Whole exome sequencing identifies variable expressivity of CLN6 variants in Progressive myoclonic epilepsy affected families

• Published in: Epilepsy research 2024-03, Vol.201, p.107283-107283, Article 107283
• Main Authors: Ilyas, Muhammad, Tariq, Faiza, Ishaq, Rafaqat, Habiba, Umme, Bibi, Farah, Khan, Sadiq Noor, Ali, Yasir, Haider, Shehzad, Efthymiou, Stephanie, Abdullah, Uzma, Raja, Ghazala Kaukab, Shaiq, Pakeeza Arzoo
• Format: Article
• Language: English
• Subjects: CLN6; Neuronal ceroid lipofuscinosis; Progressive myoclonic epilepsies
• ISSN: 0920-1211; 1872-6844
• DOI: 10.1016/j.eplepsyres.2023.107283

Progressive myoclonic epilepsies (PMEs) are a group of neurodegenerative disorders, predominantly affecting adolescents and, characterized by generalized worsening myoclonus epilepsies, ataxia, cognitive deficits, and dementia. To date, several genes, having implications in diverse phenotypic expressions associated with PMEs, have been identified. Genetic diagnosis is available for most of the adolescence-onset myoclonic epilepsies. This study aimed to elucidate the genetic basis of PMEs in three multiplex Pakistani families exhibiting clinically variable phenotypes. Causative variant(s) in the studied families, and mode of segregation were identified by Whole Exome Sequencing (WES) of the probands, followed by bi-directional Sanger sequencing for final validation. We identified homozygous recessive CLN6 missense variant c.768 C>G (p.Asp256Glu) in Family 1, and c.889 C>A (p.Pro297Thr) variant in Family 2. While in Family 3, we found a homozygous variant (c.316dup) that caused a frameshift mutation, leading to a premature stop codon in the CLN6 protein, resulting in a truncated protein (p.Arg106ProfsTer26). Though CLN6 is previously identified to underlie late infantile and adolescent onset neuronal ceroid lipofuscinosis, this study supports and expands the phenotypic spectrum of CLN6 mutations and signifies diagnositc potential CLN6 variants for PMEs. Diverse pathological effects of variant c .768 C>G were observed in Family 1, with same genotypes, suggesting clinical heterogeneity and/or variable expressivity that might be the implication of pleiotropic effects of the gene in these cases. •This study uncovers the genetic basis of Progressive Myoclonic Epilepsies (PMEs) in three Pakistani families with varying clinical presentations.•Whole Exome Sequencing (WES) is employed for precise genetic diagnosis of PMEs in the affected individuals.•Homozygous recessive mutations in the CLN6 gene (c .768 C>G, c .889 C>A, and c.316dup) are identified, all linked to PMEs.•CLN6 mutations are shown to expand their clinical implications beyond neuronal ceroid lipofuscinosis, enhancing our understanding of their impact.•The study reveals clinical heterogeneity within Family 1, suggesting variable expressivity of CLN6 mutations, possibly due to pleiotropic gene effects.