Centro de Pesquisas sobre o Genoma Humano e Células-Tronco, Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.
Department of Cellular and Molecular Physiology, Pennsylvania State University, College of Medicine, Hershey, PA, 17033, USA.
Sci Rep. 2018 Jun 7;8(1):8706. doi: 10.1038/s41598-018-26818-2.
Whole-exome sequencing of samples from affected members of two unrelated families with late-onset non-syndromic hearing loss revealed a novel mutation (c.2090 T > G; NM_017433) in MYO3A. The mutation was confirmed in 36 affected individuals, showing autosomal dominant inheritance. The mutation alters a single residue (L697W or p.Leu697Trp) in the motor domain of the stereocilia protein MYO3A, leading to a reduction in ATPase activity, motility, and an increase in actin affinity. MYO3A-L697W showed reduced filopodial actin protrusion initiation in COS7 cells, and a predominant tipward accumulation at filopodia and stereocilia when coexpressed with wild-type MYO3A and espin-1, an actin-regulatory MYO3A cargo. The combined higher actin affinity and duty ratio of the mutant myosin cause increased retention time at stereocilia tips, resulting in the displacement of the wild-type MYO3A protein, which may impact cargo transport, stereocilia length, and mechanotransduction. The dominant negative effect of the altered myosin function explains the dominant inheritance of deafness.
对两个无血缘关系的迟发性非综合征性听力损失患者家族的受影响成员的样本进行外显子组测序,揭示了 MYO3A 中的一个新突变(c.2090 T > G;NM_017433)。该突变在 36 名受影响个体中得到证实,表现为常染色体显性遗传。该突变改变了动纤毛蛋白 MYO3A 运动域中的单个残基(L697W 或 p.Leu697Trp),导致 ATP 酶活性、运动性降低,肌动蛋白亲和力增加。MYO3A-L697W 在 COS7 细胞中表现出较少的丝状伪足肌动蛋白突起起始,并且当与野生型 MYO3A 和 espin-1(一种调节肌球蛋白的肌动蛋白货物)共表达时,在丝状伪足和静纤毛中优先向尖端聚集。突变肌球蛋白的结合更高的肌动蛋白亲和力和占空比导致在静纤毛尖端的保留时间增加,从而导致野生型 MYO3A 蛋白的位移,这可能影响货物运输、静纤毛长度和机械转导。改变的肌球蛋白功能的显性负效应解释了耳聋的显性遗传。