PIN1 是一种新的相互作用伙伴,也是转录因子NFIB的负上游调节者
Sinem Saritas Erdogan1, Ahmet Erdal Yilmaz1, Asli Kumbasar1
1Department of Molecular Biology and Genetics, Istanbul Technical University, Turkey.
FEBS letters
|September 8, 2024
概括
基基异构酶PIN1以酸化依赖的方式与转录因子NFIB结合. PIN1通过诱导形状变化来抑制NFIB活动,而不是通过改变其丰度来抑制NFIB活动.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 发展生物学 发展生物学
背景情况:
- 核因子一 (NFI) 家族的转录因子,包括NFIB,对于胚胎发育至关重要.
- 对NFIB及其上游监管机构的翻译后监管在很大程度上仍然没有特征.
研究的目的:
- 调查NFIB的翻译后规则.
- 确定控制NFIB功能的新型监管机构和机制.
主要方法:
- 同免疫沉测试检测蛋白质与蛋白质相互作用.
- 对NFIB转录活动的分析.
- 位点定向的突变发生以探测功能域.
主要成果:
- PIN1以酸化依赖的方式通过其WW域绑定NFIB.
- PIN1相互作用减弱了NFIB转录活性,需要基质结合,但不需要异构酶活性.
- 矛盾的是,PIN1结合稳定了NFIB蛋白水平.
结论:
- 对于PIN1.1,NFIB是一种新型基质.
- PIN1通过形状变化抑制NFIB功能,而不是调节蛋白质丰度.
- PIN1在NFIB和其他NFI家族成员的翻译后控制中发挥作用.
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