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单或双等位基因 ANK3 变异个体的表型和基因型谱。

The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants.

机构信息

Department of Epilepsy Genetics and Personalized Treatment, The Danish Epilepsy Centre, Dianalund, Denmark.

Faculty of Health Science, University of Southern Denmark (SDU), Odense, Denmark.

出版信息

Clin Genet. 2024 Nov;106(5):574-584. doi: 10.1111/cge.14587. Epub 2024 Jul 11.

Abstract

ANK3 encodes ankyrin-G, a protein involved in neuronal development and signaling. Alternative splicing gives rise to three ankyrin-G isoforms comprising different domains with distinct expression patterns. Mono- or biallelic ANK3 variants are associated with non-specific syndromic intellectual disability in 14 individuals (seven with monoallelic and seven with biallelic variants). In this study, we describe the clinical features of 13 additional individuals and review the data on a total of 27 individuals (16 individuals with monoallelic and 11 with biallelic ANK3 variants) and demonstrate that the phenotype for biallelic variants is more severe. The phenotypic features include language delay (92%), autism spectrum disorder (76%), intellectual disability (78%), hypotonia (65%), motor delay (68%), attention deficit disorder (ADD) or attention deficit hyperactivity disorder (ADHD) (57%), sleep disturbances (50%), aggressivity/self-injury (37.5%), and epilepsy (35%). A notable phenotypic difference was presence of ataxia in three individuals with biallelic variants, but in none of the individuals with monoallelic variants. While the majority of the monoallelic variants are predicted to result in a truncated protein, biallelic variants are almost exclusively missense. Moreover, mono- and biallelic variants appear to be localized differently across the three different ankyrin-G isoforms, suggesting isoform-specific pathological mechanisms.

摘要

ANK3 编码锚蛋白-G,一种参与神经元发育和信号传递的蛋白质。选择性剪接产生三种锚蛋白-G 同工型,它们包含不同的结构域,具有不同的表达模式。单等位基因或双等位基因 ANK3 变体与 14 名个体的非特异性综合征性智力残疾有关(7 名个体具有单等位基因变体,7 名个体具有双等位基因变体)。在这项研究中,我们描述了另外 13 名个体的临床特征,并回顾了总共 27 名个体(16 名个体具有单等位基因和 11 名具有双等位基因 ANK3 变体)的数据,证明双等位基因变体的表型更为严重。表型特征包括语言延迟(92%)、自闭症谱系障碍(76%)、智力残疾(78%)、张力减退(65%)、运动延迟(68%)、注意力缺陷障碍(ADD)或注意缺陷多动障碍(ADHD)(57%)、睡眠障碍(50%)、攻击性/自残(37.5%)和癫痫(35%)。值得注意的表型差异是,三名具有双等位基因变体的个体存在共济失调,但在具有单等位基因变体的个体中则没有。虽然大多数单等位基因变体预计会导致截短的蛋白质,但双等位基因变体几乎完全是错义的。此外,单等位基因和双等位基因变体似乎在三种不同的锚蛋白-G 同工型中定位不同,这表明存在同工型特异性的病理机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ef/11444875/3643d11c6d2b/nihms-2007393-f0002.jpg

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