Jun-Fos和维生素A和维生素D的受体在人类骨质卡尔基因中识别出一种共同的反应元素
R Schüle1, K Umesono, D J Mangelsdorf
1Howard Hughes Medical Institute, Salk Institute, La Jolla, California 92037.
Cell
|May 4, 1990
概括
骨质卡尔基因中的维生素D反应元件也对视网酸作出反应. 这种转录因子的交叉合揭示了维生素A和维生素D对基因调节的新见解.
科学领域:
- 分子生物学分子生物学
- 基因规则 基因规则
- 内分泌学 在内分泌学.
背景情况:
- 人类骨质卡尔基因含有维生素D反应元件 (VDRE).
- 维生素D和视网酸是关键的信号分子,参与各种细胞过程.
研究的目的:
- 调查VDRE在调解视网膜酸反应中的作用.
- 为了确定参与调节骨质卡尔基因表达的转录因子.
主要方法:
- 使用细菌表达的视网酸受体 (RAR) 的体外结合试验.
- 在体内研究涉及培养细胞中RAR表达载体的转染.
- 分析AP-1与Jun-Fos复合体的相互作用,以及共传染的影响.
主要成果:
- VDRE赋予了对视网酸的反应,证明了交叉合.
- 网红酸受体 (RAR) 在体外与VDRE序列结合.
- 与Jun和Fos的共同传染抑制了基底转录,并由视网酸和维生素D3诱导转录.
结论:
- 不同的转录因子类可以识别共同的调节序列 (交叉合).
- 在VDRE中的AP-1站点是多个因素的核心识别站点.
- 这一发现为维生素A和维生素D信号通路之间的交叉对话提供了新的见解.
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