Kikuchi K, Sekikawa M, Imoto M, Tsuchiya T, Tsuda M
Faculty of Pharmaceutical Sciences, Okayama University, Japan.
Nucleic Acids Res. 1988 Nov 11;16(21):10171-81. doi: 10.1093/nar/16.21.10171.
To determine the role of protein phosphorylation in transcription regulation, we have treated mouse neuroblastoma N18TG2 cells with the protein kinase inhibitor H-7 and tested its effect on transcription. After the preculture and transfection in the presence of H-7, the cell preparation was divided in half and cultured with and without H-7. The level of CAT expression of pSV2-CAT was found to be higher in the cells cultured in the absence of H-7 than in those cultured in the presence of H-7. This difference was observed only after pretreatment of the cells with H-7, suggesting that withdrawal of H-7 from the culture medium after preculture with H-7 gave an enhancing effect on CAT expression. This phenomenon was also observed with transformants that expressed the CAT gene of pSV2-CAT stably. The 72 base-pair (bp) repeat of SV40 DNA was responsible for this difference in CAT expression. A similar effect of H-7 on the SV40 enhancer activity was observed in mouse neuroblastoma x rat glioma hybrid NG108-15 cells, but not in rat glioma C6-BU-1 cells.
为了确定蛋白质磷酸化在转录调控中的作用,我们用蛋白激酶抑制剂H - 7处理小鼠神经母细胞瘤N18TG2细胞,并测试其对转录的影响。在H - 7存在的情况下进行预培养和转染后,将细胞制剂分成两半,分别在有和没有H - 7的条件下培养。发现pSV2 - CAT的CAT表达水平在无H - 7培养的细胞中高于有H - 7培养的细胞。这种差异仅在细胞用H - 7预处理后才观察到,表明在用H - 7预培养后从培养基中去除H - 7对CAT表达有增强作用。在稳定表达pSV2 - CAT的CAT基因的转化体中也观察到了这种现象。SV40 DNA的72碱基对(bp)重复序列导致了CAT表达的这种差异。在小鼠神经母细胞瘤×大鼠胶质瘤杂交NG108 - 15细胞中观察到H - 7对SV40增强子活性有类似作用,但在大鼠胶质瘤C6 - BU - 1细胞中未观察到。