Development, structure, and maintenance of C. elegans body wall muscle.

Kathrin Gieseler, Hiroshi Qadota, Guy M Benian
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引用次数: 10

Abstract

In C. elegans, mutants that are defective in muscle function and/or structure are easy to detect and analyze since: 1) body wall muscle is essential for locomotion, and 2) muscle structure can be assessed by multiple methods including polarized light, electron microscopy (EM), Green Fluorescent Protein (GFP) tagged proteins, and immunofluorescence microscopy. The overall structure of the sarcomere, the fundamental unit of contraction, is conserved from C. elegans to man, and the molecules involved in sarcomere assembly, maintenance, and regulation of muscle contraction are also largely conserved. This review reports the latest findings on the following topics: the transcriptional network that regulates muscle differentiation, identification/function/dynamics of muscle attachment site proteins, regulation of the assembly and maintenance of the sarcomere by chaperones and proteases, the role of muscle-specific giant protein kinases in sarcomere assembly, and the regulation of contractile activity, and new insights into the functions of the dystrophin glycoprotein complex.

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秀丽隐杆线虫体壁肌肉的发育、结构和维持。
在秀丽隐杆线虫中,肌肉功能和/或结构缺陷的突变体很容易检测和分析,因为:1)体壁肌肉是运动所必需的,2)肌肉结构可以通过多种方法进行评估,包括偏振光,电子显微镜(EM),绿色荧光蛋白(GFP)标记蛋白和免疫荧光显微镜。作为收缩的基本单位,肌节的整体结构从秀丽隐杆线虫到人类都是保守的,参与肌节组装、维持和肌肉收缩调节的分子也在很大程度上是保守的。本文综述了以下方面的最新发现:调节肌肉分化的转录网络,肌肉附着位点蛋白的识别/功能/动力学,伴侣蛋白和蛋白酶对肌节组装和维持的调节,肌肉特异性巨蛋白激酶在肌节组装中的作用,收缩活性的调节,以及对肌营养不良蛋白糖蛋白复合物功能的新见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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