Kametani Fuyuki, Nonaka Takashi, Suzuki Takehiro, Arai Tetsuaki, Dohmae Naoshi, Akiyama Haruhiko, Hasegawa Masato
Department of Molecular Neurobiology, Tokyo Institute of Psychiatry, Tokyo Metropolitan Organization for Medical Research, Tokyo, Japan.
Biochem Biophys Res Commun. 2009 May 1;382(2):405-9. doi: 10.1016/j.bbrc.2009.03.038. Epub 2009 Mar 13.
TAR DNA-binding protein of 43 kDa (TDP-43) is deposited as hyperphosphorylated cytoplasmic and intranuclear inclusions in brains of patients with frontotemporal lobar degeneration with ubiquitinated inclusions and amyotrophic lateral sclerosis. In this study, we identified 29 phosphorylation sites on recombinant TDP-43 that are phosphorylated by casein kinase-1 (CK1). Interestingly, 18 of them were located in the C-terminal glycine-rich region of TDP-43. Our results indicate that CK1-mediated phosphorylation may play a role in the pathogenesis of these diseases.
43 kDa的TAR DNA结合蛋白(TDP-43)以高度磷酸化的细胞质和核内包涵体形式沉积在患有泛素化包涵体的额颞叶变性和肌萎缩侧索硬化症患者的大脑中。在本研究中,我们鉴定出重组TDP-43上29个被酪蛋白激酶-1(CK1)磷酸化的磷酸化位点。有趣的是,其中18个位于TDP-43的C端富含甘氨酸区域。我们的结果表明,CK1介导的磷酸化可能在这些疾病的发病机制中起作用。