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新型 VRK1 突变患者运动神经元中 Cajal 体的缺失。

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.

机构信息

Aix Marseille Univ, Inserm, MMG, U 1251, Marseille, France.

Unité de Génétique Médicale, Université Saint Joseph, Campus des Sciences Médicales, Beirut, Lebanon.

出版信息

Hum Mol Genet. 2019 Jul 15;28(14):2378-2394. doi: 10.1093/hmg/ddz060.

Abstract

Distal hereditary motor neuropathies (dHMNs) are a heterogeneous group of diseases, resembling Charcot-Marie-Tooth syndromes, but characterized by an exclusive involvement of the motor part of the peripheral nervous system. Here, we describe two new compound heterozygous mutations in VRK1, the vaccinia-related kinase 1 gene, in two siblings from a Lebanese family, affected with dHMN associated with upper motor neurons (MNs) signs. The mutations lead to severely reduced levels of VRK1 by impairing its stability, and to a shift of nuclear VRK1 to cytoplasm. Depletion of VRK1 from the nucleus alters the dynamics of coilin, a phosphorylation target of VRK1, by reducing its stability through increased proteasomal degradation. In human-induced pluripotent stem cell-derived MNs from patients, we demonstrate that this drop in VRK1 levels leads to Cajal bodies (CBs) disassembly and to defects in neurite outgrowth and branching. Mutations in VRK1 have been previously reported in several neurological diseases affecting lower or both upper and lower MNs. Here, we describe a new phenotype linked to VRK1 mutations, presenting as a classical slowly progressive motor neuropathy, beginning in the second decade of life, with associated upper MN signs. We provide, for the first time, evidence for a role of VRK1 in regulating CB assembly in MNs. The observed MN defects are consistent with a length dependent axonopathy affecting lower and upper MNs, and we propose that diseases due to mutations in VRK1 should be grouped under a unique entity named `VRK1-related motor neuron disease'.

摘要

远端遗传性运动神经病(dHMNs)是一组异质性疾病,类似于腓骨肌萎缩症,但特征是仅累及周围神经系统的运动部分。在这里,我们描述了 VRK1 基因中的两个新的复合杂合突变,VRK1 是一种痘苗相关激酶,存在于一对来自黎巴嫩家庭的受影响 dHMN 伴有上运动神经元(MNs)迹象的兄弟姐妹中。这些突变通过损害其稳定性严重降低 VRK1 的水平,并导致核 VRK1 向细胞质移位。通过增加蛋白酶体降解,VRK1 从核内耗竭会改变 VRK1 的磷酸化靶标 coilin 的动力学。在患者来源的人诱导多能干细胞衍生的 MN 中,我们证明这种 VRK1 水平下降导致 Cajal 体(CB)解体,并导致轴突生长和分支缺陷。以前已经在几种影响下或上下 MN 的神经疾病中报道了 VRK1 突变。在这里,我们描述了一种与 VRK1 突变相关的新表型,表现为经典的缓慢进行性运动神经病,始于生命的第二个十年,伴有上 MN 迹象。我们首次提供了 VRK1 在调节 MN 中的 CB 组装中的作用的证据。观察到的 MN 缺陷与影响下和上 MN 的长度依赖性轴索病变一致,我们提出由于 VRK1 突变引起的疾病应归为一个名为“VRK1 相关运动神经元疾病”的独特实体。

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