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FBXO40是一种编码新型肌肉特异性F-box蛋白的基因,在去神经支配相关的肌肉萎缩中上调。

FBXO40, a gene encoding a novel muscle-specific F-box protein, is upregulated in denervation-related muscle atrophy.

作者信息

Ye Jianwei, Zhang Yong, Xu Jialin, Zhang Qiang, Zhu Dahai

机构信息

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.

出版信息

Gene. 2007 Dec 1;404(1-2):53-60. doi: 10.1016/j.gene.2007.08.020. Epub 2007 Sep 7.

Abstract

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.

摘要

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。

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