Horiguchi Ryo, Yoshikuni Michiyasu, Tokumoto Mika, Nagahama Yoshitaka, Tokumoto Toshinobu
Department of Molecular Biomechanics, The Graduate University for Advanced Studies, Okazaki 444-8585, Japan.
Cell Signal. 2005 Feb;17(2):205-15. doi: 10.1016/j.cellsig.2004.07.002.
The proteasome is involved in the progression of the meiotic cell cycle in fish oocytes. We reported that the alpha4 subunit of the 26S proteasome, which is a component of the outer rings of the 20S proteasome, is phosphorylated in immature oocytes and dephosphorylated in mature oocytes. To investigate the role of the phosphorylation, we purified the protein kinase from immature oocytes using a recombinant alpha4 subunit as substrate. A protein band which well corresponded to the kinase activity was identified as casein kinase Ialpha (CKIalpha). Two-dimensional (2D) PAGE analysis showed that part of the alpha4 subunit was phosphorylated by CKIalpha in vitro. This spot was detected in purified immature 26S proteasome but not in mature 26S proteasome, demonstrate that the alpha4 subunit is phosphorylated by CKIalpha meiotic cell cycle dependently.
蛋白酶体参与鱼类卵母细胞减数分裂细胞周期的进程。我们报道过,26S蛋白酶体的α4亚基(它是20S蛋白酶体外环的一个组成部分)在未成熟卵母细胞中被磷酸化,而在成熟卵母细胞中去磷酸化。为了研究磷酸化的作用,我们以重组α4亚基为底物,从未成熟卵母细胞中纯化出蛋白激酶。一条与激酶活性高度对应的蛋白条带被鉴定为酪蛋白激酶Iα(CKIα)。二维(2D)聚丙烯酰胺凝胶电泳分析表明,α4亚基的一部分在体外被CKIα磷酸化。这个斑点在纯化的未成熟26S蛋白酶体中被检测到,但在成熟26S蛋白酶体中未被检测到,这表明α4亚基在减数分裂细胞周期中依赖于CKIα被磷酸化。