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TRIP12 E3结合酶诱导SWI/SNF组件BRG1-β-catenin相互作用以促进Wnt信号传递
Sara Kassel1, Kai Yuan2, Nawat Bunnag2,3
1Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Nature communications
|June 5, 2025
概括
这就是Wnt信号通路.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
背景情况:
- SWI/SNF复合体为基因转录重塑染色质.
- SWI/SNF复合体对于发育和癌症至关重要.
- 连接信号通路与SWI/SNF招募的机制尚不清楚.
研究的目的:
- 为了阐明Wnt/β-catenin通路如何招募SWI/SNF复合体.
- 通过Wnt信号来调查SWI/SNF招募中无处不在的作用.
主要方法:
- 在各种模型生物和细胞系中TRIP12的耗尽.
- 遗传经验的实验.遗传经验实验.
- 同免疫沉和无处不在测试.
- 对BRG1和β-catenin相互作用的分析.
主要成果:
- 通过TRIP12介导的BRG1无处不在对于Wnt目标基因激活至关重要.
- 在β-catenin破坏复合体下游的 TRIP12 功能.
- 在Wnt通路激活时,TRIP12促进BRG1与β-catenin结合.
- 减少TRIP12会影响多种物种的Wnt信号传输.
结论:
- TRIP12作为BRG1的泛素化酶,促进SWI/SNF对Wnt目标基因的招募.
- 这种依赖于无处不在的机制提供了Wnt信号和染色质重塑之间的联系.
- 这些发现表明,信号诱导的SWI/SNF通过蛋白质-蛋白质相互作用招募的一般模型.
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