酶是通过蛋白质分解而不是通过激活成熟促进因子来启动的
S L Holloway1, M Glotzer, R W King
1Department of Physiology, University of California, San Francisco 94143-0444.
Cell
|July 2, 1993
概括
对于细胞分裂至关重要的姐妹染色体分离是由蛋白质降解引发的,而不是成熟促进因子 (MPF) 失活. 这个过程需要分解特定的蛋白质,而不仅仅是循环蛋白,以分离染色体.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 姐妹染色体分离是细胞分裂的一个关键事件,使染色体能够准确地分配给子细胞.
- 成熟促进因子 (MPF) 活性和环林降解是已知的线粒分裂的调节者,但对亚纳相的确切触发因素仍有争议.
研究的目的:
- 为了确定特定的分子事件,启动姐妹染色体分离在线粒分裂过程中.
- 为了研究MPF无活化和蛋白质降解在触发相中的作用.
主要方法:
- 使用了蛋提取物,能够组装线性.
- 使用不可降解形式和特定抑制剂操纵环林B水平和降解途径.
- 评估了这些操纵对MPF活动和姐妹染色体分离的影响.
主要成果:
- 为了启动姐妹染色体分离,不需要MPF失活.
- 抑制基因介导蛋白解,包括环林降解,延迟姐妹染色体的分离.
- 非环林蛋白的降解对于姐妹染色体链接的溶解是必要的.
结论:
- 乌比奎丁介导的蛋白质分解对于启动亚纳和姐妹染色体分离至关重要.
- 除了循环蛋白之外的蛋白质必须被降解以使姐妹染色体分离.
相关概念视频
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Microtubules form through the end-to-end polymerization of tubulin heterodimers. Kinetochore microtubules originate from the spindle poles, and their plus-ends connect with the kinetochores on sister-chromatids. Ndc80 protein complexes, present on the kinetochore, form low-affinity links with the plus end of these kinetochore microtubules.
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