生物
移码突变
无意义介导的衰变
外显子组测序
少突胶质细胞
胡说
神经发育障碍
遗传学
分子生物学
细胞生物学
髓鞘
基因
突变
神经科学
RNA剪接
核糖核酸
中枢神经系统
作者
Elizabeth A. Werren,Guillermo Rodríguez Bey,Purvi Majethia,Parneet Kaur,Siddaramappa J. Patil,Minal Kekatpure,Alexandra Afenjar,Leila Qebibo,Lydie Bürglen,Hoda Tomoum,Florence Démurger,Christele Duborg,Shahyan Siddiqui,Yao-Chang Tsan,Uzma Abdullah,Zafar Ali,Saadia Maryam Saadi,Shahid Mahmood Baig,Henry Houlden,Reza Maroofian,Quasar Saleem Padiath,Stephanie Bielas,Anju Shukla
出处
期刊:Brain
[Oxford University Press]
日期:2024-09-18
标识
DOI:10.1093/brain/awae299
摘要
Erythrocyte Membrane Protein Band 4.1 Like 3 (EPB41L3: NM_012307.5), also known as DAL-1, encodes the ubiquitously expressed, neuronally enriched 4.1B protein, part of the 4.1 superfamily of membrane-cytoskeleton adaptors. 4.1B plays key roles in cell spreading, migration, and cytoskeletal scaffolding that support oligodendrocyte axon adhesions essential for proper myelination. We herein describe six individuals from five unrelated families with global developmental delay, intellectual disability, seizures, hypotonia, neuroregression, and delayed myelination. Exome sequencing identified biallelic variants in EPB41L3 in all affected individuals: two nonsense (c.466C>T, p.(R156*); c.2776C>T, p.(R926*)) and three frameshift (c.666delT, p.(F222Lfs*46); c.2289dupC, p.(V764Rfs*19); c.948_949delTG, p.(A317Kfs*33)). Quantitative-real time PCR and Western blot analysis in human fibroblasts harbouring EPB41L3:c.666delT, p.(F222Lfs*46) indicate ablation of EPB41L3 mRNA and 4.1B protein expression. Inhibition of the nonsense mediated decay (NMD) pathway led to an upregulation of EPB41L3:c.666delT transcripts, supporting NMD as a pathogenic mechanism. Epb41l3-deficient mouse oligodendroglia cells showed significant reduction in mRNA expression of key myelin genes, reduced branching, and increased apoptosis. Our report provides the first clinical description of an autosomal recessive disorder associated with variants in EPB41L3, which we refer to as EPB41L3-associated developmental disorder (EADD). Moreover, our functional studies substantiate the pathogenicity of EPB41L3 hypothesized loss-of-function variants.