Ye Jianwei, Zhang Yong, Xu Jialin, Zhang Qiang, Zhu Dahai
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, 5 Dong Dan San Tiao, Beijing 100005, PR China.
Gene. 2007 Dec 1;404(1-2):53-60. doi: 10.1016/j.gene.2007.08.020. Epub 2007 Sep 7.
F-box proteins are key components of SCF (Skp1-Cullin1-F-box protein) complexes, which exert E3 ubiquitin ligase activity and participate in cell cycle and signal transduction. F-box proteins interact with Skp1 through the F-box domain and with proteins to be ubiquitinated through other interaction domains. We have characterized a novel muscle-specific F-box protein, FBXO40, the expression of which decreases in the dystrophic muscle of Limb-girdle muscular dystrophy (LGMD) patient. During the development of skeletal muscle, FBXO40 can only be detected at postnatal stage from about 2 weeks after birth. By overexpressing in C2C12 cells, FBXO40 localized in cytoplasm. Most importantly, the expression of FBXO40 can be upregulated in skeletal muscle from denervation- but not starvation-related muscle atrophy. All our data suggest that FBXO40 may function as a regulator involved in the postnatal myogenesis.
F-box蛋白是SCF(Skp1-Cullin1-F-box蛋白)复合物的关键组成部分,该复合物具有E3泛素连接酶活性,并参与细胞周期和信号转导。F-box蛋白通过F-box结构域与Skp1相互作用,并通过其他相互作用结构域与待泛素化的蛋白质相互作用。我们鉴定了一种新型的肌肉特异性F-box蛋白FBXO40,其在肢带型肌营养不良(LGMD)患者的营养不良肌肉中的表达降低。在骨骼肌发育过程中,FBXO40仅在出生后约2周的出生后阶段才能检测到。通过在C2C12细胞中过表达,FBXO40定位于细胞质中。最重要的是,FBXO40的表达在去神经支配而非饥饿相关的肌肉萎缩的骨骼肌中可以上调。我们所有的数据表明,FBXO40可能作为一种参与出生后肌生成的调节因子发挥作用。