR1</italic>), <italic>MEF2C</italic>, and other genes at the 5q14.3 chromosomal locus in myoclonic epilepsy. Methods: We studied the epilepsy phenotypes of 4 individuals with 5q14.3 deletion and found that all had myoclonic seizures. We then screened 6 contiguous genes at 5q14.3, <italic>MEF2C, CETN3</italic>,<italic> MBLAC2</italic>,<italic> POLR3G</italic>,<italic> LYSMD3</italic>, and <italic>ADGRV1</italic>, in a 95‐patient cohort with epilepsy and myoclonic seizures. Of these genes, point mutations in <italic>MEF2C</italic> cause a phenotype involving seizures and intellectual disability. A role for <italic>ADGRV1</italic> in epilepsy has been proposed previously, based on a recessive mutation in the Frings mouse model of audiogenic seizures, as well as a shared homologous region with another epilepsy gene, <italic>LGI1</italic>. Results: Six patients from the myoclonic epilepsy cohort had likely pathogenic ultra‐rare <italic>ADGRV1</italic> variants, and statistical analysis showed that ultra‐rare variants were significantly overrepresented when compared to healthy population data from the Genome Aggregation Database. Of the remaining genes, no definite pathogenic variants were identified. Significance: Our data suggest that the <italic>ADGRV1</italic> variation contributes to epilepsy with myoclonic seizures, although the inheritance pattern may be complex in many cases. In patients with 5q14.3 deletion and epilepsy, <italic>ADGRV1</italic> haploinsufficiency likely contributes to seizure development. The latter is a shift from current thinking, as <italic>MEF2C</italic> haploinsufficiency has been considered the main cause of epilepsy in 5q14.3 deletion syndrome. In cases of 5q14.3 deletion and epilepsy, seizures likely occur due to haploinsufficiency of one or both of <italic>ADGRV1</italic> and <italic>MEF2C</italic>.
- Subjects
EPILEPSY; LOCUS (Genetics); PHENOTYPES; DELETION mutation; ANIMAL disease models
- Publication
Epilepsia (Series 4), 2018, Vol 59, Issue 2, p381
- ISSN
0013-9580
- Publication type
Article
- DOI
10.1111/epi.13980