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USP10通过双重使用duebiquitinase活性和相分离潜力打击β-catenin
Yinuo Wang1, Aihua Mao2, Jingwei Liu3
1College of Life and Health Science, Northeastern University, Shenyang 110819, China.
Cell chemical biology
|August 23, 2023
概括
USP10二维基因酶调节了Wnt/β-catenin信号传递. 它通过deubiquitination稳定Axin1并促进相分离,抑制β-catenin在发育,平衡和结直肠癌中的作用.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 生物化学 生物化学
背景情况:
- Wnt/β-catenin信号传递对发育,平衡和癌症至关重要.
- 识别这种途径的调节者对于基础和转化研究至关重要.
研究的目的:
- 为了确定Wnt/β-catenin信号传递的新型调节者.
- 阐明USP10调节这种通路的机制.
主要方法:
- 蛋白质查以确定调节器.
- 生物化学测试以确定脱化活性.
- 同免疫沉和相分离试验.
- 在胚胎发育和结直肠癌模型中的体内研究.
主要成果:
- USP10被确定为β-catenin的一个关键调节器.
- USP10通过K48连接的二基化稳定了Axin1.
- USP10在物理上绑定了Axin1和β-catenin,促进了抑制β-catenin的相分离.
- USP10的双重功能 (酶和物理) 调节胚胎发育和肠道平衡.
- USP10抑制结直肠癌的生长,与Wnt/β-catenin水平相关.
结论:
- USP10表现出对Wnt/β-catenin信号传递的双重调节机制 (酶依赖和酶独立).
- 这些功能取决于上下文,并并行运行.
- USP10代表了Wnt/β-catenin驱动疾病的潜在治疗标.
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