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在先天性肌弛缓综合征中,DOK7 的突变在培养细胞中形成聚集物,并降低患者来源的 iPS 细胞中 DOK7 的表达和 MuSK 的磷酸化。

A mutation in DOK7 in congenital myasthenic syndrome forms aggresome in cultured cells, and reduces DOK7 expression and MuSK phosphorylation in patient-derived iPS cells.

机构信息

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, Japan.

出版信息

Hum Mol Genet. 2023 Apr 20;32(9):1511-1523. doi: 10.1093/hmg/ddac306.

Abstract

At the neuromuscular junction, the downstream of tyrosine kinase 7 (DOK7) enhances the phosphorylation of muscle-specific kinase (MuSK) and induces clustering of acetylcholine receptors (AChRs). We identified a patient with congenital myasthenic syndrome (CMS) with two heteroallelic mutations in DOK7, c.653-1G>C in intron 5 and c.190G>A predicting p.G64R in the pleckstrin homology domain. iPS cells established from the patient (CMS-iPSCs) showed that c.653-1G>C caused in-frame skipping of exon 6 (120 bp) and frame-shifting activation of a cryptic splice site deleting seven nucleotides in exon 6. p.G64R reduced the expression of DOK7 to 10% of wild-type DOK7, and markedly compromised AChR clustering in transfected C2C12 myotubes. p.G64R-DOK7 made insoluble aggresomes at the juxtanuclear region in transfected C2C12 myoblasts and COS7 cells, which were co-localized with molecules in the autophagosome system. A protease inhibitor MG132 reduced the soluble fraction of p.G64R-DOK7 and enhanced the aggresome formation of p.G64R-DOK7. To match the differentiation levels between patient-derived and control induced pluripotent stem cells (iPSCs), we corrected c.190G>A (p.G64R) by CRISPR/Cas9 to make isogenic iPSCs while retaining c.653-1G>C (CMS-iPSCsCas9). Myogenically differentiated CMS-iPSCs showed juxtanuclear aggregates of DOK7, reduced expression of endogenous DOK7 and reduced phosphorylation of endogenous MuSK. Another mutation, p.T77M, also made aggresome to a less extent compared with p.G64R in transfected COS7 cells. These results suggest that p.G64R-DOK7 makes aggresomes in cultured cells and is likely to compromise MuSK phosphorylation for AChR clustering.

摘要

在神经肌肉接头处,酪氨酸激酶 7(DOK7)的下游增强肌肉特异性激酶(MuSK)的磷酸化,并诱导乙酰胆碱受体(AChR)的聚集。我们鉴定了一名患有先天性肌营养不良综合征(CMS)的患者,其 DOK7 存在两个异等位基因突变,5 号内含子中的 c.653-1G>C 和预测在pleckstrin 同源结构域中的 c.190G>A 导致 p.G64R。从患者中建立的诱导多能干细胞(iPSCs)表明,c.653-1G>C 导致外显子 6(120 bp)的框内跳跃,并激活外显子 6 中的一个隐匿剪接位点,该剪接位点缺失 7 个核苷酸。p.G64R 将 DOK7 的表达降低至野生型 DOK7 的 10%,并显著损害转染的 C2C12 肌管中的 AChR 聚集。p.G64R-DOK7 在转染的 C2C12 成肌细胞和 COS7 细胞的核周区形成不可溶的聚集物,与自噬体系统中的分子共定位。蛋白酶抑制剂 MG132 减少了 p.G64R-DOK7 的可溶性部分,并增强了 p.G64R-DOK7 的聚集物形成。为了使患者来源的和对照诱导多能干细胞(iPSCs)之间的分化水平相匹配,我们通过 CRISPR/Cas9 纠正了 c.190G>A(p.G64R),同时保留了 c.653-1G>C(CMS-iPSCsCas9),从而构建了同基因 iPSCs。肌源性分化的 CMS-iPSCs 显示 DOK7 的核周聚集物,内源性 DOK7 的表达减少,内源性 MuSK 的磷酸化减少。另一个突变 p.T77M 与 p.G64R 相比,在转染的 COS7 细胞中也形成聚集物的程度较小。这些结果表明,p.G64R-DOK7 在培养细胞中形成聚集物,并且可能会损害 MuSK 磷酸化以进行 AChR 聚集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5594/10117378/f08849dc3308/ddac306f1.jpg

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