细胞分裂周期. 动态芯附着部被竞争性Mps1感知,微管与Ndc80C结合
Zhejian Ji1, Haishan Gao1, Hongtao Yu2
1Howard Hughes Medical Institute, Department of Pharmacology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 74390, USA.
概括
螺旋检查点可以防止细胞分裂中的错误. 单极旋1 (Mps1) 在微管结合部位与Ndc80复合体结合,检测未结合的动态,以防止动态化.
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:
- 螺旋检查点对于防止细胞分裂期间发生质积分至关重要.
- 核分裂循环80复合体 (Ndc80C) 是一个关键的微管受体在kinetochore和招募检查点蛋白质.
研究的目的:
- 研究检查点激酶Mps1与Ndc80复合体之间的直接相互作用.
- 阐明Mps1检测未连接的kinetochores的机制.
主要方法:
- 生物化学测试用于研究蛋白质与蛋白质相互作用.
- 在体外结合测试以评估Mps1-Ndc80C相互作用.
- 在人体细胞中进行功能测试,以评估检查点缺陷.
主要成果:
- 通过微管结合表面的两个独立相互作用,Mps1直接与Ndc80C结合.
- 微管与Ndc80C的结合抑制了Mps1的结合.
- 消除一个Mps1-Ndc80C相互作用会导致未连接的动脉检测有缺陷.
结论:
- 对于Ndc80C结合而言,Mps1和微管之间的竞争是感知未结合的kinetochore的直接机制.
- 这种相互作用对于通过防止形积分症来维持基因组稳定性至关重要.
更多相关视频
08:33Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
Published on: December 5, 2017
15.1K
12:26Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
Published on: May 3, 2018
19.5K
相关概念视频
Attachment of Sister Chromatids
4.2K
As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules. Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall...
4.2K
Attachment of Sister Chromatids
1.9K
1.9K
Forces Acting on Chromosomes
4.1K
During mitosis, chromosome movements occur through the interplay of multiple piconewton level forces. In prometaphase, these forces help in chromosome assembly or congression at the equatorial plane, eventually leading to their alignment at the metaphase plate. The forces acting on the chromosomes are space and time-dependent; therefore, they vary with the position of the chromosomes as the cell progresses through mitosis.
Microtubules and motor proteins exert two types of forces on...
Microtubules and motor proteins exert two types of forces on...
4.1K
Anaphase A and B
5.8K
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.
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
5.8K
Anaphase A and B
5.1K
5.1K
Spindle Assembly
4.5K
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
4.5K
