转录因子p62TCF通过MAP激酶的酸化刺激了在c-fos促进体的三元复合体形成
H Gille1, A D Sharrocks, P E Shaw
1Max-Planck-Institut für Immunbiologie, Spemann Laboratories, Freiburg, Germany.
Nature
|July 30, 1992
概括
线素激活蛋白 (MAP) 激酶酸化转录因子p62TCF,增强其与c-FOS基因促进体的结合. 这种酸化对于增长因子诱导的c-FOS基因表达至关重要.
科学领域:
- 分子生物学分子生物学
- 细胞信号传递 细胞信号传递
- 瘤基因是一种瘤基因.
背景情况:
- 原生瘤基因c-FOS转录由生长因子迅速诱导.
- 一个p67SRF和p62TCF的三元复合体结合了血清反应元素,这对于c-FOS诱导至关重要.
- 甲基因激活蛋白 (MAP) 激酶由甲基因激活,并传递增殖信号.
研究的目的:
- 调查MAP激酶在调节c-FOS转录中的作用.
- 为了确定MAP激酶是否直接影响c-FOS血清反应元素的三元复合体形成.
主要方法:
- 在实验室中使用MAP激酶和p62TCF进行酸化试验.
- 用表皮生长因子 (EGF) 和胰岛素刺激瑞士3T3细胞.
- 对c-FOS基因表达和三元复合体形成的分析.
主要成果:
- 在体外,MAP激酶酸化物p62TCF增强三元复合体的形成.
- EGF治疗激活MAP激酶,导致c-FOS表达和活跃的三元复合体形成.
- 不激活MAP激酶的胰岛素治疗无法诱导c-FOS转录或增强三元复合体的形成.
结论:
- 通过MAP激酶介导的p62TCF的酸化是增长因子诱导的c-FOS原型瘤基因表达的一个关键步骤.
- 这项研究将MAP激酶信号通路与c-FOS转录的调节联系起来.
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