Vartiainen E, Palvimo J, Mahonen A, Linnala-Kankkunen A, Mäenpää P H
Department of Biochemistry, University of Kuopio, Finland.
FEBS Lett. 1988 Feb 8;228(1):45-8. doi: 10.1016/0014-5793(88)80581-7.
We have studied the presence of high-mobility-group (HMG) chromatin proteins in undifferentiated F9 mouse teratocarcinoma cells and F9 cells, which were induced to differentiate by treatment with retinoic acid and dibutyryl-cAMP for 5 days. Acetic acid/urea-polyacrylamide gel electrophoresis and reversed-phase HPLC revealed that the induced F9 cells contained 77 and 62% less HMG I and HMG Y, respectively, than their untreated counterparts. The relative amounts of two other low-Mr HMG proteins HMG 14 and HMG 17 remained essentially unchanged and only a minor decrease was observed in the content of one of the high-Mr HMG proteins, HMG 2. The identity of the low-Mr HMG proteins was verified by amino acid analysis or partial sequencing. These results suggest that HMG I and HMG Y are HMG proteins specific for undifferentiated cells.
我们研究了高迁移率族(HMG)染色质蛋白在未分化的F9小鼠畸胎瘤细胞以及经视黄酸和二丁酰环磷腺苷处理5天诱导分化的F9细胞中的存在情况。乙酸/尿素-聚丙烯酰胺凝胶电泳和反相高效液相色谱显示,诱导后的F9细胞中HMG I和HMG Y的含量分别比未处理的对应细胞少77%和62%。另外两种低分子量HMG蛋白HMG 14和HMG 17的相对含量基本保持不变,但仅观察到一种高分子量HMG蛋白HMG 2的含量略有下降。低分子量HMG蛋白的身份通过氨基酸分析或部分测序得以验证。这些结果表明,HMG I和HMG Y是未分化细胞特有的HMG蛋白。