Peters M F, Adams M E, Froehner S C
Department of Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7545, USA.
J Cell Biol. 1997 Jul 14;138(1):81-93. doi: 10.1083/jcb.138.1.81.
The syntrophins are a multigene family of intracellular dystrophin-associated proteins comprising three isoforms, alpha1, beta1, and beta2. Based on their domain organization and association with neuronal nitric oxide synthase, syntrophins are thought to function as modular adapters that recruit signaling proteins to the membrane via association with the dystrophin complex. Using sequences derived from a new mouse beta1-syntrophin cDNA, and previously isolated cDNAs for alpha1- and beta2-syntrophins, we prepared isoform-specific antibodies to study the expression, skeletal muscle localization, and dystrophin family association of all three syntrophins. Most tissues express multiple syntrophin isoforms. In mouse gastrocnemius skeletal muscle, alpha1- and beta1-syntrophin are concentrated at the neuromuscular junction but are also present on the extrasynaptic sarcolemma. beta1-syntrophin is restricted to fast-twitch muscle fibers, the first fibers to degenerate in Duchenne muscular dystrophy. beta2-syntrophin is largely restricted to the neuromuscular junction. The sarcolemmal distribution of alpha1- and beta1-syntrophins suggests association with dystrophin and dystrobrevin, whereas all three syntrophins could potentially associate with utrophin at the neuromuscular junction. Utrophin complexes immunoisolated from skeletal muscle are highly enriched in beta1- and beta2-syntrophins, while dystrophin complexes contain mostly alpha1- and beta1-syntrophins. Dystrobrevin complexes contain dystrophin and alpha1- and beta1-syntrophins. From these results, we propose a model in which a dystrophin-dystrobrevin complex is associated with two syntrophins. Since individual syntrophins do not have intrinsic binding specificity for dystrophin, dystrobrevin, or utrophin, the observed preferential pairing of syntrophins must depend on extrinsic regulatory mechanisms.
肌养蛋白是细胞内与肌营养不良蛋白相关的蛋白质的多基因家族,由三种亚型组成,即α1、β1和β2。基于其结构域组织以及与神经元型一氧化氮合酶的关联,肌养蛋白被认为作为模块化衔接蛋白发挥作用,通过与肌营养不良蛋白复合物的结合将信号蛋白招募至细胞膜。利用源自新的小鼠β1-肌养蛋白cDNA的序列以及先前分离的α1-和β2-肌养蛋白的cDNA,我们制备了亚型特异性抗体,以研究所有三种肌养蛋白的表达、骨骼肌定位以及与肌营养不良蛋白家族的关联。大多数组织表达多种肌养蛋白亚型。在小鼠腓肠肌中,α1-和β1-肌养蛋白集中于神经肌肉接头处,但也存在于突触外肌膜上。β1-肌养蛋白局限于快肌纤维,这是杜氏肌营养不良症中最早发生退化的纤维。β2-肌养蛋白主要局限于神经肌肉接头处。α1-和β1-肌养蛋白在肌膜上的分布表明它们与肌营养不良蛋白和肌营养不良素结合蛋白相关,而所有三种肌养蛋白在神经肌肉接头处都可能与抗肌萎缩蛋白相关。从骨骼肌中免疫分离出的抗肌萎缩蛋白复合物高度富含β1-和β2-肌养蛋白,而肌营养不良蛋白复合物主要包含α1-和β1-肌养蛋白。肌营养不良素结合蛋白复合物包含肌营养不良蛋白以及α1-和β1-肌养蛋白。基于这些结果,我们提出了一个模型,其中肌营养不良蛋白-肌营养不良素结合蛋白复合物与两种肌养蛋白相关。由于单个肌养蛋白对肌营养不良蛋白、肌营养不良素结合蛋白或抗肌萎缩蛋白没有内在的结合特异性,因此观察到的肌养蛋白的优先配对必定依赖于外在的调节机制。