Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Institute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, 50931 Cologne, Germany; Center for Molecular Medicine Cologne, University of Cologne, 50931 Cologne, Germany.
Am J Hum Genet. 2020 Dec 3;107(6):1078-1095. doi: 10.1016/j.ajhg.2020.11.002. Epub 2020 Nov 19.
The myosin-directed chaperone UNC-45B is essential for sarcomeric organization and muscle function from Caenorhabditis elegans to humans. The pathological impact of UNC-45B in muscle disease remained elusive. We report ten individuals with bi-allelic variants in UNC45B who exhibit childhood-onset progressive muscle weakness. We identified a common UNC45B variant that acts as a complex hypomorph splice variant. Purified UNC-45B mutants showed changes in folding and solubility. In situ localization studies further demonstrated reduced expression of mutant UNC-45B in muscle combined with abnormal localization away from the A-band towards the Z-disk of the sarcomere. The physiological relevance of these observations was investigated in C. elegans by transgenic expression of conserved UNC-45 missense variants, which showed impaired myosin binding for one and defective muscle function for three. Together, our results demonstrate that UNC-45B impairment manifests as a chaperonopathy with progressive muscle pathology, which discovers the previously unknown conserved role of UNC-45B in myofibrillar organization.
肌球蛋白导向伴侣 UNC-45B 对于从秀丽隐杆线虫到人骨骼肌的肌节组织和肌肉功能至关重要。UNC-45B 在肌肉疾病中的病理影响仍然难以捉摸。我们报告了 10 名 UNC45B 双等位基因突变的个体,他们表现为儿童期起病的进行性肌肉无力。我们鉴定了一个常见的 UNC45B 变体,它作为一个复杂的功能降低剪接变体。纯化的 UNC-45B 突变体显示折叠和溶解度的变化。原位定位研究进一步表明,突变 UNC-45B 在肌肉中的表达减少,与肌节 A 带的异常定位远离,朝向 Z 盘。通过转基因表达保守的 UNC-45 错义变体,我们在秀丽隐杆线虫中研究了这些观察结果的生理相关性,其中一个变体显示肌球蛋白结合受损,三个变体显示肌肉功能缺陷。总之,我们的结果表明 UNC-45B 功能障碍表现为一种伴侣蛋白病,伴有进行性肌肉病理,揭示了 UNC-45B 在肌原纤维组织中的以前未知的保守作用。