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SRSF1 and hnRNP H antagonistically regulate splicing of COLQ exon 16 in a congenital myasthenic syndrome.SRSF1和hnRNP H在先天性肌无力综合征中对COLQ外显子16的剪接起拮抗调节作用。
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本文引用的文献

1
Limiting role of protein disulfide isomerase in the expression of collagen-tailed acetylcholinesterase forms in muscle.蛋白质二硫键异构酶在肌肉中胶原尾型乙酰胆碱酯酶形式表达中的限制作用
J Biol Chem. 2009 Nov 13;284(46):31753-63. doi: 10.1074/jbc.M109.038471. Epub 2009 Sep 16.
2
Scalable purification of adeno-associated virus serotype 1 (AAV1) and AAV8 vectors, using dual ion-exchange adsorptive membranes.使用双离子交换吸附膜可扩展纯化1型腺相关病毒(AAV1)和8型腺相关病毒(AAV8)载体。
Hum Gene Ther. 2009 Sep;20(9):1013-21. doi: 10.1089/hum.2009.006.
3
Dissociation of transcription, translation, and assembly of collagen-tailed acetylcholinesterase in skeletal muscle.骨骼肌中胶原尾型乙酰胆碱酯酶转录、翻译和组装的解离
J Biol Chem. 2009 Aug 7;284(32):21488-95. doi: 10.1074/jbc.M109.030049. Epub 2009 Jun 9.
4
Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy.层粘连蛋白-111蛋白疗法可预防杜氏肌营养不良症的mdx小鼠模型中的肌肉疾病。
Proc Natl Acad Sci U S A. 2009 May 12;106(19):7991-6. doi: 10.1073/pnas.0811599106. Epub 2009 Apr 28.
5
Myocyte enhancer factor 2 mediates acetylcholine-induced expression of acetylcholinesterase-associated collagen ColQ in cultured myotubes.肌细胞增强因子2介导培养的肌管中乙酰胆碱诱导的乙酰胆碱酯酶相关胶原ColQ的表达。
Mol Cell Neurosci. 2008 Nov;39(3):429-38. doi: 10.1016/j.mcn.2008.07.018. Epub 2008 Jul 31.
6
Evidence of a dosage effect and a physiological endplate acetylcholinesterase deficiency in the first mouse models mimicking Schwartz-Jampel syndrome neuromyotonia.在首批模拟施瓦茨-扬佩尔综合征神经肌强直的小鼠模型中,存在剂量效应及生理性终板乙酰胆碱酯酶缺乏的证据。
Hum Mol Genet. 2008 Oct 15;17(20):3166-79. doi: 10.1093/hmg/ddn213. Epub 2008 Jul 21.
7
Clinical gene therapy using recombinant adeno-associated virus vectors.使用重组腺相关病毒载体的临床基因治疗。
Gene Ther. 2008 Jun;15(11):858-63. doi: 10.1038/gt.2008.68. Epub 2008 Apr 17.
8
Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.COLQ 基因突变所致先天性肌无力综合征的临床及分子遗传学发现
Brain. 2008 Mar;131(Pt 3):747-59. doi: 10.1093/brain/awm325. Epub 2008 Jan 7.
9
AAV vectors and tumorigenicity.腺相关病毒载体与致瘤性。
Nat Biotechnol. 2007 Oct;25(10):1111-3. doi: 10.1038/nbt1007-1111.
10
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease.细胞锚定减少可能导致乌尔里希病中肌膜特异性胶原蛋白VI缺乏。
Neurology. 2007 Sep 4;69(10):1043-9. doi: 10.1212/01.wnl.0000271386.89878.22.

将乙酰胆碱酯酶递送到神经肌肉接头的蛋白锚定策略。

Protein-anchoring strategy for delivering acetylcholinesterase to the neuromuscular junction.

机构信息

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

出版信息

Mol Ther. 2012 Jul;20(7):1384-92. doi: 10.1038/mt.2012.34. Epub 2012 Feb 28.

DOI:10.1038/mt.2012.34
PMID:22371845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3392993/
Abstract

Acetylcholinesterase (AChE) at the neuromuscular junction (NMJ) is anchored to the synaptic basal lamina via a triple helical collagen Q (ColQ). Congenital defects of ColQ cause endplate AChE deficiency and myasthenic syndrome. A single intravenous administration of adeno-associated virus serotype 8 (AAV8)-COLQ to Colq(-/-) mice recovered motor functions, synaptic transmission, as well as the morphology of the NMJ. ColQ-tailed AChE was specifically anchored to NMJ and its amount was restored to 89% of the wild type. We next characterized the molecular basis of this efficient recovery. We first confirmed that ColQ-tailed AChE can be specifically targeted to NMJ by an in vitro overlay assay in Colq(-/-) mice muscle sections. We then injected AAV1-COLQ-IRES-EGFP into the left tibialis anterior and detected AChE in noninjected limbs. Furthermore, the in vivo injection of recombinant ColQ-tailed AChE protein complex into the gluteus maximus muscle of Colq(-/-) mice led to accumulation of AChE in noninjected forelimbs. We demonstrated for the first time in vivo that the ColQ protein contains a tissue-targeting signal that is sufficient for anchoring itself to the NMJ. We propose that the protein-anchoring strategy is potentially applicable to a broad spectrum of diseases affecting extracellular matrix molecules.

摘要

乙酰胆碱酯酶(AChE)在神经肌肉接头(NMJ)处通过三螺旋胶原 Q(ColQ)锚定在突触基底膜上。ColQ 的先天性缺陷会导致终板 AChE 缺乏和肌无力综合征。将腺相关病毒血清型 8(AAV8)-COLQ 单次静脉内给药给 Colq(-/-)小鼠,恢复了运动功能、突触传递以及 NMJ 的形态。ColQ 尾巴的 AChE 被特异性地锚定在 NMJ 上,其数量恢复到野生型的 89%。接下来,我们对这种高效恢复的分子基础进行了表征。我们首先通过 Colq(-/-)小鼠肌肉切片的体外覆盖测定证实 ColQ 尾巴的 AChE 可以被特异性地靶向 NMJ。然后,我们将 AAV1-COLQ-IRES-EGFP 注入左胫骨前肌,并在未注射的肢体中检测到 AChE。此外,将重组 ColQ 尾巴的 AChE 蛋白复合物体内注射到 Colq(-/-)小鼠的臀大肌中,导致 AChE 在未注射的前肢中积累。我们首次在体内证明 ColQ 蛋白含有一个组织靶向信号,足以将自身锚定到 NMJ。我们提出,这种蛋白锚定策略可能适用于广泛的影响细胞外基质分子的疾病。