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核膜、肌肉萎缩症与基因表达

The nuclear envelope, muscular dystrophy and gene expression.

作者信息

Wilson K L

机构信息

Dept of Cell Biology and Anatomy, The Johns Hopkins University School of Medicine, 725 N. Wolfe Street, Baltimore, MD 21205, USA.

出版信息

Trends Cell Biol. 2000 Apr;10(4):125-9. doi: 10.1016/s0962-8924(99)01708-0.

Abstract

Lamins and other nuclear envelope proteins organize nuclear architecture through structural attachments that vary dynamically during the cell cycle and cell differentiation. Genetic studies have now shown that people with mutations in either lamins A/C or emerin, a nuclear membrane protein, develop Emery-Dreifuss muscular dystrophy. A mouse model for this rare disease has been created by knocking out the gene that encodes lamin A/C. This article discusses these and other recent results in the wider context of nuclear envelope function, as a framework for thinking about the possible ways in which defects in nuclear envelope proteins can lead to disease.

摘要

核纤层蛋白和其他核膜蛋白通过在细胞周期和细胞分化过程中动态变化的结构连接来组织核结构。遗传学研究现已表明,核纤层蛋白A/C或核膜蛋白emerin发生突变的人会患上埃默里-德赖富斯肌营养不良症。通过敲除编码核纤层蛋白A/C的基因,已创建了这种罕见疾病的小鼠模型。本文在核膜功能的更广泛背景下讨论了这些以及其他近期研究结果,作为思考核膜蛋白缺陷可能导致疾病的方式的框架。

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