结合GC盒诱导由DNA依赖的蛋白激酶对Sp1进行酸化
S P Jackson1, J J MacDonald, S Lees-Miller
1Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley 94720.
Cell
|October 5, 1990
概括
SV40感染触发了Sp1酸化,这是早期基因转录至关重要的修饰. 这种酸化依赖于DNA,这表明了转录启动的新型调节机制.
科学领域:
- 分子生物学分子生物学
- 基因规则 基因规则
- 病毒学 病毒学
背景情况:
- 猿人病毒40 (SV40) 早期基因的有效转录取决于转录因子Sp1.1.
- 众所周知,SV40感染会诱导宿主和病毒因子的修饰.
研究的目的:
- 在SV40感染期间调查转录因子Sp1的酸化.
- 描述负责Sp1酸化的激酶及其调节机制.
主要方法:
- 试管体内转录试验用于研究Sp1酸化.
- 细胞分离和柱状染色学以确定Sp1激酶.
- 对酸化所需的Sp1域进行分析.
主要成果:
- SV40感染诱导了Sp1酸化.
- 在实验室中,Sp1经历了定量,多重的过程性酸化.
- 酸化取决于Sp1与GC盒DNA的结合.
- Sp1激酶是一种核DNA结合蛋白,被确定为一种DNA依赖蛋白激酶.
- 有效的Sp1酸化需要功能性的DNA结合和转录激活域.
结论:
- Sp1属于转录因子的一个特定子组,在促进体结合时被化.
- Sp1的DNA结合合酸化代表了调节转录启动的新机制.
- 这一发现提供了关于病毒基因表达的复杂调节的见解.
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