MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom. Electronic address: https://twitter.com/StanislauY.
MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, United Kingdom.
Curr Opin Struct Biol. 2023 Aug;81:102638. doi: 10.1016/j.sbi.2023.102638. Epub 2023 Jun 20.
Kinetochores are large protein complexes built on centromeric chromatin that mediate chromosome segregation. The inner kinetochore, or constitutive centromere-associated network (CCAN), assembles onto centromeres defined by centromere protein A (CENP-A) nucleosomes (CENP-A), and acts as a platform for the regulated assembly of the microtubule-binding outer kinetochore. Recent cryo-EM work revealed structural conservation of CCAN, from the repeating human regional centromeres to the point centromere of budding yeast. Centromere recognition is determined mainly through engagement of duplex DNA proximal to the CENP-A nucleosome by a DNA-binding CENP-LN channel located at the core of CCAN. Additional DNA interactions formed by other CCAN modules create an enclosed DNA-binding chamber. This configuration explains how kinetochores maintain their tight grip on centromeric DNA to withstand the forces of chromosome segregation. Defining the higher-order architecture of complete kinetochore assemblies with implications for understanding the 3D organisation of regional centromeres and mechanisms of kinetochore dynamics, including how kinetochores sense and respond to tension, are important future directions.
动粒是构建在着丝粒染色质上的大型蛋白复合物,介导染色体分离。动粒的核心部分,或组成性着丝粒相关网络(CCAN),装配在由着丝粒蛋白 A(CENP-A)核小体(CENP-A)定义的着丝粒上,并作为微管结合的动粒外显子有规律地组装的平台。最近的冷冻电镜研究揭示了 CCAN 的结构保守性,从重复的人类区域着丝粒到出芽酵母的点状着丝粒。着丝粒的识别主要是通过位于 CCAN 核心的 DNA 结合 CENP-LN 通道与靠近 CENP-A 核小体的双链 DNA 近端的结合来确定的。其他 CCAN 模块形成的额外 DNA 相互作用形成一个封闭的 DNA 结合腔。这种构象解释了动粒如何保持对着丝粒 DNA 的紧密控制,以承受染色体分离的力。定义完整动粒组装的高级结构,对理解区域着丝粒的三维组织和动粒动力学机制具有重要意义,包括动粒如何感知和响应张力,这是未来的重要方向。