Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20126 Milan, Italy.
Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago 60611, IL, USA.
Brain. 2023 Jul 3;146(7):2730-2738. doi: 10.1093/brain/awad068.
ATP5F1B is a subunit of the mitochondrial ATP synthase or complex V of the mitochondrial respiratory chain. Pathogenic variants in nuclear genes encoding assembly factors or structural subunits are associated with complex V deficiency, typically characterized by autosomal recessive inheritance and multisystem phenotypes. Movement disorders have been described in a subset of cases carrying autosomal dominant variants in structural subunits genes ATP5F1A and ATP5MC3. Here, we report the identification of two different ATP5F1B missense variants (c.1000A>C; p.Thr334Pro and c.1445T>C; p.Val482Ala) segregating with early-onset isolated dystonia in two families, both with autosomal dominant mode of inheritance and incomplete penetrance. Functional studies in mutant fibroblasts revealed no decrease of ATP5F1B protein amount but severe reduction of complex V activity and impaired mitochondrial membrane potential, suggesting a dominant-negative effect. In conclusion, our study describes a new candidate gene associated with isolated dystonia and confirms that heterozygous variants in genes encoding subunits of the mitochondrial ATP synthase may cause autosomal dominant isolated dystonia with incomplete penetrance, likely through a dominant-negative mechanism.
ATP5F1B 是线粒体 ATP 合酶或线粒体呼吸链复合物 V 的一个亚基。核基因编码组装因子或结构亚基的致病性变异与复合物 V 缺乏有关,通常表现为常染色体隐性遗传和多系统表型。携带结构亚基基因 ATP5F1A 和 ATP5MC3 中常染色体显性变异的一部分病例中已经描述了运动障碍。在这里,我们报告了在两个家族中鉴定出两种不同的 ATP5F1B 错义变异(c.1000A>C;p.Thr334Pro 和 c.1445T>C;p.Val482Ala)与早发性孤立性肌张力障碍共分离,均具有常染色体显性遗传模式和不完全外显率。在突变成纤维细胞中的功能研究表明,ATP5F1B 蛋白量没有减少,但复合物 V 活性严重降低,线粒体膜电位受损,提示存在显性负效应。总之,我们的研究描述了一个与孤立性肌张力障碍相关的新候选基因,并证实编码线粒体 ATP 合酶亚基的基因中的杂合变异可能导致不完全外显率的常染色体显性孤立性肌张力障碍,可能通过显性负机制。