通过无素依赖的翻译调节来确定细胞命运
Achim Werner1,2, Shintaro Iwasaki2, Colleen A McGourty2
1Howard Hughes Medical Institute, University of California, Berkeley, California 94720, USA.
Nature
|September 25, 2015
概括
通过修改Treacher Collins综合征中涉及的蛋白质来调节神经细胞的特异性. 这一过程通过无素依赖的翻译调节影响细胞命运的确定.
科学领域:
- 细胞生物学
- 发育生物学
- 生物化学
背景情况:
- 甲基动物的发育依赖于多能干细胞精确分化为特定的细胞命运.
- 虽然染色体和转录变化是已知的调节剂,但支持细胞命运决定的其他事件不太了解.
研究的目的:
- 确定神经的新型调节剂.
- 阐明在细胞酸盐的确定中所起的作用.
主要方法:
- 在人类和Xenopus tropicalis模型中研究了CUL3的功能.
- 分析了NOLC1和TCOF1蛋白质的无处不在.
- 研究了无处不在对TCOF1-NOLC1复合体和转化重编程的影响.
主要成果:
- 确定CUL3 ((KBTBD8) 对于神经的规范至关重要.
- 一个与Treacher Collins综合征相关的基因 - - NOLC1和TCOF8.
- TCOF1-NOLC1的泛基化创建了一个将RNA聚合酶I连接到核糖体修饰酶的平台,改变了转化程序.
结论:
- 在细胞命运的确定中,依赖于ubiquitin的翻译调节是关键机制.
- 在神经的规范过程中,CUL3 ((KBTBD8) 在调节转化场景方面发挥着关键作用.
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