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一种新的 VPS11 杂合变异可能导致全身性肌张力障碍。

A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia.

机构信息

Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.

Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

出版信息

Ann Neurol. 2021 Apr;89(4):834-839. doi: 10.1002/ana.26021. Epub 2021 Feb 2.

Abstract

In this work, we describe the association of a novel homozygous VPS11 variant with adult-onset generalized dystonia, providing a detailed clinical report and biological evidence of disease mechanism. Vps11 is a subunit of the homotypic fusion and protein sorting (HOPS) complex, which promotes the fusion of late endosomes and autophagosomes with the lysosome. Functional studies on mutated fibroblasts showed marked lysosomal and autophagic abnormalities, which improved after overexpression of the wild type Vps11 protein. In conclusion, a deleterious VPS11 variant, damaging the autophagic and lysosomal pathways, is the probable genetic cause of a novel form of generalized dystonia. ANN NEUROL 2021;89:834-839.

摘要

在这项工作中,我们描述了一种新型 VPS11 变异与成人发病的全身性肌张力障碍的关联,提供了详细的临床报告和疾病机制的生物学证据。Vps11 是同源融合和蛋白质分选(HOPS)复合物的一个亚基,促进晚期内体和自噬体与溶酶体融合。对突变成纤维细胞的功能研究表明,溶酶体和自噬体存在明显异常,而过表达野生型 Vps11 蛋白后则有所改善。总之,具有破坏性的 VPS11 变异可能是一种新型全身性肌张力障碍的遗传原因,破坏了自噬和溶酶体途径。神经病学年鉴 2021;89:834-839.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e44/8048445/f2543a5b4d4c/ANA-89-834-g003.jpg

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